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A novel multifunctional coordination polymer {[Zn(HCOO) (bcbpy)Cl]·H 2 O} n (1) with multiple colour-changing has been synthesized from Zn(NO 3) 2 ·6H 2 O, and viologen ligand 1,1′-bis-((3-carboxylatobenzyl)-4,4′-bipyridinium) dichloride (H 2 bcbpy·2Cl). In coordination polymer (CP) 1 , bcbpy ligands bridge Zn2+ cations to form a 1D wave-like chain. CP 1 exhibited photochromic properties under xenon lamp and blue light irradiation while obtaining a structurally stable light product 1T. CP 1 thermochromic properties can also be observed during heating. 1 showed photo-controlled fluorescence properties during color rendering and decolorization, and its properties were studied. Interestingly, CP 1 can be deposited in filter paper by coating it with a solution of H 2 O. The filter paper can be used as a printing medium without ink. [Display omitted] • CP 1 was synthesized using viologen ligand 1,1′-bis-((3-carboxylatobenzyl)-4,4′-bipyridinium) dichloride (H 2 bcbpy·2Cl). • CP 1 exhibited photochromic properties under xenon lamp and blue light irradiation. • CP 1 obtaining a structurally stable light product 1T after irradiation. • CP 1 can be used as a good ink-free printing medium. [ABSTRACT FROM AUTHOR]

Two novel cyanostilbene-modified tetraphenylethene derivatives were constructed by Williamson etherification, Suzuki coupling and Knoevenagel condensation reactions. Both compounds exhibited aggregation-induced emission and strong solid-state fluorescence behaviors with extremely high fluorescence quantum yield due to the distorted molecular conformation. Strangely, the compound without additional phenyl spacer did not show mechanochromic behavior, whereas, the compound with an additional phenyl spacer exhibited distinct mechanochromic behavior with the red-shifted emission wavelength from 480 nm to 503 nm upon grinding. The distinct differences in mechanochromic behaviors between the reported compounds could be attributed to that the additional phenyl spacer had benefits for the molecular planarization with external mechanical force. This investigation provided a method to construct mechanochromic material with aggregation-induced emission behavior and high solid-state fluorescence quantum yield and promoted the utilization in rewritable luminescent paper. Two novel AIE-active cyanostilbene-modified tetraphenylethene derivatives were prepared and the additional phenyl spacer induced distinct AIE behaviors, solid-state fluorescence and mechanochromic behaviors. [Display omitted] • Two novel AIE-active cyanostilbene-modified tetraphenylethene derivatives were obtained. • The incorporation of phenyl induced different solid-state fluorescence with high fluorescence quantum yield. • The incorporation of more phenyl induced big difference in mechanochromic behavior. [ABSTRACT FROM AUTHOR]

Multistimuli responsive materials based on the viologen coordination polymers have attracted much interest in the past few years due to the increasing demand for smart materials. In this paper, based on a viologen ligand 1-(3-carboxybenzyl)- 4,4′-bipyridinium chloride (Hcbbpy) and zinc(II) ion, a new crystalline complex, namely, {[Zn(cbbpy)Cl 2 ]·H 2 O} n (1) has been designed and synthesized. In complex 1 , every cbbpy ligand as a bridge links two Zn2+ ions via carboxylate O atom and pyridine N atom to extend to a 1D zigzag chain. The 1D chains are extended to 3D supramolecular structure through π···π stacking and hydrogen bonding. More importantly, 1 exhibits fast photochromic behaviors in response to UV and X-ray due to the formation of viologen radicals. Complex 1 also shows photo-modulated luminescence property in the solid state. In addition, complex 1 can be deposited on filter paper and displays the potential application as inkless print material. [Display omitted] • A new viologen complex was successfully synthesized and characterized. • Complex 1 shows fast response to UV light and X-ray irradiation. • Complex 1 can be deposited on filter paper and displays as inkless print material. [ABSTRACT FROM AUTHOR]

In this paper, the crystal structure, physical properties, photoelectric conversion efficiency and large-area development of CsPbI 3 all-inorganic perovskite solar cells are comprehensively analyzed. The research results of the material in photoelectric conversion efficiency, large-area development and preparation technology are summarized. In addition, through theoretical prediction and simulation, this study simulated a CsPbI 3 all-inorganic perovskite solar cell with a photoelectric conversion efficiency of 28.29 %, which provided a theoretical basis for the preparation of high-performance devices. In this paper, the physical properties, photoelectric conversion efficiency, large area and preparation methods of CsPbI 3 all-inorganic perovskite solar cells are summarized in detail. In addition, the theoretical efficiency of the device was predicted, and the CsPbI 3 all-inorganic perovskite solar cell with a theoretical photoelectric conversion efficiency of 28.29 % was successfully obtained. [Display omitted] • CsPbI 3 all-inorganic perovskite solar cells. • Physical Properties of CsPbI 3 Materials. • Research status and preparation methods. • The theoretical efficiency of simulation prediction reaches 28.29 %. • Challenge and strategies. [ABSTRACT FROM AUTHOR]

The encapsulation of photoactive guests into a metal-organic framework is advantageous in endowing extra functionalities such as photochromism and photoswitchable luminescence. In this paper, a host-guest MOF material, [Zn 3 (IPA) 4 ​MV] (1) (H 2 IPA ​= ​isophthalic acid, MV·2NO 3 ​= ​1,1'-dimethyl-(4,4'-bipyridine)-1,1'-diium dinitrate) has been constructed by encapsulating simplest methyl viologen guest into the anionic MOF framework. This material exhibits reversible naked-eye detectable photochromic properties varying from colorless to blue upon UV–Vis light irradiation. The MV2+ and the short O⋯N distance between the oxygen atom and pyridine ring of MV2+ play a crucial role in the photochromism of this compound. This host-guest MOF compound shows photoswitchable luminescent properties in the solid state. More interestingly, this host-guest MOF material can be deposited on filter paper and can be employed as inkless print material by controlling the UV–Vis light irradiation with the stencil. A novel MOF-based host-guest compound was prepared by incorporating the photoactive methyl viologen into the anionic framework, which exhibit photochromism upon UV–Vis light irradiation and photocontrolled luminescence. Moreover, this compound can be used as inkless and erasable print media. [Display omitted] • A host-guest compound was prepared by incorporating the viologen into the anionic MOFs. • Compound 1 exhibits fast-responsive photochromism and reversible luminescence switching upon UV–Vis light irradiation. • Compound ​ 1 ​can be employed as inkless and erasable print media by controlling the UV-Vis light irradiation. [ABSTRACT FROM AUTHOR]

Eu3+ and Tb3+ as central ions and 1,4-phthalic acid (H 2 BDC) as ligand, a dual lanthanide metal-organic framework, Eu-Tb(BDC), was synthesized by co-precipitation method. The products performed stable crystal structure and adjustable fluorescence color. Eu 0.15 Tb 2.85 (BDC) 3.0 was selected as an optimized probe to detect norfloxacin (NFX) in urine, and the fluorescence color was found to transfer from bright yellow to dark cyan and then to strong green with increasing NFX concentration. Mechanism analysis revealed that NFX with low concentration (10−6-10−3 M) stimulated light competition with BDC ligand due to internal filtration effect (IFE), resulting in the gradual fluorescence shutdown of Eu3+and Tb3+. While further increasing concentration of NFX to 10−3-10−2 M, the antibiotic molecules coordinated with lanthanide ions and transitioned their role from competitor to assistant. Where the energy transfer due to antenna effect overwhelmed IFE, the exciting light energy were retransferred to Eu3+ or Tb3+, and the probe's fluorescence restored. Generally, the Eu-Tb(BDC) probe performed fluorescence turn off-on response to norfloxacin with continuous concentration changing. Additionally, when detecting other fluoroquinolone antibiotics, the fluorescence of Eu 0.15 Tb 2.85 (BDC) 3.0 changed from bright yellow to bright blue and eventually to dark red, which was attributed to the different coordination degrees of various antibiotic molecule with Tb3+ and Eu3+. It can be used to distinguish norfloxacin from other fluoroquinolone antibiotics. Synthesis route of Eu-Tb(BDC) and its fluorescence sensing mechanism and application of test paper visualization. [Display omitted] • Europium-terbium co-doped metal-organic framework was prepared by coprecipitation method and applied to test paper. • Eu-Tb(BDC) can quantitatively sense and distinguish between norfloxacin and other fluoroquinolone antibiotics. • The phenomenon of fluoroquinolone antibiotics turning off to Turn on has been discussed. [ABSTRACT FROM AUTHOR]

Azo dyes are difficult to degrade, dark in color and toxic in the aqueous environment, which will harm the ecological environment and human health if left untreated. Photocatalytic technology has a wide range of applications in the treatment of printing and dyeing wastewater; in the present study, nano Zr–BiOI/GO photocatalytic composites were prepared by a hydrolysis method using Bi(NO 3) 3 –5H 2 O and ZrOCl–8H 2 O as precursors and GO as carriers. The structure and properties of the samples were characterized by combining test methods such as XRD, FESEM, TEM, XPS, and UV–vis. Congo red (CR) was used as the target pollutant to assess the photocatalytic performance of the prepared materials. The results showed that the specific surface area of 10 % Zr–BiOI/GO increased from 21.98 m2/g to 152.79 m2/g, and the average particle size decreased from 21.61 nm to 17.75 nm compared with that of BiOI. Compared with BiOI, the light-absorption threshold of 10 % Zr–BiOI/GO was increased from 640.6 to 726.4 nm, and the forbidden bandwidth was decreased from 1.94 eV to 1.71 eV. In addition, the nanocomposites exhibited excellent stability and removal of organic dyes and could be used as a potential photocatalyst for water remediation under visible light. The removal of CR by 10 % Zr–BiOI/GO composite was 95.42 % at 120 min. The photocatalytic degradation process of Zr–BiOI/GO conformed to the first-order kinetic model, and the correlation coefficient of the kinetic curve of 10 % Zr–BiOI/GO was 0.9465 and the reaction rate constant was the greatest at 0.0221 min−1. Superoxide radicals [·O 2 −] play a major role in photocatalytic activity. The results indicate that nanocomposites are a promising candidate for photocatalytic degradation of water pollutants. In this paper, Zr–BiOI/GO photocatalytic composites were prepared by a simple hydrolysis method, which possessed higher specific surface area and narrower forbidden bandwidth than pure BiOI, and could remove up to 95.42 % of Congo red (CR) solution under visible light, in addition to the high stability and recycling rate of Zr–BiOI/GO. [Display omitted] • The pore structures of Zr–BiOI/GO photocatalytic materials prepared by hydrolysis method were well developed. • The maximum removal of Congo red by mesoporous Zr–BiOI/GO photocatalytic material was 96.84 %. • Paradigm of Zr–BiOI/GO resource recovery and wastewater treatment was provided. • Long-term experiments were conducted with excellent stability. [ABSTRACT FROM AUTHOR]

Volatile organic compounds (VOCs) not only pollute the environment, but also seriously damage human health. Studies have shown that CeO 2 doped with Cr and other metal elements can significantly improve its catalytic activity. In this paper, MIL-101 (Cr) was selected as the precursor of Cr 2 O 3 , and x wt%Cr 2 O 3 /CeO 2 catalysts (x = 5, 10, 15) with different loadings were prepared by impregnation method. The physicochemical properties of the catalysts were characterized by XRD, SEM, BET, XPS and H 2 -TPR, and their catalytic performance was evaluated by toluene catalytic combustion. The results show that 10 wt%Cr 2 O 3 /CeO 2 exhibits the best catalytic activity for toluene combustion, and the conversion of toluene can reach 90% at 263 °C. This can be attributed to the relatively high specific surface area (118 m2 g−1), the highest surface adsorbed oxygen content (O ads /O total = 0.251), oxygen vacancy content, more surface Ce3+ species and Cr6+ species, and the best low-temperature reducibility. [Display omitted] • In this paper, MIL-101 (Cr) was selected as the precursor of Cr 2 O 3 , and x wt%Cr 2 O 3 /CeO 2 catalysts (x = 5, 10, 15) with different loadings were prepared by impregnation method. • The 10 wt%Cr 2 O 3 /CeO 2 exhibits the best catalytic combustion activity of toluene, with the lowest E a value, and the conversion of toluene can reach 90% at 263 °C. • The 10 wt%Cr 2 O 3 /CeO 2 has a relatively high specific surface area (118 m2 g−1), the highest surface adsorbed oxygen content, oxygen vacancy content, more surface Ce3+ species and Cr6+ species, and the best low-temperature reducibility, so it has good catalytic activity. [ABSTRACT FROM AUTHOR]

Cost-effective and efficient capture of Cs+ ions from radioactive wastewater is crucial for the sake of environmental protection and human health but full of challenges. In this paper, we present the suitability of a layered metal sulfide, namely Na 2 Sn 3 S 7 (NaTS), for the remediation of cesium by ion exchange, with the merits of facile preparation, cheap composition, high efficiency and good selectivity. The cesium adsorption behaviors including kinetic time, saturation capacity, pH values, interfering ions, dose and recyclability were explored in detail. The experimental results show that it has a fast cesium uptake kinetics (ca. 60 min), with a maximum adsorption capacity of 140.32 mg/g and a wide pH resistance of 2.2–12.6. Also, it exhibits the strong affinity for low-level Cs+ ion even in the presence of excessive Na+/Ca2+ ions, actual water environment and the dose-related researches, with the highest distribution coefficient K d value reaching 9.61 × 103 mL/g. More importantly, the cesium adsorption performances in the recycling study and the flow membrane-like filtration application are still impressive. These advantages demonstrated by NaTS render it very promising for the inexpensive and effective incarceration of aqueous cesium. Presented is the potentiality of an economically friendly and facilely synthesized layered metal sulfide for efficient removal of aqueous cesium. [Display omitted] • NaTS has the inexpensive component and the facile preparation process. • NaTS possesses a fast cesium uptake kinetics with a large capacity and wide pH resistance. • NaTS exhibits the strong affinity for the low-level Cs+ ion. • NaTS also demonstrates the potential in the flow membrane-like filtration application. [ABSTRACT FROM AUTHOR]

Vibration energy can be seen everywhere in our daily life, such as walking, noise and car engines. If all this energy could be captured and harnessed, it would be an interesting breakthrough in energy. This has been made possible by the discovery of piezoelectric materials, which can convert vibrational energy into electricity by sensing positive and negative charges. In this paper, nickel butadione oxime Ni(dmgH) 2 and strontium titanate (SrTiO 3) were successfully combined together to form the composite material of nickel butadione oxime/strontium titanate SrTiO 3 /Ni(dmgH) 2 by hydrothermal method. The morphology and composition of the sample were analyzed by XRD, SEM and XPS characterization methods. Strontium titanate and nickel butadione oxime were successfully combined with good crystallinity. According to the degradation results of HTC solution, the piezoelectric catalytic performance of the dye can be significantly improved in a specific time, and the degradation efficiency of HTC solution reaches about 91 %. Compared with the pure Ni(dmgH) 2 , the composite sample shows better piezoelectric catalytic activity under ultrasonic vibration. A novel SrTiO 3 /Ni(dmgH) 2 composite piezoelectric material was synthesized by hydrothermal method. The addition of SrTiO 3 promotes the separation of electrons and holes, and the piezoelectric catalytic activity is significantly improved. Compared with pure Ni(dmgH) 2 , the composite exhibited better piezoelectric catalytic activity under ultrasonic vibration. [Display omitted] • The piezoelectric catalyst SrTiO 3 /Ni(dmgH) 2 was synthesized by simple hydrothermal method. • The addition of SrTiO 3 facilitates the separation of electrons and holes. • SrTiO 3 /Ni(dmgH) 2 has excellent piezoelectric catalytic HTC performance. • SrTiO 3 /Ni(dmgH) 2 has good stability and reusability. [ABSTRACT FROM AUTHOR]

In this paper, we have presented the comprehensive characterization of red-light-emitting novel β-BaB 2 O 4 : x Sm3+ (x = 0.5, 0.75, 1, 1.5, and 2 mol%) phosphor samples synthesized by making use of solid-state reaction method. The XRD patterns verified the successful synthesis and in-depth analyses were carried out to explore the structural, luminescence, and thermal properties. Notably, the introduction of Sm3+ through doping did not result in any substantial alterations in the crystal structure. Photoluminescence (PL) emission spectra exhibited 4 distinct peaks for 401 nm excitation. Out of these 4 peaks, the prominent peak was present at 601 nm, attributed to the magnetic dipole-allowed transition 4G 5/2 → 6H 7/2. The colorimetric analysis revealed the correlated color temperature (CCT) to be around 1700 K, accompanied by 99.9 % colour purity. The optimal doping concentration, before luminescence quenching, was identified as 1 mol%, with multipole-multipole interactions identified as the predominant quenching mechanism. Diffuse reflectance spectroscopy (DRS) studies on β-BaB 2 O 4 :1%Sm3+ confirmed characteristic peaks corresponding to Sm3+ transitions, revealing an ionic bonding nature between Sm3+ and the host. Also, the direct optical band gap was determined to be 5.62 eV. Furthermore, the optimized phosphor demonstrated exceptional temperature-dependent photoluminescent (TDPL) properties, exhibiting a negligible (∼5 %) decrease in emission intensity for prominent peaks even at 440 K. Overall, the phosphors displayed high activation energy, significant thermal stability, and thermal sensing properties, making them promising candidates for various optoelectronic applications. [Display omitted] • Sm3+ doped -BaB 2 O 4 phosphors have been successfully synthesized via solid-state reaction method. • XRD and FTIR revealed that the structural properties of the phosphor were not affected by the doping. • The prepared phosphor exhibited reddish-yellow emission and excellent temperature-dependent PL spectra. • Optimally optimized phosphor was thermally stable and exhibited TDPL spectra up to a temperature of 443 K. • Due these features, the phosphor is a worthy candidate for light emission, WLED, and thermal sensing applications. [ABSTRACT FROM AUTHOR]

As a new member of the carbon family, γ-graphyne is combined with SrTiO 3 for the first time in this paper, and a series of SrTiO 3 /γ-graphyne heterostructures are synthesized by a simple impregnation method. The as-prepared heterostructures are investigated by a series of characterizations, and the optimal content of γ-graphyne (γ-GY) is determined to be 1.0 wt%. After γ-GY modification, the maximum photocurrent and current density are enhanced by 30 and 5 folds, respectively, and the excitation and separation of photogenerated charges enhanced. In addition, the degradation of methylene blue by the heterostructured SrTiO 3 /γ-graphyne under visible light irradiation reached 88 % in 30 min with a photocatalytic rate of 6.277 × 10−2min−1, enhanced by 3.04 times compared with SrTiO 3. The degradation properties are also proved by Rhodamine B degradation tests. The excellent stability and recyclability of the catalysts are proved. And h+, •O 2 −, and •OH are demonstrated to play roles in the reaction process, with •OH being the main active substance. A possible photocatalytic mechanism is further suggested. This work sheds light on the design of γ-GY modified composites for photoelectrochemical and photocatalytic applications. [Display omitted] • The 2D γ-graphyne is assembled onto SrTiO 3 particles by simple wet impregnation and stable heterojunctions are formed. • The SrTiO 3 /γ-GY composites are characterized by high photoelectrocatalytic activity and exhibit excellent photocatalytic performance for MB photodegradation tests. • The successful combination of γ-GY and SrTiO 3 expands light absorption range and reduces carrier recombination. • γ-graphyne nanosheets provide fast transfer channels and electron sinks for carrier migration and separation. [ABSTRACT FROM AUTHOR]

Solid-state electrolytes for sodium batteries have been studied for many years, however, have not advanced much since at ambient temperature solid-state electrolytes still exhibit a magnitude huge gap in ionic conductivity than the commercial organic liquid electrolytes. In this paper, the solid-state electrolyte Na 5 YSi 4 O 12 (NYS) is synthesized employing the solution-assisted solid-state reaction (SASSR) method with the ionic conductivity (σ t) reaching up to 1.52 mS cm−1 sintered at 1050 °C for 6 h, demonstrating a significant progress improvement over the conventional solid-phase reaction method. On this basis, Y3+ is further substituted with the other Lanthanides including Yb3+, Dy3+, Gd3+, Eu3+, and Sm3+ to form the solid electrolytes Na 5 MSi 4 O 12 (M = Yb3+, Dy3+, Gd3+, Eu3+, and Sm3+). The conductivity evolution is found increasing with the increase in the ionic radius of the substituted elements. The X-ray diffractometer analysis reveals a wider sodium ion transport channel and larger ionic radius which lead to higher sodium ion concentration. However, the sintering temperature and impurity phase are reduced with an increase in ionic radius. Notably, among the six solid-state electrolytes, Na 5 SmSi 4 O 12 (NSS) exhibits the highest conductivity of 2.41 mS cm−1 and the lowest sintering temperature of 950 °C. The low sintering temperature and high ionic conductivity make NSS a fast sodium conductor that can meet industrial needs. [Display omitted] • The solution-assisted solid-state reaction was used to synthesize Na 5 YSi 4 O 12. • The conductivity of Na 5 YSi 4 O 12 can reach 1.52 mS cm−1 at room temperature. • Lanthanides Yb3+, Dy3+, Gd3+, Eu3+and Sm3+ were substituted for Y3+ in Na 5 YSi 4 O 12. • Na 5 SmSi 4 O 12 exhibits the highest conductivity of 2.41 mS cm−1. • XRD revealed that enhancing the ionic radius of Lanthanides increased the Na + transport channel. [ABSTRACT FROM AUTHOR]

Single-crystal-to-single-crystal (SCSC) transformation provides a good platform for obtaining new functional coordination polymers. In this study, we demonstrate a violent and rapid structural transformation between two d10 coordination polymers (CPs). The complex 1 [Zn(3,5-thbzc) 2 (C 2 H 6 O) 2 ] transformed into the complex 2 {[Zn(3,5-thbzc) 2 (H 2 O) 2 ]·C 3 H 7 NO·2H 2 O} (where t = tbutyl, hbzc− = 2-Hydroxybenzoato) triggered by deionized water under standard temperature and pressure conditions in solid state. The transformation reaction was confirmed using single-crystal XRD, PXRD and SEM. The results showed that complex 1 adopts a bidentate chelate six-coordination mode, and complex 2 adopts a monodentate four-coordination mode. SEM clearly showed that complex 2 was in the form of random nanowire clusters, suggesting that their transformation required degradation of the entire crystal structure. UV–Vis–NIR spectra were used to calculate the band gaps of complexes 1 and 2 , which demonstrated wide-bandgap semiconductor-like materials with ∼3.2 eV band gap widths. The results of dielectric studies of complex 1 revealed that it possessed a medium dielectric constant (κ = 6.08 at 1 kHz), while complex 2 displayed an even higher dielectric constant (κ = 7.97 at 1 kHz) at room temperature. Interestingly, parent complex 1 exhibited a small ladder-like dielectric anomaly at 188 °C, while progeny complex 2 did not. This paper describes a new strategy for preparing adjustable functional dielectric materials. Through solid-state transformation triggered by deionized water, the parent bidentate six-coordination complex 1 generates the progeny monodentate four-coordination complex 2. This transformation process involves the cleavage and regeneration of coordination bonds. Complex 2 has a high dielectric constant due to the substitution of water ligands. [Display omitted] • Ligand-substituted SCSC transformation between complexes 1 and 2 was triggered by deionized water. • The transformation process involves the cleavage and regeneration of coordination bonds. • The coordination number of Zn2+ changes from six-coordination to four-coordination. • The introduction of H 2 O ligands can significantly improve the dielectric constants of Zn-CPs. • Complex 1 shows a ladder-like dielectric anomaly at 188 °C. [ABSTRACT FROM AUTHOR]

Photocatalytic Hydrogen production as one of the effective ways to solve the future energy issues has recently become a research hotspot in the field of renewable energy. However, single-component photocatalysts have poor hydrogen production efficiency due to the narrow light-absorption range, susceptibility to photo-corrosion and low catalytic activity. Herein, novel heterojunction photocatalysts of ZnIn 2 S 4 @BiYWO 6 with different mass ratios were designed and synthesized using a facile two-step hydrothermal method. Experimental results and analyses show that these heterojunction catalysts exhibit extremely excellent photocatalytic performance for hydrogen production. Especially, the hydrogen production rate of 10ZnIn 2 S 4 -BiYWO 6 is 73 times higher than that of pure ZnIn 2 S 4. Furthermore, enhanced photocatalytic mechanism and carrier transfer pathway in the heterojunction photocatalyst of ZnIn 2 S 4 @BiYWO 6 were deeply analyzed and explored in the paper, which confirmed that ZnIn 2 S 4 @BiYWO 6 is a direct Z-scheme heterojunction architecture. Within such a Z-scheme framework, the presence of a built-in electric field at the interface between ZnIn 2 S 4 and BiYWO 6 as well as the energy band bending lead to the direct recombination of electrons and holes with low redox capacity, while keeping the electrons and holes with high redox capacity in each component. Consequently, the photocatalytic activity of the Z-scheme heterojunction system has been greatly enhanced. It is believed that the present work provides valuable guidance for the design and construction of novel Z-scheme heterojunction photocatalysts. Z-scheme heterojunctions greatly enhanced photocatalytic hydrogen production efficiency of ZnIn 2 S 4 @BiYWO 6 composites. [Display omitted] • ZnIn 2 S 4 @BiYWO 6 photocatalysts exhibit excellent hydrogen production efficiency. • Z-scheme heterostructures play a key role in enhancing photocatalytic activity. • Such Z-scheme photocatalysts are promising for photocatalytic hydrogen production. [ABSTRACT FROM AUTHOR]

In this paper, the glass forming region of TeO 2 –MoO 3 –Nb 2 O 5 (TMN) tellurite glass and the luminescence properties of Er3+ doped TMN glass at 2.7 μm were studied. The effects of MoO 3 on the thermal and optical properties of the glass were analyzed. The formation region of TMN glass was predicted by thermodynamic method and verified by experiment. It can be found that the glass-forming ability, thermal and optical properties of TMN glass change significantly with the change of MoO 3 content. The addition of MoO 3 significantly improves the anti-crystallization stability, fluorescence lifetime and quantum efficiency of tellurite glass. The calculation results show that the quantum efficiency of 80TeO 2 –15MoO 3 –5Nb 2 O 5 –1Er 2 O 3 glass sample is 16 %. These results indicate that TMN glass has a broad application prospect in mid-infrared laser materials. The formation region of TMN glass was predicted and experimentally verified using thermodynamic methods. The effects of MoO 3 on the luminescence properties and quantum efficiency of the tellurite glass were analyzed. The results show that the addition of MoO 3 significantly improves the glass-forming properties and quantum efficiency of tellurite glass. [Display omitted] • The formation region of TMN tellurate glass was predicted and verified. • The prepared glasses have high quantum efficiency in 2.7 μm emission. • The prepared glasses have a large emission cross-section of 2.7 μm emission. • The modest introduction of MoO 3 will improve quantum efficiency. [ABSTRACT FROM AUTHOR]

The structure and properties of basic metal-organic frameworks (MOFs) continue to exhibit low Cd(II) uptake and selectivity. Assembly of same zinc-based MOF building blocks into a dual-zinc MOF@MOF composite could offer a promising avenue for efficiently capturing Cd(II) from aqueous solutions. This paper reports a dual-zinc MOF@MOF (Zn-BTC@ZIF-8, DZM) adsorbent, which was constructed for boosting the performances of adsorption and separation. The adsorption behavior of Cd(II) onto DZM from aqueous solution is thoroughly examined at room temperature. Results indicates that the DZM demonstrates significant capability in capturing Cd(II), attributed to the synergistic effects of Zn-BTC and ZIF-8 with diverse active sites, appropriate pore sizes and shapes, stable dual zinc bonding interaction, and more. The maximum Cd(II) uptake capacity reached 150 mg/g, with rapid attainment of adsorption equilibrium within just 20 min, surpassing the performance of other reported adsorbents in the literature. The adsorption data align well with both the Freundlich and pseudo-second-order kinetic models. The process of adsorption is a process of spontaneous heat absorption and increasing degrees of freedom. Particularly noteworthy is the sustained effectiveness of DZM in capturing Cd(II) even after the fifth cycle. This research introduces a fresh approach to crafting desirable MOF@MOF configurations, thereby advancing their potential utility in Cd(II) removal from water. [Display omitted] • A new-style dual-zinc MOF@MOF (Zn-BTC@ZIF-8) adsorbent was first constructed. • The Zn-BTC@ZIF-8 composite exhibits adsorption performance toward Cd(II). • Double MOF structure is beneficial to expose more active sites and facilitate Cd(II) capture. [ABSTRACT FROM AUTHOR]

In this work, the hydrothermal method was employed to synthesize the nickel vanadate microspheres (NVO MSs), an effective catalyst for supercapacitor and water-splitting applications. Specifically, X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, and Brunauer-Emmett-Teller (BET) were used to examine the crystal structure, surface morphology, functional group identification, the stretching-bending vibration of the N–V–O group, and the specific surface area respectively. Additionally, this paper reports the electrochemical aspects of NVO MSs in various concentrations of KOH electrolyte using nickel foam (NF) as a current collector. As a result, the NVO-NF 1 electrode exhibited excellent electrochemical activity with a higher specific capacitance (C s) and capacity (C sp) of 959 F/g and 119 mAh/g at a current density of 5 mA/g respectively. Moreover, the NVO-NF 1 electrode delivers maximum energy (E d) and power density (P d) of 26 Wh/kg and 1100 W/kg and excellent stability with 90 % retention after 4000 CV cycles. In the asymmetric liquid state device (ASC), the NVO-NF acts as a cathode, and activated carbon (AC) as a anode materials respectively. Furthermore, the fabricated ASC device reveals maximum E d and P d of 47 Wh/kg and 2300 W/kg at 5 mA/g and also demonstrated superior stability over 5000 cycles. Furthermore, the significant finding of the NVO-NF 1 electrodes reveals superior electrocatalytic activities such as the lowest value of overpotential (234 mV), with the sufficient Tafel slope (73 mV/dec), as well as the maximum electrochemical active surface area (670.5 cm2) in 1 M KOH at 10 mA/cm2 respectively. As a result, better performance of the NVO-based MSs in 1 M KOH electrolyte was effectively applied to power effective electrodes for energy storage and water-splitting. Scheme: Schematic illustration for the electrochemical and electrocatalytic activities of the NVO electrodes in the aqueous KOH electrolyte. [Display omitted] • Hydrothermal method was used for preparing Ni 2 V 2 O 7 MSs for SCs and WS application. • The interconnected microsphere-like morphology was observed for NVO material. • The performance of NVO electrodes was checked using various conc. of KOH. • The ACS device (NVO–NF//AC-NF) shows better electrochemical performance. • As a result, NVO-NF 1 shows good electrochemical and electrocatalytic activities. [ABSTRACT FROM AUTHOR]

In this paper, a Z-type heterojunction is formed between BiOI and Ni doped MoS 2 by hydrothermal and microwave-assisted methods. The composites were characterised by a range of characterisation methods. The test results show that the formation of heterojunction can reduce the forbidden bandwidth of the material and improve the absorption of visible light, and the photocatalytic performance can be improved. The degradation efficiency of 5 % BiOI/Ni 0.05 Mo 0.95 S 2 against 150 mg/L rhodamine B was 95.08 % in 300 min. The analysis of first-principles calculations reveals that BiOI will hybridise with Ni 0.05 Mo 0.95 S 2 at the energy level, leading to a decrease in the forbidden bandwidth of the composite. The difference in the figure of merit of the two materials favours the reduction of the photogenerated carrier complexation rate, which is conducive to the enhancement of the photocatalytic performance. This research uses impurity energy levels and heterojunctions together on catalytic materials to improve their catalytic properties which has far-reaching implications for future research on environmental issues. BiOI was chosen to form heterojunctions by microwave-assisted compounding with Ni 0.05 Mo 0.95 S 2 to achieve degradation of high rhodamine B concentrations under visible light. [Display omitted] • BiOI/Ni0.05Mo0.95S2 composites were prepared by the microwave-assisted method. • In 300 min of 150 mg/L RhB, the degradation efficiency of 5% BiOI/Ni 0.05 Mo 0.95 S 2 was 95.08%, and the reaction rate constant was 1.095 times that of Ni 0.05 Mo 0.95 S 2. • Trap tests on the composites indicate that the main reactive group in the photocatalytic degradation of RhB is h+. • First-principles calculations have shown that the formation of heterostructures of BiOI and Ni 0.05 Mo 0.95 S 2 can facilitate charge transfer and favorably improve photocatalytic efficiency. [ABSTRACT FROM AUTHOR]

With high hydrothermal stability and hydrophilicity, MIL-100(Fe) has potential applications in sorption-based atmospheric water harvesting (SAWH). This paper reports the water vapor adsorption properties of MIL-100(Fe) prepared by solvent and solvent-free methods. Performance tests show that the MIL-100(Fe) prepared by solvent-free method has more advantages. To further improve the performance of the adsorbent, the composite adsorbent MgCl 2 @MIL-100(Fe) was obtained by impregnating MIL-100(Fe) with MgCl 2 solution. The results showed that the composite adsorbent had good adsorption performance, desorption properties, and fast adsorption rate. The equilibrium adsorption capacities of the composite adsorbent with 35% salt content were 0.533 g/g and 1.062 g/g at 25 °C with the relative humidity (RH) of 35% and 80%, respectively, which were 1.51 times and 1.74 times of the adsorption capacity of MIL-100(Fe) under the same working conditions. This showed that the solvent-free synthesized MIL-100(Fe) and its composite adsorbent have the potential for application in SAWH. This paper compares the solvent-free synthesis of MIL-100(Fe) with the hydrothermal synthesis of MIL-100(Fe) with solvent. Then, by evaluating the various properties (characterizations, adsorption performance, cycle stability, preparation cost, etc.) of materials prepared by two different methods, it is determined whether the MIL-100(Fe) prepared by the solvent-free synthesis method is more suitable for water vapor adsorption. Eventually, to further improve the adsorption performance of this material, MIL-100(Fe) was impregnated in MgCl 2 solution to develop a new composite adsorbent MgCl 2 @MIL-100(Fe) for further study. [Display omitted] • The solvent-free synthesized MIL-100(Fe) has excellent adsorption performance and cycle stability. • The composite adsorbent MgCl 2 @MIL-100(Fe) has rapid adsorption kinetics. • The adsorption capacity of the composite adsorbent with an MgCl 2 mass fraction of 35% can reach 1.062 g/g. • The composite adsorbent has good water absorption at low relative humidity, which can reach 0.533 g/g. [ABSTRACT FROM AUTHOR]

In this paper, a kind of zero valent FeNi alloy nano powder was coated on the surface of SrFe-MOF powder by a simple, efficient and pollution-free method, forming a core-shell type FeNi p @SrFe-MOF Magnetic powder (FSM). The FSM powder has a porous structure and a specific surface area of 9.16 ​m2/g. Under normal temperature and without changing the pH value of the wastewater, the FSM magnetic powder has an immediate and efficient removal effect on Congo Red (CR) dye wastewater. Furthermore, the powder has good cycling performance, with the CR removal rate remaining above 90% after five cycles. Also at room temperature and without changing the pH value of the wastewater, the FSM magnetic powder provides some immediate, efficient, and repeated use degradation of Cr(VI) wastewater. The FSM magnetic powder has good magnetic properties so that can be easily separated and recovered by magnetic field treatment, which solves the problem of efficient recovery of raw materials in wastewater treatment. FSM magnetic powder has broad application prospects for treating wastewater. In this paper, a kind of zero valent FeNi alloy nano powder was coated on the surface of SrFe-MOF powder by a simple, efficient and pollution-free method, forming a core-shell type FeNi p @SrFe-MOF Magnetic powder (FSM). Under normal temperature and without changing the pH value of the wastewater, the FSM magnetic powder has an immediate and efficient removal effect on Congo Red (CR) dye wastewater. Furthermore, the powder has good cycling performance, with the CR removal rate remaining above 90% after five cycles. Also at room temperature and without changing the pH value of the wastewater, the FSM magnetic powder provides some immediate, efficient, and repeated use degradation of Cr(VI) wastewater. The FSM magnetic powder has good magnetic properties so that can be easily separated and recovered by magnetic field treatment. [Display omitted] • FSM powder has an immediate and efficient removal effect on CR at room temperature and without changing the pH value of the wastewater. • FSM powder has some removal effect on Cr(VI) at room temperature and without changing the pH value of the wastewater. • FSM powder has good magnetic properties, which can be separated and recycled by magnetic field treatment. [ABSTRACT FROM AUTHOR]

The design of a simple and efficient fluorescent probe for detecting hypochlorite (ClO−) is of great importance. Herein, we synthesized the hydroxyl-functionalized UiO-66 (UiO-66-(OH) 2) by the solvothermal method and its derivative aluminium ion-modified UiO-66-(OH) 2 (Al3+@UiO-66-(OH) 2) as two fluorescence probes are used for detecting ClO− in the water. The results showed that UiO-66-(OH) 2 has excellent fluorescent response ability for ClO− in water. Aluminium ion-modified UiO-66 (Al3+@UiO-66-(OH) 2) displayed its high efficiency for the fluorescence detection of ClO− with a response time of 30 ​s and extraordinary limit of detection of 1.63 ​μM in water. Moreover, the sensing of ClO− using easily portable Al3+@UiO-66-(OH) 2 -coated paper strips is also developed. Furthermore, the plausible fluorescence sensing mechanism of UiO-66-(OH) 2 for ClO− in aqueous solution was also discussed. Hydroxyl-functionalized and Al3+-modified UiO-66 for detecting ClO− are proposed.UiO-66-(OH) 2 and Al3+@ UiO-66-(OH) 2 shows superior fluorescence intensity. Moreover, Al3+@ UiO-66-(OH) 2 sensor shows highly sensitive and selective to detect ClO-. Portable Al3+@UiO-66-(OH)2-coated paper strips are developed for detecting ClO. [Display omitted] • Hydroxyl-functionalized and Al3+-modified UiO-66 for detecting ClO− are proposed. • UiO-66-(OH) 2 and Al3+@ UiO-66-(OH) 2 shows superior fluorescence intensity. • Al3+@ UiO-66-(OH) 2 sensor shows highly sensitive and selective to detect ClO-. • Portable Al3+@UiO-66-(OH) 2 -coated paper strips are developed for detecting ClO−. [ABSTRACT FROM AUTHOR]

Glutamic acid (Glu) is a biomarker of some neuropathological diseases, whose detection is of significance in early medical diagnosis. A 3D terbium metal-organic framework (Tb-ddb) is constructed from 1,3-di(3′,5′-dicarboxylphenyl)benzene (H 4 ddb) with Tb3+, displaying the 5D 4 → 7F j (j = 6-3) transfers of Tb(Ⅲ) at 490, 543, 584, and 621 nm. Tb-ddb has a high stability in water or common organic solvents. The sensitivity test shows a linear fitting equation of I 0 /I = 0.00443·C Glu + 0.93563 with LOD = 1.40 μM at C Glu = 0–500 μM. The detection performance of Tb-ddb is not affected by seven interferents of amino acids. High durability is supported by the stable emission intensities at 543 nm of blank Tb-ddb and Tb-ddb/Glu suspensions in five fluorescence quenching-recovery cycles. The returned C Glu close to the set C Glu and the recoveries around 100% demonstrate Tb-ddb sensing Glu in human urine and serum is reliable. The linear relationship between green value of the Tb-ddb strip and C Glu can realize the on-site Glu detection. Tb-ddb can be regarded as a promising fluorescence turn-off sensor to Glu with high sensitivity, selectivity and durability. A turn-off fluorescence sensor of Tb-ddb exhibits a quantitative fluorescence quenching to glutamic acid in human urine and serum. [Display omitted] • Tb-ddb shows a LOD of 1.40 μM in a linear range of 0–500 μM Glu, better than or compared to most MOF-based Glu sensors. • Tb-ddb shows high accuracy and the recovery around 100% for sensing Glu in human urine and serum. • Paper-based Tb-ddb shows a possbility for the on-site Glu detection with a linear equation of the green values vs C Glu. [ABSTRACT FROM AUTHOR]

MoS 2 and WS 2 are two promising candidates for photocatalytic hydrogen production, and pyrolysis is one of the conventional and useful methods for their preparations. However, systematic investigations about the influences of pyrolysis conditions on their photocatalytic hydrogen production performances are still unreported. Then in this paper, a series of pyrolysis products of ammonium tetrathiomolybdate (ATM) and ammonium tetrathiotungstate (ATT) were prepared by changing the pyrolysis temperature and time. Besides, detailed characterizations were conducted to find out the changes in composition, crystallinity, and morphology. Especially, to get optimal pyrolysis conditions for the preparation of high-performance MoS 2 and WS 2 , their photocatalytic hydrogen production activities were investigated. The results showed that although along with the changes in pyrolysis conditions, the overall changes in composition, crystallinity and morphology are similar for ATM and ATT products, there are significant differences in their performances. For the pyrolysis of ATM, the products obtained under lower temperatures exhibit relatively higher activity than those obtained under higher temperatures. The performance of sample ATM-400-1 (the pyrolysis product obtained under 400 °C 1 h) is the highest and those of two ATM-600 samples (obtained under 600 °C 1 h and 600 °C 2 h) are the lowest. On the contrary, for the pyrolysis of ATT, the higher-temperature products possess much higher performance than the lower-temperature ones. The activity of ATT-400-2 is the highest and those of two ATT-250 samples are the lowest. On the other hand, unconventional crystallized WS 3 was unexpectedly obtained through the pyrolysis of ATT at 300 °C for the first time. This work can offer useful information for the preparation of WS 2 and MoS 2 -based photocatalysts. The optimal conditions for preparation of MoS 2 and WS 2 by pyrolysis of ammonium tetrathiomolybdate (ATM) and ammonium tetrathiotungstate (ATT) were achieved and the reasons for performance difference of different products were elucidated. [Display omitted] • Pyrolysis products of ATM and ATT were systematically characterized. • Hydrogen production performances of pyrolysis products were detailed investigated. • Reasons for performance differences between ATM and ATT products were elucidated. • Crystalline WS 3 was achieved for the first time by the pyrolysis of ATT. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) have been widely used in filed of electrochemistry. Compared with traditional inorganic porous materials, the polyvalent pyridinecarboxylic acid ligands have many advantages which contains more active sites, flexible coordination mode, adjustable structure. Therefore, it becomes good choice for constructing MOFs materials with excellent performance. In this paper, a novel MOF was synthesized by pyridine polycarboxylic acid ligand and CoCl 2 ·6H 2 O using solvothermal method. The physicochemical properties were characterized by FT-IR, powder diffraction and thermogravimetry. Single crystal X-ray diffraction reveal that MOF-1 crystallizes in monoclinic system with P 2 1 / C space group. The central Co2+ ions have a dual core structure with 5 and 6 coordination, respectively. The carboxyl groups show two kinds of coordination modes μ 2 : η1: η1 and μ 2 : η1: η2, and the pyridine N atoms also coordinate to form a three-dimensional network structure. Electrochemical experiments show that MOF-1 has a lower overpotential (339.4 mV) and Tafel slope (65.3 mV·dec−1) with higher ECSA and better OER kinetics. A large number of exposed active sites indicate that the MOF has higher potential as catalyst for oxygen evolution reaction. [Display omitted] • A Co-MOFs based on pyridine polycarboxylic acid ligand were prepared by a simple hydrothermal method. • Electrochemical test show that the MOFs has a lower overpotential and Tafel slope with higher ECSA and better OER kinetics. • MOFs exhibit a porous three-dimensional network structure. [ABSTRACT FROM AUTHOR]

The oxygen evolution reaction is more challenging than the hydrogen evolution reaction in overall water splitting, not only because the four-electron reaction is more complex but also because the oxidizing environment of the anode reaction is more destructive to the electrode material. Generally, such destruction results in the formation of an oxide film that hinders the transition of electrons and subsequently decelerates the succeeding reaction. This paper proposes a transition layer for self-supporting electrodes (NiFe LDH@NiCoP/NF) in which NiCoP grows between the NF and NiFe LDH. The implementation of NiCoP as a transition layer, showcasing excellent antioxidation capability and conductivity, effectively reduced overpotentials and consequently enhanced the catalytic performance. Benefiting from this transition layer, in a 1.0 M KOH, the NiFe LDH@NiCoP/NF catalyst exhibited outstanding OER and HER performance, requiring only 281 and 102 mV, respectively, to achieve 100 and 10 mA cm−2, and also exhibited a cell voltage for overall water splitting of 1.56 V at 10 mA cm−2. The NiFe LDH@NCP/NF composite was successfully synthesized by employing hydrothermal, phosphorization, and electrodeposition techniques to introduce the NCP transition layer between NiFe LDH and the NF substrate. The excellent performance in both OER and HER endows the NiFe LDH@NCP/NF composite with significant potential in the field of overall water splitting. [Display omitted] • NiFe LDH@NCP/NF was obtained by introducing a needle-like NiCoP (NCP) between the amorphous NiFe LDH and the NF substrate. • The NCP, with its excellent antioxidation capability and conductivity, enhances the OER performance of the NiFe LDH@NCP/NF. • By optimizing the electrodeposition time of NiFe LDH, the electrochemical active surface area was maximized. • During the overall water splitting, the NiFe LDH@NCP/NF electrode attains a low voltage of 1.56 V at 10 mA cm−2. [ABSTRACT FROM AUTHOR]

The development of highly efficient and low-cost bifunctional electrocatalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is the key to the industrialization of large-scale hydrogen production, while the development of non-precious-metal catalysts that can be substituted for precious-metal materials is the current trend of research. In this paper, nickel foam (NF) self-supported CoFe layered bimetallic hydroxide (LDH)-CuCo 2 S 4 electrocatalysts were prepared using a simple hydrothermal and electrodeposition method. The prepared CuCo 2 S 4 @CoFe-LDH/NF catalysts showed good performance in alkaline water oxidation, proton reduction and overall water decomposition with an overpotential of 293 mV for the oxygen evolution reaction (OER) at a current density of 50 mA cm−2 and 63 mV for the hydrogen evolution reaction (HER) at a current density of 10 mA cm−2. When CuCo 2 S 4 @CoFe-LDH/NF was used as a bifunctional electrocatalyst for the decomposition of water, the voltage of the 10 mA cm−2 electrolyzer was only 1.54 V, and the stability of the electrolyzer reached 60 h, which was superior to other bifunctional catalysts. [Display omitted] • CoCu-LDH grows firmly on nickel foam by a hydrothermal method. • Vulcanization at room temperature makes the experimental conditions milder and simpler. • An electrodeposition method was used to grow nanosheets on nanowires. [ABSTRACT FROM AUTHOR]

Porous materials with high adsorption capacity can enhance the efficiency of water-based adsorption heat transformation systems. The composites salt in porous matrix (CSPM) are considered to be very promising materials. In this paper, the UIO-66-NH 2 and UIO-66-NO 2 metal-organic framework were used as the porous matrix to synthesize composites with CaCl 2 as the hygroscopic salt. The water adsorption and desorption performance of the composite materials were studied, and the cycle stability was investigated in a continuous adsorption-desorption experiment. As a result, the hydrophilic UIO-66 based composites exhibited higher water adsorption and heat storage capacity. CaCl 2 @UIO-66-NH 2 achieved a water adsorption capacity of 0.84 g/g at 60% relative humidity (RH) and an energy storage density of 1858 J/g. In addition, the hydrophilic UIO-66 based composites exhibited excellent cycle stability, with the quality decreasing by less than 5% after ten adsorption-desorption cycles. By introducing hydrophilic functional groups, the adsorption capacity, adsorption rate, and thermal storage capacity of CSPMs were improved. [Display omitted] • The hydrophilic functionalized UIO-66 based composites exhibit enhanced water absorption properties. • The hydrophilic functionalized samples have higher energy storage densitywith CaCl 2 @UIO-66-NH 2 reaching 1858J/g. • All samples exhibited good cycle stability and the water adsorption quantity decreased by less than 5% after 10 cycles. [ABSTRACT FROM AUTHOR]

The luminescent properties of main-group metal-organic frameworks (MOFs) can usually be modulated by organic ligands, and thus realizing temperature sensing over a wide range. Herein, a step-by-step decoration of hydroxyl groups on terephthalic acid (BDC) ligand was involved to regulate the excited-state intramolecular proton transfer (ESIPT) process of the ligands and thus the temperature sensing performance. Accordingly, the OH groups located on these ligands effectively regulate their luminescence sensing property with the absolute temperature sensing sensitivity following the order: DHBDC (0.62% K−1) > OHBDC (0.26% K−1) > BDC (no obvious linear relationship). Luminescent main-group MOFs with these ligands, namely MIL-53-Al-BDC/OHBDC/DHBDC and SNNU-301-Mg-DHBDC, were further selected to explore the temperature sensing performance. Thanks to the unique fluorescence characteristics of the DHBDC ligand, MIL-53-Al-DHBDC and SNNU-301-Mg-DHBDC both demonstrate excellent temperature sensing ability over a wide range (80–480 K) with the absolute temperature sensing sensitivity of 0.32% K−1 and 0.35% K−1, respectively. The compared luminescent spectra show that the stronger electron-donating ability of the substituents on the benzene ring can lead to the higher the electron cloud density in the MOF structure, and thus bring a higher temperature sensing sensitivity. This paper pays a new way for the exploration of practical wide-range MOF thermometers. [Display omitted] • Step-by-step regulation of ESIPT process by hydroxyl groups. • Main-group MOFs with ESIPT ligands. • MOFs with excellent wide-range temperature sensing performance. [ABSTRACT FROM AUTHOR]

Due to high stability, safety and energy density properties, solid-state lithium-ion is expected to be used for the next-generation batteries. Recently, new solid electrolyte materials with high-ion conductivity have been widely explored. In this paper, a novel solid electrolyte LiNaSrP 2 O 7 was successfully prepared by the conventional solid-state method and characterized by X-ray diffraction (XRD) analysis, electron microscopy and optical and impedance spectroscopy. XRD and Rietveld analysis show that the sample crystallizes in the orthorhombic structure with Pnma space group. The UV–Vis measurement, performed from 200 nm to 800 nm, show a direct optical band gap evaluated at 5.26 eV. Both impedance and modulus studies reveal the temperature-dependent non-Debye type relaxation conduction phenomenon. AC conductivity has been studied to understand the conduction mechanism. AC conductivity results show the role of quantum mechanical tunneling of charges in the conduction mechanism. Moreover, the electrical conductivity and modulus analysis findings revealed the activation energy obtained from suggests that the transport takes place through the ion hopping mechanism, dominated by the motion of the mixed Li+/Na+ ions in the structure of the investigated material. [Display omitted] • The compound crystallizes in the orthorhombic structure with Pnma space group. • Optical study proved that the indirect band gap is around 5.26 eV. • The electrical properties suggesting the semiconductor behavior. • The variation of M″ peak showed a thermally activated relaxation process. • The near value of activation energies obtained from the analysis of M″, dc-conductivity and hopping frequencies data confirms that the transport is through ion hopping mechanism, dominated by the motion of the mixed Li+/Na+ ions in the structure of the investigated materials. [ABSTRACT FROM AUTHOR]

In this paper, Short-time X-ray irradiation induced long afterglow and photostimulated luminescence from Sr 2 GeO 4 : Pr3+ has been observed. Under the X-ray irradiation, Sr 2 GeO 4 : Pr3+ can produce long afterglow and photostimulated visible luminescence mainly located at 490, 547 and 629 nm, which are attributed to 3P 0 →3H 4 , 3P 0 →3H 5 and 3P 0 →3H 6 of Pr3+, respectively. More important, even 5 s X-ray irradiation which was less than the X-ray damage from one CT scan, can induce 5400 s afterglow emission. Furthermore, due to its excellent photostimulated luminescence properties, the afterglow emission intensity of Sr 2 GeO 4 : Pr3+can be significantly improved under the radiation of 980 and 808 nm lasers and the emission intensities can still be maintained even after 12 testing cycles. The thermoluminescence results show that Pr3+ doping produces three different traps. Among these, the traps with 0.64 and 0.71 eV trap depth result in excellent X-ray long afterglow luminescence of Sr 2 GeO 4 : Pr3+. While the deep trap of 0.96 eV determines the photostimulated luminescence properties. These results indicate that Sr 2 GeO 4 :Pr3+ possesses excellent long afterglow and photostimulated luminescence under the X-ray irradiation in safety range, which thus can be regarded as in vivo light source to efficiently conduct photodynamic therapy in the future. Sr 2 GeO 4 :Pr3+ long afterglow material has been prepared, which has the characteristics of Short-time irradiation by X-ray induced long afterglow and photostimulated luminescence. The result showed that the afterglow emission peaks are mainly located at 490 nm, 547 nm and 629 nm, corresponding to the 3P 0 →3H j (j = 4, 5, 6) characteristic transitions of Pr3+, respectively. When the doping concentration of Pr3+ is 0.5 %, the sample possesses the best afterglow and the afterglow emission can still be observed after 5400 s. And the X-ray excitation can produce much better afterglow performance than 254 nm excitation. In addition, the sample also showed good afterglow performance under short-time (5 s) X-ray radiation. At the same time, the sample possesses strong PSL characteristics under the excitation of 980 nm and 808 nm lasers and still maintains strong PSL afterglow intensity after 12 cycles of measurements. Furthermore, the trap density under X-ray excitation is much higher than that under UV excitation, which thus produce much longer afterglow emission under the X-ray irradiation. These results indicate that Sr 2 GeO 4 :Pr3+ possesses excellent long afterglow and photostimulated luminescence under the X-ray irradiation in safety range, which thus can be regarded as in vivo light source to efficiently conduct photodynamic therapy in the future. [Display omitted] • X-ray induced long afterglow material Sr 2 GeO 4 :Pr3+ shows excellent photostimulated luminescence properties. • Sr 2 GeO 4 :Pr3+ showed good afterglow performance under short-time (5 s) X-ray radiation. • A model is presented to clarify the afterglow mechanisms of Sr 2 GeO 4 :Pr3+. [ABSTRACT FROM AUTHOR]

As an important next-generation photoelectric material, the controlled synthesis of two-dimensional molybdenum disulfide (2D MoS 2) with high uniformity is imperative. Traditional MoS 2 growth methods in the open space usually require a large amount of raw materials and have poor uniformity of growth results. In this paper, we report a space-confined method for uniformly growing large MoS 2 flakes on the SiO 2 /Si substrate. As the precursor film coated on the bottom substrate is restricted in a small confined space between the top and bottom substrates separated by a small spacer, it is efficiently utilized, achieving large MoS 2 flakes with good uniformity on the top substrate. By further tuning the content of NaCl catalyst in the precursor, single-layer or multi-layer MoS 2 flakes can be obtained in a controlled manner, and well characterized by Raman, XPS, PL and AFM. The uniform distribution of Mo-containing species and its high concentration in the confined space, contributing to the efficient growth of uniform large MoS 2 flakes. This research will provide guidance for rational synthesis of 2D MoS 2 flakes on dielectric substrates. A space-confined method is proposed to grow large MoS 2 flakes uniformly and efficiently on the SiO 2 /Si substrate. [Display omitted] • A space-confined method for growing large MoS 2 flakes uniformly and efficiently on the SiO 2 /Si substrate is proposed. • This method is featured with ultralow precursor consumption and high growth uniformity of MoS 2 flakes. • Monolayer or multilayer MoS 2 flakes can be obtained in a controlled manner by adjusting the content of NaCl catalyst. [ABSTRACT FROM AUTHOR]

Replacement of the Harber-Bosch process for urea production by electrochemical reduction is an attractive alternative that reduces chemical energy consumption, reduces environmental pollution and improves efficiency. Among them, the method of electrochemical coupling of N 2 and CO 2 to produce urea has been widely used, but the inertness of nitrogen and nitrogen bond and high dissociation energy make it difficult to activate N 2. Meanwhile, the method of synthesis of urea by NO 3 RR came into being. Nitrate in sewage is more abundant and convenient than nitrogen raw material, and more importantly, the dissociation energy of N O bond is much lower than that of N N. In this study, the transition metal embedded lithium COF catalyst was taken as an example, and the optimal electrocatalyst was selected through screening and synthesis energy barrier comparison to study the mechanism of urea synthesis. We studied the NRR and NO 3 RR paths, respectively, and found that the NRR synthesis of urea was optimal on the LiTaS-Pc VPPs catalyst, with a limiting potential value of −0.57V, and the NO 3 RR synthesis of urea was optimal on the LiVS-Pc VPPs catalyst, with a limiting potential value of −0.39V. It is found that NO 3 RR on the lithium catalyst is relatively better, and the required limit potential value is lower. In addition, the advantage of choosing lithium metal doping as catalyst in our study is that HER can be well inhibited, and the desorption of urea is easier than that of transition metal doping (taking molybdenum as an example). This study points out the direction for the electrocatalytic synthesis mechanism of urea, and provides a new idea for the selection of catalysts, paving the way for the future production of urea. This paper investigated the mechanism of urea synthesis using NRR and NO 3 RR on lithium-based COF series catalysts (LiTMS-Pc VPPs), respectively. Among them, the adsorption of reactive nitrogen, C–N coupling, and urea synthesis are mainly carried out on LiTMS-Pc. The process of generating CO via CO 2 RR on VPPs overflows onto the phthalocyanine structure and undergoes C–N coupling with nitrogen-containing intermediates to synthesize urea. Comparing and organizing the two methods of urea synthesis, NO 3 RR is relatively superior. In addition, a comparison was made between the synthesis of lithium-based catalysts and transition metal molybdenum catalysts, and it was found that the lithium-based catalyst improved urea removal. [Display omitted] • The synthesis of urea on a two-dimensional carbon-rich catalytic structure is studied using the cascade catalytic approach. • The main group metal lithium is embedded in the catalyst, and the synthesis of urea under the action of lithium-based and molybdenum-based catalysts is studied and compared. • Compare excellent urea synthesis using N 2 and NO 3 as different nitrogen sources. [ABSTRACT FROM AUTHOR]

Hydrogen energy is considered as powerful alternative to fossil energy owing to its virtues of high energy density, eco-friendliness and low cost. Metal-organic frameworks (MOFs) can be used as ideal precursors through carbonization used as electrocatalysts in energy storage and coversion fields, which will inherit the merits of ordered structures and large surface area. In this paper, Co-G@C centering on Cobalt as hydrogen evolution electrocatalyst synthesized by carbonizing CUST-515 decorated with glucose as carbon source. Co-G@C possess the overpotentials of 162 and 193 mV at the current density of 10 mA cm−2 in alkaline and acid solutions with long as 24 h stability. This good effect is attributed to the coupled effect of Co and carbon layers as well as the large and ordered pore structures induced by glucose and CUST-515 carbonization, which can accelerate the charge transfer. This work can come up with a reference for the synthesis of non-expensive metal electrocatalysts for water splitting applications. the electrocatalyst Co-G@C was synthesized by one-step high-temperature calcination by mixing glucose with A new MOF (CUST-515). Co-G@C exhibits excellent HER properties in alkaline and acidic solutions. [Display omitted] • A new MOF (CUST-515) was prepared by solvothermal method. • The electrocatalyst Co-G@C was synthesized by one-step high-temperature calcination. • Co-G@C exhibits satisfactory hydrogen production performance. • This research provides a reference to synthesize non-noble metal electrocatalysts. [ABSTRACT FROM AUTHOR]

In this paper, we conducted a study on the structural modulation and photocatalytic performance of single-phase hollow BiFeO 3 nanofibers (SPH–BFO NFs) photocatalysts, investigated the effect of heat treatment temperature on the structure of BFO NFs and the formation mechanism of a hollow structure. The SPH-BFO NFs consist of BiFeO 3 nanocrystals without other heterogeneous phases, with diameters of 400–600 ​nm and extraordinary flexibility, allowing easy separation of the catalyst from the solution. As a result, the SPH-BFO NFs possess outstanding photocatalytic performance and higher photocatalytic efficiency compared with other forms of BiFeO 3. In addition, the effects of different environments and water quality on RhB degradation were investigated. It was found that the vacancies (h+) and superoxide radicals (·O 2 −) as active substances were less environment-dependent, making the SPH-BFO NFs more resistant to environmental interference. The RhB degradation efficiency of BFO NFs was about 99% in 10 ​mg/L of RhB dye solution at pH ​= ​6. This work provides valuable insights into the application of SPH-BFO NFs in photocatalysis and the design of nanofiber photocatalysts. In this paper, SPH-BFO NFs with numerous photocatalytic active sites were prepared by electrostatic spinning technology combined with sol-gel method to achieve efficient degradation of Rhodamine B in wastewater. [Display omitted] • SPH-BFO NFs are prepared by the precursor sol-gel method in combination with the electrostatic spinning technique. • SPH-BFO NFs have superior photocatalytic properties and higher photocatalytic efficiency in wastewater. • SPH-BFO NFs can easy separation of the catalyst from the solution because of extraordinary flexibility. • SPH-BFO NFs have a strong ability to resist environmental interference. [ABSTRACT FROM AUTHOR]

High entropy oxides (HEOs) are characterized by a single-phase in which multiple cations are responsible for elevating the endothermicity and stability of the system. However, it is still difficult to predict the single-phase structure of high entropy oxides due to the complex composition. This paper considers the chemical-short range order and proposes a novel design method for a creative kind of A 32 Ti 8 Sn 8 Nb 4 Ta 4 Me 8 O 96 (A = Ba, Sr; Me = Fe, Ga) perovskite structure high entropy oxides (PHEOs) based on the cluster-plus-glue-atom model, and the photocatalytic performance of the synthesized samples was investigated. Results indicated that the PHEOs are successfully synthesized, and their compositions are not constrained by equimolar cations, hence expanding the composition into non-equimolar range. The as-prepared PHEOs exhibit good photodegradation ability of Cr (VI) contaminant. This article firstly proposes a new strategy for the design of PHEOs and gives a further exploration for the application of PHEOs in photocatalysts. This paper considers the chemical-short range order and proposes a design method for perovskite structured high entropy oxides based on cluster-plus-glue-atom model. The designed new kinds of perovskite structure high entropy oxides were further synthesized by solid state reaction method, and their optical properties and photocatalytic degradation efficiency of Cr (VI) to Cr (III) were investigated. This work opens up a new direction in the design of high entropy oxides with good photocatalytic performance. [Display omitted] • A new design method for perovskite structure HEOs was presented based on cluster-plus-glue-atom model. • The synthesized perovskite structure HEOs are not constrained by equimolar cations. • The cell parameters and properties of perovskite structure HEOs can be adjusted by the introduction of different elements. • Photocatalytic performance of perovskite structure HEOs was investigated. [ABSTRACT FROM AUTHOR]

Urease may rapidly hydrolyze urea, causing a significant amount of ammonia to be released and decreasing the efficacy of urea fertilizers. However, urease inhibitors (UIs) can inhibit the interaction between urease and urea so that ammonium nitrogen can be absorbed by crops for a long time. In this paper, we developed and fabricated two Cu-based coordination polymers (Cu-CPs) to function as UIs by combining two aromatic carboxylic acids and a bis-pyridine-bis-amide ligand, which demonstrate outstanding urease inhibitory efficacy. Cu-CP-1 exhibits a pronounced inhibitory effect on the inhibitory activity of jack bean urease while the semi-inhibitory concentration (IC 50) value was 0.74 ± 0.01 μM, whereas the IC 50 value of Cu-CP-2 was 4.77 ± 0.51 μM. Furthermore, inhibitory activity against urease, kinetic, molecular docking, and comparisons of the title Cu-CPs and other complex-based materials have been comprehensively investigated. More importantly, the oxygen atoms of μ 2 -OH and –COO play important roles in urease inhibition activity. The structure–function relationship were further discussed which indicates that Cu-CPs can be used as a kind of UIs. By using different O-donor second auxiliary ligands, we have designed and synthesized two Cu-based CPs to operate as urease inhibitors which show excellent urease inhibitory activity. [Display omitted] • The development of UIs has been a matter of great concern to researchers. • Two Cu-CPs have been synthesized by using diverse O-donor ligands. • The Cu-CPs are served as UIs and show excellent urease inhibitory activity. • Inhibitory activity, kinetic, molecular docking of the Cu-CPs have been studied. [ABSTRACT FROM AUTHOR]

BiFeO 3 has excellent potential as a narrow band gap semiconductor and piezoelectric material for photoelectrochemical decomposition of water (PEC) applications. However, because of its susceptibility to impurities and oxygen vacancy defects during preparation and its high complexation rate of photogenerated carriers, relevant applications are greatly limited. In this paper, BiFeO 3 /CdS heterojunction films were prepared on FTO conductive glass by a very simple and feasible sol-gel and chemical bath method to improve the efficiency of the photoelectrochemical decomposition of water. It was shown based on a series of PEC tests. The photocurrent density of the pure BiFeO 3 thin film photocathode reached −85 μA/cm2 after giving ultrasonic stress conditions. Furthermore, the BiFeO 3 /CdS heterojunction photocathode achieved a photocurrent density of about −230 μA/cm2 at 0 V vs. RHE under the synergistic effect of piezoelectric polarization and the built-in electric field built in the heterostructure. In summary, semiconductor modification approaches using the construction of suitable heterojunction structures can effectively promote the separation and transfer of carriers between interfaces. The use of piezoelectric polarization and the search for appropriate energy level-matched semiconductors to construct heterojunctions can synergistically improve the efficiency of piezoelectric photocatalysis. The composite of BiFeO 3 and CdS to form type II heterojunction effectively improves the photoelectrocatalytic performance of BiFeO 3 under piezoelectric effect. [Display omitted] • Both BiFeO 3 and CdS films are in the form of nanosheets and the fabrication process is simple and can be done in the laboratory. • Compared with the enhancement of piezoelectric effect under ultrasonic condition, the internal electric field formed by heterojunction can further increase the concentration of photogenerated carrier, thus improving its separation efficiency. [ABSTRACT FROM AUTHOR]

In this paper, first-principle calculations based on density-functional theory (DFT) and plane-wave pseudopotential basis for g-C 3 N 4 /ZnO composites were carried out using Quantum Espresso (QE) code. The g-C 3 N 4 /ZnO composite photocatalytic materials were prepared by solid-phase calcination and characterized by XRD, SEM, and FT-IR. Photocatalytic degradation experiments were carried out under LED light irradiation, using the dye rhodamine B (RhB) and the antibiotic tetracycline hydrochloride (TC) as simulated degradation targets. The degradation performance of the composites was tested using the commercially available pesticide glyphosate. The removal of total nitrogen (TN), total phosphorus (TP), and chemical oxygen demand (COD) from water samples was tested using real sewage livestock wastewater. The photocatalytic degradation mechanism of the composites was explored by free radical trapping experiments. Finally, the MTT cytotoxicity test demonstrated that the g-C 3 N 4 /ZnO composite photocatalytic materials are non-cytotoxic and are expected to be used in wastewater treatment. Photocatalytic degradation diagram. [Display omitted] • In this study, a combination of theoretical calculations and experiments was used to investigate the g-C 3 N 4 /ZnO composite photocatalytic materials. • RhB and TC were taken as simulated degradation targets to test the degradation performance of g-C 3 N 4 /ZnO composite photocatalytic materials, and then the photocatalytic degradation of the composites for real pesticides was tested using the pesticide glyphosate. • Real sewage livestock wastewater was used to test the removal of total nitrogen (TN), total phosphorus (TP), and chemical oxygen demand (COD) from water samples by the composites. • The material successfully passed the MTT cytotoxicity test, and it can be concluded from the above experiments that the material is expected to be put into the treatment of real sewage. [ABSTRACT FROM AUTHOR]

The irreplaceable silicone materials among the high-tech industry is dimethyldichlorosilane, a monomer whose by-products generated in the synthesis step can be recycled through disproportionation reactions. In this paper, the catalytic activities of NH 2 -MIL-53(Al)@γ-Al 2 O 3 with Brønsted acid active sites and AlCl 3 /NH 2 -MIL-53(Al)@γ-Al 2 O 3 core-shell catalysts with Lewis acid active sites were investigated and compared for the disproportionation to prepare dimethyldichlorosilane by means of the M06-2X/Def2-TZVP hybrid functional method. The results given for structure, energy, vibrational frequency, IRC values, bond order, ELF and LOL analysis were matched. The results showed that AlCl 3 /NH 2 -MIL-53(Al)@γ-Al 2 O 3 core-shell catalyst with Lewis acid was more active. Simulated synthesis and interatomic correlation parameters (bond length/nm and bong angle/o) of NH 2 -MIL-53(Al)@γ-Al 2 O 3 (Cat. ,active site No.1-3) and AlCl 3 /NH 2 -MIL-53(Al)@γ-Al 2 O 3 (Cat.&, Configuration a-d). [Display omitted] • Proposed four- and six-step disproportionation allows recycling of (CH 3) 3 SiCl and CH 3 SiCl 3. • Loading of AlCl 3 presents Lewis catalytic centers, which possess enhanced catalytic activity compared to Brønsted acid. • Optimization of MOFs-based catalysts with core-shell structure, NH 2 -MIL-53(Al)@γ-Al 2 O 3 and AlCl 3 /NH 2 -MIL-53(Al)@γ-Al 2 O 3. [ABSTRACT FROM AUTHOR]

It's still a challenge to design reasonably efficient catalyst using non-noble metal for the oxygen evolution reaction (OER). In this paper, we use a simple one-step electrodeposition method to load Ce and S co-doped NiFe amorphous alloys onto Cu(OH) 2 nanorod arrays. The excellent oxygen electrocatalytic performance of the catalyst NiFeCeS/Cu(OH) 2 /CuF is attributed to the electronic environments of the active sites of Ni and Fe regulated by heteroatomic sulfur and cerium, which promote the transfer of the oxygen precipitation intermediates to the higher valence states. Meanwhile, the highly conductive substrate accelerates the electron transfer efficiency of the catalyst material, and the loose nanostructure increases the specific surface area, exposing more active sites. NiFeCeS/Cu(OH) 2 /CuF shows outsanding electrocatalytic activity for oxygen evolution with a low overpotential of 227 mV at a current density of 10 mA cm−2 in alkaline medium. Moreover, the nanocomposite catalyst also exhibits rapid reaction kinetics and long-term stability and durability. In this work, an efficient oxygen precipitation catalyst is reported, which indicates that non-precious metal-based electrocatalysts have great potential for application in water electrolysis and provides a basis for the rational design and synthesis of nanorod array catalysts with unique structures. Using a simple one-step electrodeposition method to load Ce and S co-doped NiFe amorphous alloys onto Cu(OH) 2 nanorod arrays. NiFeCeS/Cu(OH) 2 /CuF shows outsanding electrocatalytic activity for oxygen evolution with a low overpotential of 227 mV at a current density of 10 mA cm−2 in alkaline medium. [Display omitted] • Co-doping of Ce and S improved the intrinsic activity of NiFe catalysts. • Cu(OH) 2 nanorods increase the number of active sites in catalysts. • The one-step co-deposition technique is simple, efficient and repeatable. [ABSTRACT FROM AUTHOR]

To search for more high-performance crystalline proton conducting materials and to accelerate the related research progress, in this paper, a one-dimensional coordination polymer (CP), [Co(BBOT) 2 (H 2 O) 3 ·2H 2 O] n (1) (H 2 BBOT = N-benzoyl-N′-(4-benzoxy)thiourea) was firstly prepared by solvent volatilization approach. Subsequently, the thermal, H 2 O and chemical stabilities of the CP were tested and its high structural stability was confirmed. Furthermore, in 1 , a stable solid three-dimensional framework can be constructed by intermolecular H-bonds and stacking interactions between phenyl units. Then, utilizing the AC impedance determination, the dependence of the proton conductivity of this CP on temperature and humidity in the water vapor environment was explored and the positive correlation was verified. Excitingly, the optimized proton conductivity of this compound under specific test conditions (100 °C/98 % relative humidity) can be as high as 10−4 S/cm, being in the forefront of similar crystalline solid materials. Finally, according to the value of activation energy and the characteristics of crystal structure, we speculate on the proton conduction mechanism. Proton conductivity of a CP under variable humidity and temperatures was explored. Its highest proton conductivity can attain up to 10−4 S/cm, and its proton-conduction mechanism was speculated. [Display omitted] • One carboxylate-based Co(II) coordination polymer was prepared. • Its structure was characterized by single-crystal X-ray diffraction. • Its water-assisted proton conduction was explored. • The proton-conducting mechanism was speculated. [ABSTRACT FROM AUTHOR]

By introducing functional groups into the isophthalate ligand to decorate the pore of the MOFs, gas adsorption and separation performance can be tunable. In this paper, two isostructural 2D Co-MOFs, [Co(5-MIA)(bpy)]·H 2 O (1) and [Co(5-EIA)(bpy)]·H 2 O (2) (5-H 2 MIA = 5-methoxyl-isophthalic acid; 5-H 2 EIA = 5-ethyoxyl-isophthalic acid; bpy = 4,4′-bipyridine), with different functionalized pore surfaces and channel sizes were designed and constructed. The structures and performance of the two Co-MOFs were analyzed by SCXRD, PXRD, IR, TGA, and gas sorption (CO 2 , C 2 H 2 , CH 4 , CO, and N 2). Attributed to the methoxyl of isophthalate skeleton, 1a (activated 1) shows enhanced CO 2 uptake over other gases. In spite of decreased pore sizes (3.49 Å) compared with 2a (4.38 Å), the CO 2 uptake of 1a (43.41 cm3 g−1) is larger than that of 2a (22.39 cm3 g−1) at 298 K and 100 kPa. Compound 1 incorporates methoxyl groups into the narrow channel, and exhibits the cooperative effect of CO 2 -preferential due to adsorbent-adsorbate coactions and size sieving. GCMC simulation has been used to explore the adsorption coactions of CO 2 and 1 , and the results confirmed that the methoxyl groups in the channel are the main binding sites of CO 2. At ambient temperature and 100 kPa, the IAST selectivities of CO 2 /C 2 H 2 (1:1), CO 2 /CH 4 (1:1), C 2 H 2 /CH 4 (1:1), CO 2 /CO (1:2) and CO 2 /N 2 (15:85) on 1a were 2.6, 39.3, 13.3, 282 and 1433, respectively. The easy activation and regeneration, excellent thermal and humidity stability, and good reusability, make 1 a hopeful adsorbent for adsorption and separation of CO 2. By introducing functional groups into the isophthalate ligand to decorate the pore of the MOFs, gas adsorption and separation performance can be tunable. Two isostructural 2D Co-MOFs with different functionalized pore surfaces and channel sizes were constructed and show different C 2 H 2 /CH 4 and C 2 H 2 /CO 2 gas separation properties. [Display omitted] • Title compound represent the first example of 3D MOF based on 5-H 2 MIA and bpy. • 1a (activated 1) shows enhanced CO 2 uptake over C 2 H 2 , CH 4 , CO and N 2. • 1a shows an excellent reuse performance. [ABSTRACT FROM AUTHOR]