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Low mass-transfer efficiency and reaction-driving force make it difficult to realize thorough purification in traditional low-concentration pollutant treatments. Herein, we propose an "adsorption/catalysis in situ" perylene based bifunctional micelle for efficient, accurate and rapid adsorption and catalytic degradation of low-concentration bisphenol A (BPA). They show super-fast (within 10 s), high capacity (448 mg g

Capturing radioactive iodomethane and its vapors is a major challenge due to its low adsorption capacity. Herein, we have developed for the first time a pyridine-entrapped elastic crosslinked polysulfate gel (pyridine/TPC-cPS) as an efficient absorbent for iodomethane capture. Each pyridine-encased TPC-cPS network cell acts as a mini-reactor for salt formation between pyridine and iodomethane. The yield reaches up to 96.65 % and traps saturated iodomethane vapor of 1.573 g g

The catalytic room temperature oxidation of formaldehyde (HCHO) is widely considered as a viable method for the abatement of indoor toxic HCHO pollution. Herein, Pt/MnO2 nanoflowers anchored to boron nitride aerogels (Pt/MnO2 -BN) were fabricated for the catalytic room temperature oxidation of HCHO. The three-dimensional Pt/MnO2 -BN aerogels demonstrated superior catalytic activity as a result of the improved diffusion of the reactant molecules within the porous structure. Furthermore, the porous aerogels displayed excellent HCHO adsorption capacities, which promote a rapid HCHO gas-phase concentration reduction and a subsequent complete oxidation of the adsorbed HCHO. The combined adsorption and oxidation properties of the Pt/MnO2 -BN aerogels enhance the oxidative removal of HCHO. The optimized Pt/MnO2 -BN demonstrated excellent catalytic activity toward HCHO (200 ppm) at room temperature, achieving a 96 % formaldehyde conversion after 50 min.

Visible-light-responsive hierarchical Co9 S8 /ZnIn2 S4 tubular heterostructures are fabricated by growing 2D ZnIn2 S4 nanosheets on 1D hollow Co9 S8 nanotubes. This design combines two photoresponsive sulfide semiconductors in a stable heterojunction with a hierarchical hollow tubular structure, improving visible-light absorption, yielding a large surface area, exposing sufficient catalytically active sites, and promoting the separation and migration of photogenerated charges. The hierarchical nanotubes exhibit excellent photocatalytic H2 evolution and CrVI reduction efficiency. Under visible-light illumination, the optimized Co9 S8 /ZnIn2 S4 heterostructure provides a remarkable H2 generation rate of 9039 μmol h-1 g-1 without the use of any co-catalysts and CrVI is completely reduced in 45 min. The Co9 S8 /ZnIn2 S4 heterostructure is stable after multiple photocatalytic cycles.

BiOBr containing surface oxygen vacancies (OVs) was prepared by a simple solvothermal method and combined with graphitic carbon nitride (g-C3 N4 ) to construct a heterojunction for photocatalytic oxidation of nitric oxide (NO) and reduction of carbon dioxide (CO2 ). The formation of the heterojunction enhanced the transfer and separation efficiency of photogenerated carriers. Furthermore, the surface OVs sufficiently exposed catalytically active sites, and enabled capture of photoexcited electrons at the surface of the catalyst. Internal recombination of photogenerated charges was also limited, which contributed to generation of more active oxygen for NO oxidation. Heterojunction and OVs worked together to form a spatial conductive network framework, which achieved 63 % NO removal, 96 % selectivity for carbonaceous products (that is, CO and CH4 ). The stability of the catalyst was confirmed by cycling experiments and X-ray diffraction and transmission electron microscopy after NO removal.

Precious-metal catalysts (e.g., Au, Rh, Ag, Ru, Pt, and Pd) supported on transition-metal oxides (e.g., Al2 O3 , Fe2 O3 , CeO2 , ZrO2 , Co3 O4 , MnO2 , TiO2 , and NiO) can effectively oxidize volatile organic compounds. In this study, porous platinum-supported zirconia materials have been prepared by a "surface-casting" method. The synthesized catalysts present an ordered nanotube structure and exhibited excellent performance toward the catalytic oxidation of formaldehyde. A facile method, utilizing a boiling water bath, was used to fabricate graphene aerogel (GA), and the macroscopic 3D Pt/ZrO2 -GA was modified by introducing an adjustable MOF coating by a surface step-by-step method. The unblocked mesoporous structure of the graphene aerogel facilitates the ingress and egress of reactants and product molecules. The selected 7 wt.% Pt/ZrO2 -GA-MOF-5 composite demonstrated excellent performance for HCHO adsorption. Additionally, this catalyst achieved around 90 % conversion when subjected to a reaction temperature of 70 °C (T90 % =70 °C). The Pt/ZrO2 -GA-MOF-5 composite induces a catalytic cycle, increasing the conversion by simultaneously adsorbing and oxidizing HCHO. This work provides a simple approach to increasing reactant concentration on the catalyst to increase the rate of reaction.

Toxic gases that are colorless and odorless, such as CO, are a major environmental concern and require early detection to prevent serious toxicological effects. In this study, a unique system (Pt/HMSs-BRC) was fabricated by combining a catalyst (Pt/hollow mesoporous silica spheres, Pt/HMSs) with a silica gel containing an adsorbed chromogenic probe (binuclear rhodium complex, BRC). The process is a simple method to prepare well-dispersed and uniform Pt nanoparticles. The Pt/HMSs-BRC materials demonstrated early CO detection and excellent catalytic performance for CO oxidation. The probe exhibited remarkable color modulation from gray-violet to light-yellow when exposed to CO concentration levels above 50 ppm, and the color of the chromogenic probe was fully recoverable. By a kinetics-assisted discrimination method and DFT calculations, it was found that the corner Pt sites are the dominant active sites for CO oxidation.

Porous carbon (PC) materials with high surface area can separate electron-hole pairs and adsorb organic pollutants more effectively. A series of nanocomposites were prepared by anchoring black TiO2 nanoparticles (BTN) onto PC through a calcination process. Chemical and structural features of samples were examined by X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, powder X-ray diffraction (P-XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses. The resulting adsorption-photocatalysis synergistic effect led to a dramatically improved photocurrent for BTN@PCs, thus indicating the high photocatalytic performance toward water-soluble organic species. For instance, the degradation of tetracycline under visible light reached 90 %, which is higher than that for activated carbon doped onto BTN (57 %) without any additional agents. Moreover, the degradation of other antibiotics (such as oxytetracycline and ciprofloxacin) and methylene blue were also studied, thus showing that this system has the potential to be used for water treatment.

Catalytic performance is heavily dependent on how the structures of nanomaterials are designed. Co3 O4 -CeO2 composite nanotubes with open ends and mesoporous structures were fabricated through a facile and environmentally friendly reaction. The mesoporous Co3 O4 nanotubes were synthesized by the calcination of cobalt-aspartic acid (Co-Asp) nanowires and coated with a CeO2 shell. The composite nanotubes were characterized by SEM, TEM, XRD, and X-ray photoelectron spectroscopy. The composite materials comprise a combination of Co3 O4 nanotubes and CeO2 nanoparticles with a hollow and mesoporous bimetallic oxide structure. The large BET surface area led to a higher degree of accessible active sites compared with other Co3 O4 -CeO2 composite nanomaterials with other structures. The resulting Co3 O4 -CeO2 -26.3 wt % composite nanotubes, with a CeO2 content of approximately 26.3 wt %, achieved 100 % CO conversion at 145 °C. Additionally, the synergistic effect between the two metal oxides comprising the Co3 O4 -CeO2 composite nanotubes was demonstrated by the enhanced catalytic activity compared with pure Co3 O4 nanotubes and CeO2 nanoparticles.

Black phosphorus (BP), a star-shaped two-dimensional material, has attracted considerable attention owing to its unique chemical and physical properties. BP shows great potential in photocatalysis area because of its excellent optical properties; however, its applications in this field have been limited to date. Now, a Z-scheme heterojunction of 2D/2D BP/monolayer Bi2 WO6 (MBWO) is fabricated by a simple and effective method. The BP/MBWO heterojunction exhibits enhanced photocatalytic performance in photocatalytic water splitting to produce H2 and NO removal to purify air; the highest H2 evolution rate of BP/MBWO is 21042 μmol g-1 , is 9.15 times that of pristine MBWO and the NO removal ratio was as high as 67 %. A Z-scheme photocatalytic mechanism is proposed based on monitoring of . O2 - , . OH, NO2 , and NO3 - species in the reaction. This work broadens applications of BP and highlights its promise in the treatment of environmental pollution and renewable energy issues.

Polymeric materials have been widely used in the fabrication of data-storage devices, owing to their unique advantages and defined conduction mechanisms. To date, the most-functional polymers that have been reported for memory devices were synthesized through random copolymerization, whilst there have been no reports regarding the memory effect of block polymers. Herein, we synthesized a random copolymer (PMCz8 -co-PMBNa2 ) and its corresponding block copolymer (PMCz8 -b-PMBNa2 ) to study the effect of the method of polymerization on the memory properties of the corresponding devices. Interestingly, both devices (ITO/PMCz8 -co-PMBNa2 /Al and ITO/PMCz8 -b-PMBNa2 /Al) exhibited ternary memory performance, with threshold voltages of -1.7 V/-3.3 V and -2.7 V/-3.8 V, respectively. However, based on comprehensive measurements, the memory properties of PMCz8 -co-PMBNa2 and PMCz8 -b-PMBNa2 were found to be owing to the operation of different conduction mechanisms, which resulted from different molecular stacking in the film state. Therefore, we expect that this work will be helpful for improving our understanding of the conduction mechanisms in polymer-based data-storage devices.

The cathode material properties of the microbial fuel cell (MFC) have a quite important effect on their power generation capacity. Excellent oxygen reduction reaction (ORR) performance is the key to obtaining the remarkable capability of MFC. In this study, a series of catalysts are successfully prepared by a simple step-by-step hydrothermal, in situ growth, solution polymerization, and pyrolysis procedure. Here, the NiCo nanoparticles loading on nitrogen/carbon dual-doped matrix annealing at 800 °C (NiCo@DNC-800) under Ar shows good ORR activity with a maximum power density of 2325.60 ± 41.96 mW m

The precious metals (Au and Pt) loaded in mesoporous substrate (carbon and silicon) are popular materials for catalytic CO oxidation. However, the method of preparation of noble metals and the metal particle size of deposition in pore channels of mesoporous materials are serious issues for environmental applications. Herein, Au/HPCN porous catalyst, which is both durability and uniform, is synthesized by facile in-situ reduction route for continuous CO oxidation. In our approach, hollow porous carbon nanospheres (HPCN) was selected as the substrate due to its thermal stability, well-defined nanostructure and large surface area. Au nanoclusters (NCs) was loaded in the pore channels of HPCN because its stability and catalytic performance. The as-synthesized nanocomposite possess uniform size and highly porous structure. Moreover, it is worth noting that the CO oxidation not only occurred during the reduction of Au3+ ions but also catalyzed by the as-prepared Au/HPCN. Due to the thermostability, this catalyst could possibly apply to deal with CO pollution in engine exhaust and atmospheric.

Recently, surface engineering of the indium tin oxide (ITO) electrode of sandwich-like organic electric memory devices was found to effectively improve their memory performances. However, there are few methods to modify the ITO substrates. In this paper, we have successfully prepared alkyltrichlorosilane self-assembled monolayers (SAMs) on ITO substrates, and resistive random access memory devices are fabricated on these surfaces. Compared to the unmodified ITO substrates, organic molecules (i.e., 2-((4-butylphenyl)amino)-4-((4-butylphenyl)iminio)-3-oxocyclobut-1-en-1-olate, SA-Bu) grown on these SAM-modified ITO substrates have rougher surface morphologies but a smaller mosaicity. The organic layer on the SAM-modified ITO further aged to eliminate the crystalline phase diversity. In consequence, the ternary memory yields are effectively improved to approximately 40-47 %. Our results suggest that the insertion of alkyltrichlorosilane self-assembled monolayers could be an efficient method to improve the performance of organic memory devices.

Small-molecule-based multilevel memory devices have attracted increasing attention because of their advantages, such as super-high storage density, fast reading speed, light weight, low energy consumption, and shock resistance. However, the fabrication of small-molecule-based devices always requires expensive vacuum-deposition techniques or high temperatures for spin-coating. Herein, through rational tailoring of a previous molecule, DPCNCANA (4,4'-(6,6'-bis(2-octyl-1,3-dioxo-2,3-dihydro-1H-benzo[de]isoquinolin-6-yl)-9H,9'H-[3,3'-bicarbazole]-9,9'-diyl)dibenzonitrile), a novel bat-shaped A-D-A-type (A-D-A=acceptor-donor-acceptor) symmetric framework has been successfully synthesized and can be dissolved in common solvents at room temperature. Additionally, it has a low-energy bandgap and dense intramolecular stacking in the film state. The solution-processed memory devices exhibited high-performance nonvolatile multilevel data-storage properties with low switching threshold voltages of about -1.3 and -2.7 V, which is beneficial for low power consumption. Our result should prompt the study of highly efficient solution-processed multilevel memory devices in the field of organic electronics.

Herein, two molecules based on urea and thiourea, which differ by only a single atom, were designed, successfully synthesized, and fabricated into resistive random-access memory devices (RRAM). The urea-based molecule showed binary write-once-read-many (WORM) storage behavior, whereas the thiourea-based molecule demonstrated ternary storage behavior. Atomic-force microscopy (AFM) and X-ray diffraction (XRD) patterns show that both molecules have smooth morphology and ordered layer-by-layer lamellar packing, which is beneficial for charge transportation and, consequently, device performance. Additionally, the optical and electrochemical properties indicate that the thiourea-based molecule has a lower bandgap and may be polarized by trapped charges, thus the formation of a continuous conductive channel and electric switching occurs at lower bias voltage, which results in ternary WORM behavior. This study, together with our previous work on single-atom substitution, may be useful to tune and improve device performance in the future design of organic memory.

A cooperative photoelectrical strategy is proposed for effectively modulating the performance of a multilevel data-storage device. By taking advantage of organic photoelectronic molecules as storage media, the fabricated device exhibited enhanced working parameters under the action of both optical and electrical inputs. In cooperation with UV light, the operating voltages of the memory device were decreased, which was beneficial for low energy consumption. Moreover, the ON/OFF current ratio was more tunable and facilitated high-resolution multilevel storage. Compared with previous methods that focused on tuning the storage media, this study provides an easy approach for optimizing organic devices through multiple physical channels. More importantly, this method holds promise for integrating multiple functionalities into high-density data-storage devices.

Flexible memory devices have continued to attract more attention due to the increasing requirement for miniaturization, flexibility, and portability for further electronic applications. However, all reported flexible memory devices have binary memory characteristics, which cannot meet the demand of ever-growing information explosion. Organic resistive switching random access memory (RRAM) has plenty of advantages such as simple structure, facile processing, low power consumption, high packaging density, as well as the ability to store multiple states per bit (multilevel). In this study, we report a small molecule-based flexible ternary memory device for the first time. The flexible device maintains its ternary memory behavior under different bending conditions and within 500 bending cycles. The length of the alkyl chains in the molecular backbone play a significant role in molecular stacking, thus guaranteeing satisfactory memory and mechanical properties.

Nanocage-shaped Co3- x Zrx O4 solid-solution supports and the corresponding platinum loaded nanocomposites, yPt/Co3- x Zrx O4 (x =0.27, 0.50, 0.69; y = 0.5, 1.0, 2.0 wt.%), are successfully fabricated via a Cu2 O nanocube hard template method and a glycol reduction method, respectively. The hollow nanocage structures obviously improve surface areas; moreover, the Zr doping forms the Co3- x Zrx O4 solid-solution supports, and the corresponding yPt/Co3- x Zrx O4 catalysts promote the enhancement of catalytic performance. Catalytic activity toward toluene combustion is enhanced for the 2.0 wt% Pt/Co2.73 Zr0.27 O4 catalyst. The catalysts are characterized using multiple techniques. Pt nanoparticles are uniformly dispersed across the Co2.73 Zr0.27 O4 nanocage surface. The 2.0 wt% Pt/Co2.73 Zr0.27 O4 catalyst exhibits the highest catalytic activity among all the samples and demonstrates good stability, with 90% toluene conversion obtained at a temperature of 165 °C. The same catalyst accomplishes full toluene oxidation at 180 °C, at a weight hourly space velocity of 36 000 mL h-1 g-1 . The apparent activation energy (Ea ) over the yPt/Co2.73 Zr0.27 O4 samples are significantly lower than those over the Co3- x Zrx O4 supports, with the 2.0 wt% Pt/Co2.73 Zr0.27 O4 catalyst exhibiting the lowest Ea value. These findings demonstrate the potential of the 2.0 wt% Pt/Co2.73 Zr0.27 O4 catalyst as a promising catalyst toward atmospheric toluene removal.

Lack of clean water is a major global challenge. Membrane separation technology is an ideal choice for the treatment of industrial, domestic sewage owing to its low energy consumption and cost. However, membranes are highly susceptible to contamination, particularly during wastewater treatment, which has limited their practical applications in this field. Similarly, the flux of the membrane decreases with prolonged use due to its reduced interlayer spacing. Preparation of membranes with anticontamination properties and stable flux is the key to addressing this problem. In this study, a 2D heterostructure membrane with visible-light-driven self-cleaning performance is prepared via a self-assembly process. Notably, the addition of palygorskite increases the interlayer spacing of the graphene and heterojunction structures, which increases the flux of the membrane and avoids a decrease of the interlayer spacing of the membrane under pressure. The presence of a heterojunction with visible light catalytic properties effectively avoids membrane fouling and avoids a sharp decrease of the permeation flux. Importantly, the prepared 2D membrane has excellent separation performance for oil-water emulsions with both high flux and efficiency. These features suggest great potential for the prepared 2D membrane in wastewater treatment applications.

Efficient drug loading and selectivity in drug delivery are two key features of a good drug-carrier design. Here we report on such a drug carrier formed by using hollow mesoporous silica nanoparticles (HMS NPs) as the core and specifically designed multifunctional amphiphilic agents as the encapsulating shell. These nanocarriers combine the advantages of the HMS NP core (favorable physical and structural properties) and the versatility of an organic-based shell (e.g., specificity in chemical properties and modifiability). Moreover, both the properties of the core and the shell can be independently varied. The varied core and shell could then be integrated into a single device (drug carrier) to provide efficient and specific drug delivery. In vitro and in vivo data suggests that these drug nanocarriers are biocompatible and are able to deliver hydrophobic drugs selectively to target tumor cells. After the break of the pH-labile linkages in the shell, the drug payload can be released and the tumor cells are killed.

Organic small-molecule-based devices with multilevel electroresistive memory behaviors have attracted more and more attentions due to their super-high data-storage density. However, up to now, only ternary memory molecules have been reported, and ternary storage devices may not be compatible with the binary computing systems perfectly. In this work, a donor–acceptor structured molecule containing three electron acceptors is rationally designed and the field-induced charge-transfer processes can occur from the donors. Organic quaternary memory devices based on this molecule are successfully demonstrated for the first time. The switching threshold voltages of the memory device are –2.04, –2.73, and –3.96 V, and the current ratio of the “0,” “1,” “2,” and “3” states is 1:101.78:103.47:105.36, which indicate a low possibility of read and write errors. The results represent a further step in organic high-density data-storage devices and will inspire the further study in this field.

A polymer containing aldehyde active groups (PVB) was synthesized by atom transfer radical polymerization (ATRP), acting as a polymer precursor to graft a functional moiety via nucleophilic addition reaction. DHI (2-(1,5-dimethyl-hexyl)-6-hydrazino-benzo[de]isoquinoline-1,3-dione) and NPH (nitrophenyl hydrazine) groups, which contain naphthalimides that act as narrow traps and nitro groups that act as deep traps, were anchored onto the PVB at different ratios. A series of graft polymers were obtained and named PVB-DHI, PVB-DHI4 -NPH, PVB-DHI-NPH4 , and PVB-NPH. The chemical composition of the polymers was analyzed by (1) H-NMR spectroscopy and X-ray photoelectron spectroscopy (XPS). Memory devices were prepared from the polymers, and I-V characteristics were measured to determine the performance. By adjusting the ratio of different electron acceptors (DHI and NPH) to 4:1, ternary memory behavior was achieved. The relationship between memory behavior of PVB-DHIx NPHy and acceptor groups as well as their conduction mechanism were studied in detail.

Water pollution caused by chemical reagent leaking, industrial wastewater discharging, and crude oil spills has raised global concerns on environmental sustainability, calling for high-performance absorbent materials for effective treatments. However, low-cost materials capable of effectively separating oils and organic solvents from water with a high adsorption capacity and good recyclability are rare on the market. Here, a cost-effective method is reported to fabricate high-performance graphene modified absorbents through the facile thermal reduction of graphene oxide on the skeletons of melamine foam. By integrating the high porosity, superior elasticity, and mechanical stability of raw sponge with the chemical stability and hydrophobicity of graphene sheets, the as-fabricated graphene foam not only possesses a rough and superhydrophobic surface, but also exhibits an excellent adsorption performance and extraordinary recyclability for various oils and organic solvents. It is worth mentioning that the superhydrophobic surface also endows the graphene foam with an excellent efficiency for oil/water separation. More importantly, the cost-effective fabrication method without involving expensive raw materials and sophisticated equipment permits a scale-up of the graphene foam for pollution disposal. All these features make the graphene foam an ideal candidate for removal and collection of oils and organic solvents from water.

For the organic memory device with vertically arranged electrodes, controlling the film-packing to achieve highly oriented crystallite arrangement is critical but challenging for obtaining the satisfied performance. Here, the effect of backbone planarity on the crystallite orientation is studied. Two diketopyrrolopyrrole-based small molecules (NI2PDPP and NI2FDPP) are synthesized with increasing planarity by furan substitution for phenyl rings. Upon thin-film analysis by atomic force microscopy, X-ray diffraction, and grazing-incidence small-angle X-ray scattering, the orientations of these crystallites are demonstrated to be well controlled through tailoring molecular planarity. The highly planar NI2FDPP in film prefers out-of-plane crystallite orientation with respect to the substrate normal while the nonplanar NI2PDPP displays less ordered packing with a broad orientation distribution relative to the substrate. As a result, NI2FDPP-based memory device exhibits superior multilevel performance. More importantly, the oriented crystallite arrangement favors uniformity in NI2FDPP thin film, thus, the device displays higher reproducibility of memory effects. This study provides an effective synthetic strategy for designing multilevel memory materials with favorable crystallite orientation.

In this study, two structural isomers α-PBT and β-PBT, which only differ in the phenyl substituent position on the quinoline chromophore, have been designed and successfully synthesized. The influences of substituent position on the film morphology and the storage performance of the devices were investigated. Both molecules employed in the memory devices exhibited same nonvolatile binary (write-once-read-many-times; WORM) characteristics, but the switch threshold voltage (Vth) of the β-PBT-based device was clearly lower than that of the α-PBT-based device. Simulation results demonstrate that the variation of the phenyl substituent position led to different intermolecular stacking styles and thus to varied grain sizes for each film morphology. This work illustrates that altering the phenyl substituent position on the molecular backbone could improve the quality of the film morphology and reduce power consumption, which is good for the rational design of future advanced organic memory devices (OMDs).

One of the most pervasive environmental issues is water contaminated with oil or organic solvents; this global challenge calls for emerging materials that could effectively separate oil or organic solvents from water. Here, such a material is presented by integrating 3D porous graphene foam (GF) with a smart pH-responsive surface, showing switchable superoleophilic and superoleophobic properties in response to the medium pH. The key chemistry applied in this study is to modify the 3D porous GF with an amphiphilic copolymer containing a block of poly(2-vinylpyridine) and polyhexadecyl acrylate (P2VP-b-PHA), resulting in a smart GF (ss-GF) with an either superoleophilic or superoleophobic surface at different medium pH. The as-designed ss-GF can effectively absorb oil or organic solvents from the aqueous media by using its superoleophilic surface at pH of 7.0, and it can also completely release the adsorbates when the pH is switched to 3.0 (and the surface of ss-GF is therefore shifted to superoleophobic); with a continuous operation of many cycles (e.g., >10). Furthermore, the as-designed ss-GF shows superior absorption capacity for oil and organic solvent, with a high capacity of ≈196 times of the weight relative to that of the pristine ss-GF. The present work suggests encouraging applications of the ss-GF to water–oil and water–organic solvent separation.

ZIF-67-derived 3D hollow mesoporous crystalline Co3 O4 wrapped by 2D graphitic carbon nitride (g-C3 N4 ) nanosheets are prepared by low temperature annealing, and are used for the photocatalytic oxidation of nitric oxide (NO) at a concentration of 600 ppb. The p-n heterojunction between Co3 O4 and g-C3 N4 forms a spatial conductive network frame and results in a broad visible light response range. The hollow mesoporous structure of Co3 O4 contributes to the circulation and adsorption of NO, and the large specific surface area exposes abundant active sites for the reaction of active species. A maximum NO degradation efficiency of 57% is achieved by adjusting the mass of the Co3 O4 precursor. Cycling tests and X-ray diffraction indicate the high stability and recyclability of the composite, making it promising in environmental purification applications.

A cationic surfactant-assisted hydrothermal route is developed for the facile synthesis of graphene-like MoS2/graphene (GL-MoS2/G) composites based on the hydrothermal reduction of Na2MoO4 and graphene oxide sheets with L-cysteine in the presence of cetyltrimethylammonium bromide (CTAB), following by annealling in N2 atmosphere. The GL-MoS2/G composites are characterized by X-ray diffraction, electron microscopy, high-resolution transmission electron microscopy, and Raman spectroscopy. The effects of CTAB concentration on the microstructures and electrochemical performances of the composites for reversible Li+ storage are investigated. It is found that the layer number of MoS2 sheets decreases with increasing CTAB concentration. The GL-MoS2 sheets in the composites are few-layer in the case of 0.01∼0.03 mol L−1 CTAB of hydrothermal solution and single-layer in the case of 0.05 mol L−1 CTAB. The GL-MoS2/G composites prepared with 0.01–0.02 mol·L−1 of CTAB solution exhibit a higher reversible capacity of 940–1020 mAh g−1, a greater cycle stability, and a higher rate capability than other samples. The exceptional electrochemical performance of GL-MoS2/G composites for reversible Li+ storage could be attributed to an effective integration of GL-MoS2 sheets and graphene that maximizes the synergistic interaction between them.

Multifunctional theranostic systems with good biocompatibility, strong clinical imaging capability, and target specificity are the desired features of future medicine. Here, the design of a theranostic nanocomposite capable of simultaneous targeting and imaging of the cancer cells is presented. It releases its drug payload by a controlled release mechanism. The nanocomposite contains luminescent gold nanocluster (L-AuNC) photostable and biocompatible diagnostic probes conjugated to a folic acid (FA)-modified pH-responsive amphiphilic polymeric system for controlled drug release. The nanocomposite uses a core-satellite structure to encapsulate hydrophobic drugs and releases the drug payload in mildly acidic endosomal/lysosomal compartments by the action of the pH-labile linkages in the polymer. In vivo studies show the selective accumulation of the FA-conjugated nanocomposite in tumor tissues by folate-receptor-mediated endocytosis. These findings demonstrate the potential of the nanocomposite as a nontoxic, folate-targeting, pH-responsive drug carrier that is useful for the early detection and therapy of folate-overexpressing cancerous cells.

Nitrogen dioxide (NO2 ) emission has severe impact on human health and the ecological environment and effective monitoring of NO2 requires the detection limit (limit of detection) of several parts-per-billion (ppb). All organic semiconductor-based NO2 sensors fail to reach such a level. In this work, using an ion-in-conjugation inspired-polymer (poly(3,3'-diaminobenzidine-squarine, noted as PDBS) as the sensory material, NO2 can be detected as low as 1 ppb, which is the lowest among all reported organic NO2 sensors. In addition, the sensor has high sensitivity, good reversibility, and long-time stability with a period longer than 120 d. Theoretical calculations reveal that PDBS offers unreacted amine and zwitterionic groups, which can offer both the H-bonding and ion-dipole interaction to NO2 . The moderate binding energies (≈0.6 eV) offer high sensitivity, selectivity as well as good reversibility. The results demonstrate that the ion-in-conjugation can be employed to greatly improve sensitivity and selectivity in organic gas sensors by inducing both H-bonding and ion-dipole attraction.

Noble metals (Au, Pt, and Ru) loaded into carbon supports show excellent performance for CO oxidation. Herein, a tunable metal-organic framework (MOF) coating is applied to a macroscopic 3D Ru/graphene aerogel (Ru/GA) composite, using a facial step-by-step method. The open macroporous structure of the Ru/GA provides pathways for the access and diffusion of reactant and product molecules. The resulting HK (HKUST-1)-containing MOF composite exhibits good performance for CO adsorption. It can simultaneously adsorb and oxidize CO, which improves the reaction rate. In this work, the catalytic efficiency of the resulting catalyst is higher than that (≈48.4%) of the Ru/GA. These findings provide a simple method for increasing the instantaneous concentration of reactants around the catalyst, which in turn increases the reaction rate. The catalytic performances of composites subjected to different pretreatment conditions are also investigated. Hopefully, this finding may provide a feasible direction for the effective management of the diverse environment issues.

Recently, organic-inorganic hybrid perovskites (OIHP) are studied in memory devices, but ternary resistive memory with three states based on OIHP is not achieved yet. In this work, ternary resistive memory based on hybrid perovskite is achieved with a high device yield (75%), much higher than most organic ternary resistive memories. The pseudohalide-induced 2D (CH3 NH3 )2 PbI2 (SCN)2 perovskite thin film is prepared by using a one-step solution method and fabricated into Al/perovskite film/indium-tin oxide (glass substrate as well as flexible polyethylene terephthalate substrate) random resistive access memory (RRAM) devices. The three states have a conductivity ratio of 1:103 :107 , long retention over 10 000 s, and good endurance properties. The electrode area variation, impedance test, and current-voltage plotting show that the two resistance switches are attributable to the charge trap filling due to the effect of unscreened defect in 2D nanosheets and the formation of conductive filaments, respectively. This work paves way for stable perovskite multilevel RRAMs in ambient atmosphere.

Improving organic devices via molecular design is challenging and difficult to rationalize because individual molecular properties always convolute with intermolecular interaction and crystallinity to contribute the device performance. In this work, it is demonstrated for the first time that racemic effect can be utilized to effectively improve memory device performance. A pair of enantiomers and their mixture are used to prepare organic multilevel resistive random access memory (RRAM) devices. The RRAM devices fabricated from the equimolar mixture of enantiomers are of the lowest onset voltages and highest ternary device yield, independent of the preparation methods. Structural analysis of the powder, film, and single crystal of the equimolar mixture reveals formation of a real racemic compound, where π–π stacking in contrast to the only C–H–π interaction in the film of pure enantiomers appears. Since individual enantiomer has identical electronic properties, the discrepancy in device performance is attributed to the different intermolecular interactions.

Ternary resistive random access memory (RRAM) devices are fabricated from 1D d-π conjugated coordination polymer chains, which are synthesized via the coordination between Ni(II) salts and benzenetetramine or 3,3′,4,4′-biphenyltetramine in a solution process. The as-fabricated devices can retain their memory states for as long as three months at room temperature or work for at least 10 000 s at 150 °C, which is the highest working temperature reported for a ternary RRAM at the time of writing this paper. Thermogravimetric analysis indicates good thermal stability of these two materials because of their good crystallinity and strong intermolecular interaction. The long-term and high-temperature stability makes 1D conjugated coordination polymer chains a promising candidate for use as next-generation material for high-density data storage via RRAM techniques.

An organic thin-film gas sensor based on squaraine detects ammonia as low as 40 ppb with impressive reversibility and stability. The resonance-stabilized zwitterionic characteristics offer squaraines high affinity and sensitivity toward electron-rich analytes without irreversible chemical binding, while the embedded squaric ring makes SA-CH3 highly sensitive. The symmetric molecular geometry and good crystallinity also contribute to the high performance.

Organic resistive memory devices have been considered as potential candidates for next-generation, non-volatile memories. As prerequisites for real applications such memory devices would need to attain a high storage density, low power consumption, and, especially, long-term stability. Although extensive research has been carried out these issues have thus far not been resolved in a satisfactory manner. In this work, two phenothiazine-cored, cyano-substituted diphenylethene derivatives with trifluoromethyl and nitro-groups (PTZ-CF3 and PTZ-NO2) are presented and the performance of electroresistive memory devices based on these two molecules is investigated. Both molecules can realize ternary memory data storage with ternary device yields as high as 70%. In addition, PTZ-CF3-based devices exhibit a long-term stability (up to three months), lower operating voltage (−1.01/−2.42 V), and higher ON/OFF ratios (>104 and 103) compared to those based on PTZ-NO2. Such superior performance can be attributed to the introduced trifluoromethyl group, which leads to a better solubility, film-forming ability, and hydrophobicity. These results may serve as a guide to improve the performance and promote the development of organic memories.

Advanced materials with intelligent switchable surfaces that can respond to external stimuli have encouraging application in oil/water separation and oil clean-up. Herein, a facile method has been demonstrated to prepare a robust and superhydrophobic sponge by integrating the melamine-formaldehyde (MF) sponge with light-responsive spiropyran derivative via a radical copolymerization process, which shows the light-controllable oil absorption and desorption property under light illumination. The key chemistry is that the MF sponge is first modified with vinyl for the copolymerization via a facile solution-immersion process. Afterward, light-responsive spiropyran methacrylate monomers are copolymerized with vinyl-modified MF sponges to fabricate polymer-MF sponge composites (denoted as SP-MF sponge), resulting in the wettability conversion from amphiphilic to superhydrophobic with a water contact angle of 155.5°. The superhydrophobic MF sponge shows excellent selectivity and high absorption capacity for a range of oils and organic solvents from 70 to 154 times its own weight. More importantly, since the hydrophobic polymer of the SP-MF sponge can be converted to hydrophilic under UV illumination, the wettability of SP-MF sponge will change to hydrophilic, resulting in the light-controlled oil desorption process. These findings offer a new responsive absorbent material and a new approach for oil recovery.