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A novel mixed metal oxide of CuNiO x has been successfully obtained via electrosynthesis and thermal conversion of a Hofmann-type MOF Cu(pz) 2 [Ni(CN) 4 ] (pz = pyrazine). CuNiO x has demonstrated a significant enhancement in light absorption within a visible light range, leading to an impressive increase in photocurrent density and photocatalytic activity during light irradiation compared to CuO. The exceptional photoelectrochemical properties of the photocathodes of CuNiO x have been studied using multiple photoelectrochemical instrumental techniques, which proved the electrodes were stable over the whole water photolysis. The coupling of two metal centers has explained their outstanding performance. • A novel CuNiO x photocathode derived from Hofmann-type MOF was prepared. • CuNiO x shows significant improvement in photocatalytic activity towards H 2 production. • CuNiO x outperforms CuO in hydrogen evolution due to Cu-Ni synergy. • Spectroscopic studies highlight CuO and NiO roles in charge separation. [ABSTRACT FROM AUTHOR]

The discovery of single-atom catalysts (SACs) represents a groundbreaking advancement in the field of catalysis over the past decades. With the in-depth exploration of relevant structure-activity relationships, the metal-support interaction (MSI) is widely adopted to elucidate variations in electronic structure and coordination configuration of atomic active sites on various kinds of supports. Herein, we briefly summarize the metal oxide supports for SACs fabrication, including the distinctive characteristics of metal oxide supports, enlightening advancements in metal oxide support-based SACs (MO-SACs), feasible preparation methods for MO-SACs and effective regulation strategies of MSI effect in MO-SACs. In addition, we present our viewpoints and outlook in this field to stimulate rational design and construction of novel MO-SACs applied in diverse renewable energy devices, while some universal suggestions are sincerely given to provoke thoughtful considerations during the research process. [ABSTRACT FROM AUTHOR]

Blister-based laser-induced forward transfer (BB-LIFT) is a promising high precision and resolution printing technique for the fast, solvent- and mask-free transfer of functional layered materials onto micro-devices. It utilizes a protective metal (blister) layer sandwiched between the laser-transparent substrate and the material to be transferred. The metal layer absorbs the incident laser pulse, creating a rapidly expanding blister that propels the overlying material onto a target substrate. We show that BB-LIFT of thin and ultrathin (30 and 3 nm) ZrO2 films is realized only with a "graphene release layer" applied between the Al blister layer and the ZrO2 donor layer. Without such intercalation, ZrO2 is inseparable from the blister layer due to the strong oxide bonding with aluminum oxides formed during the preparation. The ZrO2 transfer was confirmed through high-resolution scanning electron microscopy and energy-dispersive X-ray spectroscopy, affirming the critical role of graphene as a release layer. The promotion of mechanically strong, flexible graphene as a release layer can be generalized in BB-LIFT applications if thin films of fragile, polycrystalline, or amorphous metal oxides must be printed for gas sensors, catalytic, or other applications. [ABSTRACT FROM AUTHOR]

K3Li2Ta5O15 is found as a novel photocatalyst for overall water splitting under ultraviolet light irradiation. K3Li2Ta5O15 possesses a characteristic crystal structure with Li+ ion-filled C-sites in (A1)4(A2)2C4M10O30 as the general formula of a tungsten bronze-type metal oxide. Most of the reported photocatalysts with a tungsten bronze structure possess empty C-sites. K6Ta10.8O30 also possesses a C-site-filled tungsten bronze structure in which C-sites are partially filled with Ta5+ ions. In diffuse reflectance spectra, K6Ta10.8O30 has an absorption edge at a longer wavelength than K3Li2Ta5O15. This narrower band gap of K6Ta10.8O30 than K3Li2Ta5O15 is considered to be due to the presence of Ta5+ ions at C-sites in K6Ta10.8O30. Ta5+ ions that are located at 9-fold coordination C-sites with a totally different surrounding environment from the 6-fold coordination M-sites will form the conduction band minimum at a lower potential than those located at 6-fold coordination M-sites. The optimized K3Li2Ta5O15 shows almost the same water-splitting activity as the optimized K6Ta10.8O30. Thus, it is found that the conduction band that is formed by Ta5+ ions at C-sites is also effective for photocatalytic reaction, being similar to that formed by Ta5+ ions at M-sites. [ABSTRACT FROM AUTHOR]

Blister-based laser-induced forward transfer (BB-LIFT) is a promising high precision and resolution printing technique for the fast, solvent- and mask-free transfer of functional layered materials onto micro-devices. It utilizes a protective metal (blister) layer sandwiched between the laser-transparent substrate and the material to be transferred. The metal layer absorbs the incident laser pulse, creating a rapidly expanding blister that propels the overlying material onto a target substrate. We show that BB-LIFT of thin and ultrathin (30 and 3 nm) ZrO2 films is realized only with a "graphene release layer" applied between the Al blister layer and the ZrO2 donor layer. Without such intercalation, ZrO2 is inseparable from the blister layer due to the strong oxide bonding with aluminum oxides formed during the preparation. The ZrO2 transfer was confirmed through high-resolution scanning electron microscopy and energy-dispersive X-ray spectroscopy, affirming the critical role of graphene as a release layer. The promotion of mechanically strong, flexible graphene as a release layer can be generalized in BB-LIFT applications if thin films of fragile, polycrystalline, or amorphous metal oxides must be printed for gas sensors, catalytic, or other applications. [ABSTRACT FROM AUTHOR]

Metal-organic framework (MOF) derived metal oxide nanostructures hold immense promise as electrodes for energy storage/conversion applications, notably in supercapacitors and urea oxidation. This study explores into optimizing such nanostructures, specifically focusing on a Zr/Ni ratio of 1:1, which has exhibited favorable electrochemical and catalytic performance. Employing thorough characterization methods, including PXRD analysis, we verified the successful synthesis of a ZrO 2 /NiO binary phase (i.e. Zr/Ni) nanostructure via the MOF-derived approach, showcasing its versatility as a catalyst across diverse energy conversion domains. The Zr/Ni nanostructure electrode displayed noteworthy characteristics, boasting a capacity of 432 C/g alongside exceptional cycling stability of 99%, reflecting battery-like electrochemical behavior. Furthermore, in an asymmetric device setup (Zr/Ni//AC), it achieved a notable potential of up to 1.4 V with an impressive power density of 1044.56 W/kg. Additionally, the Zr/Ni nanostructure demonstrated efficient electrocatalytic activity in urea oxidation, evidenced by a maximum current density of 60 mA/cm2. This underscores its viability as a preferred catalyst in energy conversion applications, signaling opportunities for further exploration and advancement in this dynamic field. [Display omitted] • Successful formation of a binary phase of Zr/Ni nanostructure achieved by single step route. • Zr/Ni nanostructure demonstrated a specific capacity of 432C/g. • Zr/Ni//AC device showed ED of 4.08 Wk/g@ 420 W/kg. • Zr/Ni nanostructure exhibits a low onset voltage (1.34 V) in urea oxidation. • Zr/Ni nanostructure shows the highest current density of 60 mA/cm2. [ABSTRACT FROM AUTHOR]

This study presents the synthesis of a multicomponent metal oxide electrocatalyst that increases the activity of the oxygen evolution reaction (OER). We synthesized transition metal oxides (MnOx, FeOx, CoOx, and NiOx) with MoO3 heterostructures through a solid-state reaction approach at low cost. In comparison to the other compositions, CoOx garnered higher attention and demonstrated superior performance on account of its large surface area and varied crystal facets. The MnOx-MoO3, FeOx-MoO3, CoOx-MoO3, and NiOx-MoO3 compositions attained an overpotential of 390 mV, 350 mV, 310 mV, and 340 mV, respectively, at a current density of 10 mA cm−2 in alkaline solution. The performance of OER was enhanced in CoOx-MoO3 at 10 mA cm−2, while FeOx-MoO3 exhibited a lower current density at 100 mA cm−2 than other metal oxides. The CoOx-MoO3 material exhibited a favorable crystal interface transition due to the presence of MoO3 oxide. For the first time, we report on the MoO3-to-(MnOx, FeOx, CoOx, and NiOx) interface crystal transition and the active surface area for OER catalytic activity in water-splitting processes. This investigation intends to develop an electrocatalyst that is capable of producing hydrogen with the use of heterostructure metal oxides. [ABSTRACT FROM AUTHOR]

Biopolymer blend based nanocomposites have been interestingly investigated by researchers to achieve advanced composite functional materials that are environmentally amicable. Among the varieties of biopolymers, widespread attention has been given to polyvinyl alcohol (PVA) and polyvinyl pyrrolidone (PVP) owing to their interesting properties like water solubility, biodegradability, biocompatibility and non-toxicity. PVA and PVP form a completely miscible blend at all compositions as both the polymers are rich in a variety of functional groups that permit effective intermolecular interactions between the polymers as well as with filler. PVA/PVP blend exhibits excellent dopant sensitive properties also. Metal oxide nanoparticles (MONPs) have made a prominent place in the area of scientific and technological research due to their unique chemical and physical properties. Doping with MONPs enhances the properties of the PVA/PVP blend matrix and the resulting PVA/PVP/MONP polymer nanocomposites are suitable for multifunctional purposes. This review mainly focused on the influence of various MONPs such as ZnO, CuO, Al2O3, ZrO2, MnO, SnO, MgO, TiO2, etc. in the structural, morphological, thermal, optical and electrical properties of PVA/PVP blend as well as its applications in various fields. [ABSTRACT FROM AUTHOR]

• Wider variety of artefacts needs to be conserved. • NPs based coating have the potency to replace the traditional coating materials. • The NPs improved the photo-catalysis, hydrophobicity and antibacterial properties. The progression in the use of nanostructured metal oxide or metal oxide based polymeric nanocomposite for the conservation and refurbishment of cultural heritage are presented in this review. Starting from the definition of nanoparticles, their major synthesis techniques, the paper briefly describes the utilization of various metal oxide nanoparticles and metal oxide based polymeric nanocomposite coatings and their surface protection functions including self-cleaning, increased photocatalytic activity, biocidal effects, UV blocking properties and compatibility with the different types of substrates including wood, stones, bricks and paper focussing on their potential usage and their application in the arena of remediation of cultural heritage. [Display omitted] [ABSTRACT FROM AUTHOR]

Humidity is a well-known interference factor in metal oxide (MOX) gas sensors, significantly impacting their performance in various applications such as environmental monitoring and medical diagnostics. This study investigates the effects of adsorbed water on MOX conductivity using two different materials: pure tin oxide (SnO2) and a tin–titanium–niobium oxide mixture (SnTiNb)xO2 (STN). The results reveal that (SnTiNb)xO2 sensors exhibit reduced sensitivity to humidity compared to pure tin oxide, rendering them more suitable for applications where humidity presence is critical. We aimed to shed light on a still controversial debate over the mechanisms involved in the water surface interactions for the aforementioned materials also by exploring theoretical studies in the literature. Experimental analysis involves varying temperatures (100 to 800 °C) to understand the kinetics of surface reactions. Additionally, a brief high-temperature heating method is demonstrated to effectively remove adsorbed humidity from sensor surfaces. The study employs Arrhenius-like plots for graphical interpretation, providing insights into various water adsorption/desorption phenomena. Overall, this research contributes to a deeper understanding of the role of humidity in MOX gas sensor mechanisms and offers practical insights for sensor design and optimization. [ABSTRACT FROM AUTHOR]

The textile industry is consistently integrating cutting-edge technologies, introducing materials with multifaceted features, such as odour resistance, hydrophobicity, durability, and self-cleaning capabilities. This transformation is facilitated by the application of nanotechnology. The focal point of this experimental endeavour lies in closing the gap in employing ZnO nanoparticles on high GSM denim fabric, enhancing self-cleaning, UV protection, and antimicrobial capabilities. Initially, a solution containing nanoparticles, binder, softener, ethanol, and their auxiliaries was formulated. Zinc oxide nanoparticles, along with their auxiliaries, were applied to the denim using the pad-dry-cure and pad-dry-steam methods. Various trials were conducted to optimize the concentration of ZnO NPs, with the formulation containing 5% ZnO NPs, 5% binder, and 25% ethanol. Experimentation ensued to establish optimal time-temperature profiles for drying, curing, and steaming. Comprehensive evaluations, including drop tests, stain tests, colour strength assessments, crocking tests, SEM analysis, antimicrobial testing and UV protection factor determination were conducted on the samples. The study revealed that fixation of the self-cleaning finish by curing gives better results than by steaming. SEM examination highlighted the distribution of ZnO nanoparticles on the denim fabric. Lastly, antimicrobial properties were assessed, concluding that treated fabrics exhibited antibacterial activity compared to untreated fabrics. [ABSTRACT FROM AUTHOR]

In this study, the results of the investigation of the influence of Al atoms on the structural characteristics of ZnO films obtained by the sol- gel method are presented. It has been determined that the glass substrates consist of subcrystallites with dimensions of 28.6 nm, having cubic unit cells with lattice parameters a = 0.3336 nm, and their surfaces belong to the crystallographic orientation (111). It has been identified that the grown thin ZnO films consist of subcrystallites with dimensions of 39.5 nm, having a wurtzite structure with lattice parameters a = b = 0.3265 nm and c = 0.5212 nm, respectively. It has been determined that at the boundaries of the division of these subcrystallites, polycrystalline regions with sizes of 12.6 nm, 28.3 nm, 30 nm, and 33 nm are formed. Additionally, nanocrystallites with sizes of 56.8 nm self-assemble on the surface areas of the deposited films. The increase in the values of the "c"axis of the hexagonal crystal lattice of ZnO films by 0.0009 nm when doping Al atoms from 1% to 5% is explained by the shift of the main structural line (002) at small angles (40-0.12°). It has been established that nanocrystallites with lattice parameters an = 0.5791 nm, belonging to the spatial group Fd3m, self-assemble on the surface areas of ZnO:Al films. the curve due to the presence of a monoenergetic level of fast surface states at the heterojunction. [ABSTRACT FROM AUTHOR]

[Display omitted] • Desulfurization in waste tire pyrolysis oil and gas was achieved by metal oxides. • Fe 2 O 3 shows the best removal efficiency of 87.7% for sulfur-containing gas. • The desulfurization mechanism was revealed by ReaxFF-MD and experiments analysis. • The removal of S involved Fe-S bonding, C-S breakage, dehydrogenation, O migration. • Fe 2 O 3 promotes cyclization and dehydrogenation to produce monoaromatics (57.4%). Pyrolysis can effectively convert waste tires into high-value products. However, the sulfur-containing compounds in pyrolysis oil and gas would significantly reduce the environmental and economic feasibility of this technology. Here, the desulfurization and upgrade of waste tire pyrolysis oil and gas were performed by adding different metal oxides (Fe 2 O 3 , CuO, and CaO). Results showed that Fe 2 O 3 exhibited the highest removal efficiency of 87.7 % for the sulfur-containing gas at 600 °C with an outstanding removal efficiency of 99.5 % for H 2 S. CuO and CaO were slightly inferior to Fe 2 O 3 , with desulfurization efficiencies of 75.9 % and 45.2 % in the gas when added at 5 %. Fe 2 O 3 also demonstrated a notable efficacy in eliminating benzothiophene, the most abundant sulfur compound in pyrolysis oil, with a removal efficiency of 78.1 %. Molecular dynamics simulations and experiments showed that the desulfurization mechanism of Fe 2 O 3 involved the bonding of Fe-S, the breakage of C-S, dehydrogenation and oxygen migration process, which promoted the conversion of Fe 2 O 3 to FeO, FeS and Fe 2 (SO 4) 3. Meanwhile, Fe 2 O 3 enhanced the cyclization and dehydrogenation reaction, facilitating the upgrade of oil and gas (monocyclic aromatics to 57.4 % and H 2 to 22.3 %). This study may be helpful for the clean and high-value conversion of waste tires. [ABSTRACT FROM AUTHOR]

The chief source of water pollution is industrial wastewater containing dyes. In current study, the optimum conditions for removal of Red-XGRL dye by green metal oxide polymeric nanocomposites were determined via batch and column study. The synthesized materials were characterized via SEM, FTIR and thermal analysis. The optimum pH for attaining maximum adsorption capacity of WD, WD-ZnO-PTh, WD-ZnO-PAN and WD-ZnO-PPY was found to be 8 (12.9 mg/g), 10 (30.2 mg/g), 11 (35.8 mg/g) and 11 (40 mg/g), respectively, and optimum dose was found to be 0.05 g/50 mL. The highest adsorption potential for all composite materials was attained within 90 min and maximum adsorption potential for WD (40.8 mg/g), WD-ZnO-PTh (60.7 mg/g), WD-ZnO-PAN (70.4 mg/g) and WD-ZnO-PPY (86.3 mg/g) was obtained using 200 mg/L dye concentration at 30 °C. The adsorption data showed better fitness to pseudo-second-order kinetics and Langmuir sorption isotherm giving significant R2 values of 0.95–0.99 and 0.97–0.99, respectively. Thermodynamic study showed exothermic nature of sorption. During column study, optimum adsorbent bed height, dye flow rate and inlet initial dye concentration to attain highest adsorption (35 mgg−1) were determined to be 3 cm, 1.8 mL min−1 and 70 mg/L, respectively. Hence, the present study aimed to remove Red-XGRL dye proved that these green metal oxide polymeric nanocomposites could efficiently be synthesized and utilized for efficient removal of Red-XGRL dye from aqueous solution both in batch and in column mode. [ABSTRACT FROM AUTHOR]

In recent years, research on improving the synthesis of catalysts has been at the forefront because of advancements in nanotechnology and greener conventions. Using ultrasound (US) during nanocatalysts synthesis is one of the green approaches that can yield improved catalyst characteristics under conditions of shorter reaction time and requirement of low temperature and pressure. The current paper aims at giving an insight into US‐assisted synthesis (emphasized on sol‐gel and hydrothermal) of different metal oxide nanocatalysts. It has been elucidated that US‐assisted synthesis gives nanocatalyst with narrower particle size distribution with lower mean size, higher surface area, better morphology with less agglomeration, and higher catalytic activity. Ultrasound has thus been demonstrated to yield improvements in morphological, optical, and electronic properties of the nanocatalysts, however, scalability and industrial application of sonochemical synthesis have not been seen very popular. Some guidelines for future research into the development of novel nanocatalysts and industrial scale‐up studies are also provided. The review also summarizes the application of these metal oxides as photocatalysts for dye degradation or effluent treatment containing dyes, highlighting the fundamentals of photocatalysis as well. A comparative study has been reported for catalysts obtained using the US‐assisted synthesis and conventional synthesis of the photocatalysts in terms of catalytic activity. The benefits of using ultrasound‐assisted synthesis in terms of higher photocatalytic degradation have been clearly demonstrated. [ABSTRACT FROM AUTHOR]

A low‐temperature technology for fabricating thin‐film transistors (TFTs) is essential for the realization of electronic systems on flexible substrates. Presently reviewed are improved techniques for forming the source/drain regions and reducing the population of channel defects in a metal‐oxide TFT. These have been applied to the construction of different TFT structures, including ones with bottom gate, top gate, and dual gates. The utility of the improved 300‐°C technology has been demonstrated by the realization of a variety of electronic systems, such as a gate‐driver on array for active‐matrix displays, an analog front‐end for acquiring biopotential signals, and an artificial neural network for neuromorphic computing. [ABSTRACT FROM AUTHOR]

The 13.2 inch AMOLED panel with 262 ppi has been fabricated with the high mobility metal oxide TFTs (thin film transistors). The high mobility oxide TFTs have high mobility ~34cm2 /Vs. On Gen. 6 glass, a small Vth variation with channel length 3.5um has been obtained. Moreover, the high mobility oxide TFT shows small Vth shift under positive/negative bias temperature stress (PBTS/NBTS). [ABSTRACT FROM AUTHOR]

This study proposes a new modification of lignocellulosic biomass based on apricot kernel shells with composite activation KI/KOH and functionalized with a tolerant material (MgO) powder. Apricot kernel shells (NAK), modified apricot kernel shells (MAK) and doped apricot kernel shells (DAK) obtained were characterized using various methods, such as infrared spectroscopy (FTIR), scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDX), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and point of zero charge (pHpzc). The adsorbents were also evaluated in batch adsorption, using basic fuchsine dye (BF) to determine the performance and specific capacity of the adsorption process. The results showed that only 90 min and 0.1 g of DAK or MAK are sufficient to remove 93% and 91%, respectively, of basic fuchsine from aqueous solutions with a concentration of 20 mg/L in a volume of 100 mL. The MAK and DAK adsorbents can be reused for 5 cycles before their yield decreases below 50%, without requiring complex regeneration procedures, only drying for 4 h at 105°C. The evolution of adsorption was analyzed under different parameters, such as contact time, initial dose of adsorbent, initial dye concentration, initial pH, and temperature. The kinetic adsorption models indicate that the pseudo-second-order model was more suitable than the pseudo-first-order and intraparticle diffusion models for describing the adsorption process. The equilibrium adsorption data of BF were better fitted by the Langmuir isotherm, compared to the Freundlich and Temkin isotherms. [ABSTRACT FROM AUTHOR]

A series of metal- and silica-containing carbon-based nanocomposites were synthesized by pyrolysis of a resorcinol–formaldehyde polymer modified with metal oxide/silica nanocomposites (MxOy/SiO2, where M = Mg, Mn, Ni, Cu and Zn) via the thermal oxidative destruction of metal acetates adsorbed on highly dispersed silica (A380). The concentration of metals was 3.0 mmol/g SiO2. The phase composition and morphological, structural and textural properties of the carbon materials were analyzed by X-ray diffraction, SEM, Raman spectroscopy and low-temperature N2 adsorption. Thermal decomposition under a nitrogen atmosphere and in air was analyzed using TG–FTIR and TG–DTG–DSC techniques to determine the influence of the filler on the decomposition process. The synthesized composites show mesoporous structures with high porosity and narrow pore size distributions. It could be shown that the textural properties and the final composition of the nanocomposites depend on the metal oxide fillers of the precursors. The data obtained show that nickel and copper promote the degree of graphitization and a structural order with the highest porosity and largest specific surface area of the hybrid composites. The good adsorption properties of the obtained materials were shown for the recovery of p-chlorophenol and p-nitrophenol from aqueous solutions. [ABSTRACT FROM AUTHOR]

As a stable, low-cost, environment-friendly, and gas-sensitive material, semiconductor metal oxides have been widely used for gas sensing. In the past few years, single-atom catalysts (SACs) have gained increasing attention in the field of gas sensing with the advantages of maximized atomic utilization and unique electronic and chemical properties and have successfully been applied to enhance the detection sensitivity and selectivity of metal oxide gas sensors. However, the application of SACs in gas sensors is still in its infancy. Herein, we critically review the recent advances and current status of single-atom catalysts in metal oxide gas sensors, providing some suggestions for the development of this field. The synthesis methods and characterization techniques of SAC-modified metal oxides are summarized. The interactions between SACs and metal oxides are crucial for the stable loading of single-atom catalysts and for improving gas-sensitive performance. Then, the current application progress of various SACs (Au, Pt, Cu, Ni, etc.) in metal oxide gas sensors is introduced. Finally, the challenges and perspectives of SACs in metal oxide gas sensors are presented. [ABSTRACT FROM AUTHOR]

Electron and hole transporting layers play a major role in high-performance and stable organic-based optoelectronic devices. This paper demonstrates detailed device engineering of multi-junction organic photovoltaics built on two different metal oxide-based electron and hole transport (buffer) layers prepared by thermal or solution-processed methods. The main focus is on the device processing parameters as well as practical details of preparation of buffer layers to give the research community a clear, step-by-step recipe to successfully replicate and build series and parallel connected multi-junction solution-based organic solar cells for their needs. Here, the recipes and deposition conditions of two metal oxide buffer layers are presented in detail, based on basic commercially available materials and tools, to achieve well-engineered tandem (multi-junction) solution-processed organic solar cells. The buffer layers have appropriate energy levels for electrical selectivity of anode and cathode electrodes, and they are highly stable and chemically compatible with processing of solution-based polymer solar cells. To demonstrate the engineering steps of multi-junction devices, the PCE10:PC70BM blend is used as the active layer for all subcells. Then, to improve the power conversion efficiency of the single-junction photovoltaic device, PCE10:PC70BM blend is used in combination with DPPx:PC70BM with different absorption spectra for bottom and top subcell active layers. An optimized series tandem device with 10.6% power conversion efficiency is demonstrated. Generally, the device structures reported here can also be used for other types of optoelectronic devices, such as light emitting diodes and photodetectors. [ABSTRACT FROM AUTHOR]

Graphene/metal oxide (rGO/MOx) heterostructures hold great promise for energy storage, yet a full understanding of their synthesis remains elusive. Herein, a general, efficient, and scalable synthesis strategy is designed for the preparation of various rGO/MOx heterostructure materials featuring robust interfacial interactions. The heterogeneous nucleation growth mechanism of metal oxides on graphene is elucidated through ex situ characterization and theoretical simulation. The surface of graphene oxide (GO) is enriched with reactive oxygen‐containing functional groups, serving as potent nucleation sites that facilitate the rapid and heterogeneous nucleation of MOx grains. Simultaneously, a stable interface (C−O−M bond) is in situ formed between graphene and adsorbed metal ions during heat treatment, producing rGO/MOx heterostructure materials. Notably, the resultant rGO/CoO heterostructure material is employed as an anode and LiCoO2 as a cathode to assemble a soft packaging quasi‐solid‐state battery, which has demonstrated an impressive energy density of 341.4 Wh kg−1 and maintains outstanding capacity retention at 93.4% after 300 cycles at a 1C current. These findings provide valuable insights into the preparation and potential applications of rGO/MOx heterostructure materials for energy storage. [ABSTRACT FROM AUTHOR]

Over the years, metal oxides have been leveraged to create several intriguing novel antibacterial active materials such that while finding the ways and means to increase efficiency, rare earth elements are found to have often served as potential optical dopants such that an optimistic en route to achieve the same, branched Sm‐doped CuO nano‐lanceolates were synthesized employing a wet chemical approach. The samples were then annealed at three distinct temperatures, which were fixed to 300 °C, 400 °C, and 500 °C. The nano‐lanceolates have crystallized in the monoclinic phase, according to the XRD analysis. The SEM image of Sm‐doped CuO captured at a magnification of 2 μm reveals a branched morphology, with multiple nano‐lanceolates stacked in a stem. TEM image reveals that the width of a typical nano‐lanceolate attached to a stem and its tip are found to be 87 nm and 212 nm, respectively and the obtained EDS data validate that elements including Cu, Sm, and O are present in the doped sample. The UV‐visible spectra of the annealed samples indicate that the sample annealed at 300 °C (1.43 eV) has a larger band gap than the other samples. The sample that was annealed at 400 °C has endured defect emissions that are more intense than those of other samples, according to the obtained PL spectra. In addition to these fascinating findings, the samples annealed at 300 °C, 400 °C and 500 °C exhibit a zone of inhibition of 23 mm & 24 mm, 11 mm & 12 mm and 12 mm & 11 mm, respectively for the two tested bacterial strains which authenticate that the 300 °C annealed Sm‐doped CuO nano‐lanceolate deactivates the two pathogenic bacteria more effectively compared to the other samples. As a consequence, the Sm‐doped CuO nano‐lanceolates at 300 °C could potentially be an effective alternative for antibacterial materials, particularly in biomedical applications [ABSTRACT FROM AUTHOR]

This article discusses the main trends in the physics and preparation of metal oxides and summarizes the results of research published by SPQEO in this area over the past decade. The main metal oxides studied include ZnO, Zn1-xCdxO, Zn1-xCoxO, MgxZn1– xO, ZnO:Mn, VO2, ZrO2–Y2O3, TiO2, WO3, Gd2O3, Er2O3, WO3–CaO–SiO2–B2O3: Tb3+, Dy2O3, NiO, FexOy, Ga2O3, Al2O3, ITO, Ag2O and graphene oxide. These oxides were obtained by the following methods: sintering in air or in a stream of various gases, magnetron sputtering, atomic layer deposition, explosive evaporation, sol-gel, spin coating, spray pyrolysis, rapid thermal annealing, green synthesis from plant solutions, melt quenching, rapid thermal annealing, self-ignition, ion-plasma co-sputtering, vacuum sputtering, reactive ion beam sputtering, and the Hammer method. The electrical and optical properties of the studied oxides are illustrated. [ABSTRACT FROM AUTHOR]

Due to their encouraging results, nanolubricants have been revolutionary in the field of lubrication. The degree, to which the new material may improve the tribology, energy savings, and durability, is a crucial consideration for any new additive to a conventional lubricant. The results of the earlier research on carbon, metal, metal oxide, and their composites and hybrid nanolubricants as well as their effects on tribology, are summarized in this review paper. The most popular measuring methodologies, the tribology results for lubricants with an oil base, biodegradable base, and a water base, as well as the reasons that explain these tribological advancements, are all included in this study. Finally, prospects for more study in this area are emphasized. [ABSTRACT FROM AUTHOR]

Organic–inorganic halide perovskites are widely investigated for various optoelectronics devices such as photodetectors and solar cells. However, Pb‐based perovskite photodetectors perform poorly because of insufficient mobility and absence of an effective photoconductive gain mechanism. Herein, ZnON/perovskite heterostructures are demonstrated to realize the fabrication of high‐performance hybrid phototransistors. Additionally, a guanidinium iodide (GuI), alternating‐cation‐interlayer (ACI)‐type organic spacers, are utilized as an interface passivation layer. It is shown that the GuI interface layer reduces the defect density of the ZnON surface as well as the bulk perovskite film and promotes the separation and transport of photo‐generated charge carriers. Devices fabricated with the GuI interface passivation layer have a response speed of 0.1 s, excellent responsivity of 5.97 × 106 A W−1, and ultra‐high specific detectivity of 1.28 × 1018 Jones, the highest value among previously reported perovskite‐based hybrid phototransistors. This work provides valuable insights into the design and fabrication of high‐performance metal oxide/perovskite heterostructures with promising applications in future optoelectronic devices. [ABSTRACT FROM AUTHOR]

Graphene and its derivatives have been confirmed to be among the best fillers for rubber due to their excellent properties, such as high mechanical strength, improved interface interaction, and strain-induced crystallization capabilities. Graphene rubber materials can be widely used in tires, shoes, high-barrier conductive seals, electromagnetic shielding seals, shock absorbers, etc. In order to reduce the graphene loading and endow more desirable functions to rubber materials, graphene-based hybrid fillers are extensively employed, which can effectively enhance the performance of rubber composites. This review briefly summarizes the recent research on rubber composites with graphene-based hybrid fillers consisting of carbon black, silica, carbon nanotubes, metal oxide, and one-dimensional nanowires. The preparation methods, performance improvements, and applications of different graphene-based hybrid fillers/rubber composites have been investigated. This study also focuses on methods that can ensure the effectiveness of graphene hybrid fillers in reinforcing rubber composites. Furthermore, the enhanced mechanism of graphene- and graphene derivative-based hybrid fillers in rubber composites is investigated to provide a foundation for future studies. [ABSTRACT FROM AUTHOR]

The search for new high-performance push-pull materials for use in nonlinear optics (NLO) and optics is currently a popular area of research. In this study, the effects of metal oxides -(MO)n = 1,2 (monomer: MO=TiO2, CuO, Al2O3, and ZnO; and dimer: MO = Ti2O4, Cu2O2, Al4O6, and Zn2O2) on the electronic, absorption, optoelectronic and NLO characteristics of circumcorannulene (CO) in the gas phase and in acetonitrile have been investigated using density functional theory (DFT) and time-dependent density functional theory (TD-DFT) at the B3LYP and CAM-B3LYP/6-311+G(d,p)/LANL2DZ levels of theory. Research has shown that adding metal oxides to CO leads to the formation of new push-pull CO derivatives. These derivatives include T1, U1, A1, Z1, T2, U2, A2, and Z2 formed from TiO2, CuO, Al2O3, ZnO, Ti2O4, Cu2O2, Al4O6, and Zn2O2 metal oxides, respectively. They exhibit excellent stability, low |HOMO-LUMO| gap energy, high NLO, and photocurrent responses compared to CO in gaseous media and polar solvents. However, it is interesting to note that the use of the copper oxide monomer configuration on corannulene family compounds is effective in improving their NLO response, while increasing the alumina chain proves necessary to improve their photocurrent response in the visible region. [ABSTRACT FROM AUTHOR]

Polysiloxane dielectric elastomers have garnered a considerable deal of attention over the last decade due to their potential as electroactive soft materials. However, the intrinsic low dielectric constant of polysiloxanes has proven a serious limitation in their practical use. In this work, we controlled the dielectric properties of silicone rubber composites by changing the type and content of oxide fillers. The silicone‐based dielectric elastomers with a high dielectric constant (5.21@1 kHz), low modulus (1.62 MPa), and high elongation (1100%) were successfully obtained. The effects of different types of metal oxides on the dielectric properties and mechanical properties of the prepared composites are further explored. Due to their excellent comprehensive features, these types of materials are expected to be applied in capacitive sensors, actuators, generators, and beyond. [ABSTRACT FROM AUTHOR]

The binary metal oxide mesoporous interfacial layers (bi-MO meso IF layer) templated by a graft copolymer are synthesized between a fluorine-doped tin oxide (FTO) substrate and nanocrystalline TiO2 (nc-TiO2). Amphiphilic graft copolymers, Poly(epichlorohydrin)-graft-poly(styrene), PECH-g-PS, were used as a structure-directing agent, and the fabricated bi-MO meso IF layer exhibits good interconnectivity and high porosity. Even if the amount of ZnO in bi-MO meso IF layer increased, it was confirmed that the morphology and porosity of the bi-MO meso IF layer were well-maintained. In addtion, the bi-MO meso IF layer coated onto FTO substrates shows higher transmittance compared with a pristine FTO substrate and dense-TiO2/FTO, due to the reduced surface roughness of FTO. The overall conversion efficiency (η) of solid-state photovoltaic cells, dye-sensitized solar cells (DSSCs) fabricated with nc-TiO2 layer/bi-MO meso IF layer TZ1 used as a photoanode, reaches 5.0% at 100 mW cm−2, which is higher than that of DSSCs with an nc-TiO2 layer/dense-TiO2 layer (4.2%), resulting from enhanced light harvesting, good interconnectivity, and reduced interfacial resistance. The cell efficiency of the device did not change after 15 days, indicating that the bi-MO meso IF layer with solid-state electrolyte has improved electrode/electrolyte interface and electrochemical stability. Additionally, commercial scattering layer/nc-TiO2 layer/bi-MO meso IF layer TZ1 photoanode-fabricated solid-state photovoltaic cells (DSSCs) achieved an overall conversion efficiency (η) of 6.4% at 100 mW cm−2. [ABSTRACT FROM AUTHOR]

Due to the ongoing threat of degradation of artefacts and monuments, the conservation of cultural heritage items has been gaining prominence on the global scale. Thus, finding suitable approaches that can preserve these materials while keeping their natural aspect of is crucial. In particular, preventive conservation is an approach that aims to control deterioration before it happens in order to decrease the need for the intervention. Several techniques have been developed in this context. Notably, the application of coatings made of metal oxide nanomaterials dispersed in polymer matrix can be effectively address stone heritage deterioration issues. In particular, metal oxide nanomaterials (TiO2, ZnO, CuO, and MgO) with self-cleaning and antimicrobial activity have been considered as possible cultural heritage conservative materials. Metal oxide nanomaterials have been used to strengthen heritage items in several studies. This review seeks to update the knowledge of different kinds of metal oxide nanomaterials, especially nanoparticles and nanocomposites, that have been employed in the preservation and consolidation of heritage items over the last 10 years. Notably, the transport of nanomaterials in diverse environments is undoubtedly not well understood. Therefore, controlling their effects on various neighbouring non-target organisms and ecological processes is crucial. [ABSTRACT FROM AUTHOR]

As supercapacitor (SC) technology continues to evolve, there is a growing need for electrode materials with high energy/power densities and cycling stability. However, research and development of electrode materials with such characteristics is essential for commercialization the SC. To meet this demand, the development of superior electrode materials has become an increasingly critical step. The electrochemical performance of SCs is greatly influenced by various factors such as the reaction mechanism, crystal structure, and kinetics of electron/ion transfer in the electrodes, which have been challenging to address using previously investigated electrode materials like carbon and metal oxides/sulfides. Recently, tellurium and telluride‐based materials have garnered increasing interest in energy storage technology owing to their high electronic conductivity, favorable crystal structure, and excellent volumetric capacity. This review provides a comprehensive understanding of the fundamental properties and energy storage performance of tellurium‐ and Te‐based materials by introducing their physicochemical properties. First, we elaborate on the significance of tellurides. Next, the charge storage mechanism of functional telluride materials and important synthesis strategies are summarized. Then, research advancements in metal and carbon‐based telluride materials, as well as the effectiveness of tellurides for SCs, were analyzed by emphasizing their essential properties and extensive advantages. Finally, the remaining challenges and prospects for improving the telluride‐based supercapacitive performance are outlined. [ABSTRACT FROM AUTHOR]

In here, cobalt-zinc bimetallic oxides@polypyrrole (PPy) composites with core–shell structure are prepared, and the prepared Co 3 O 4 /ZnCo 2 O 4 @PPy (CZCP) has a wide absorption of 5.58 GHz, while ZnCo 2 O 4 /ZnO@PPy (ZCZP) has a strong reflection loss of −71.2 dB. [Display omitted] • By changing the ratio of Co2+ and Zn2+ of the MOF precursors, the various cobalt-zinc bimetallic oxides are fabricated. • Cobalt-zinc bimetallic oxides@polypyrrole (PPy) composites with core–shell structure are prepared through in situ polymerization method. • When the loading is 50 wt%, the EAB of Co 3 O 4 /ZnCo 2 O 4 @PPy is 5.58 GHz (12.42–18 GHz) at 1.53 mm, and the RL min of ZnCo 2 O 4 /ZnO@PPy is −71.2 dB at 13.04 GHz and 1.84 mm. Composite materials that combine magnetic and dielectric losses offer a potential solution to enhance impedance match and significantly improve microwave absorption. In this study, Co 3 O 4 /ZnCo 2 O 4 and ZnCo 2 O 4 /ZnO with varying metal oxide compositions are successfully synthesized, which are achieved by modifying the ratios of Co2+ and Zn2+ ions in the CoZn bimetallic metal–organic framework (MOF) precursor, followed by a high-temperature oxidative calcination process. Subsequently, a layer of polypyrrole (PPy) is coated onto the composite surfaces, resulting in the formation of core–shell structures known as Co 3 O 4 /ZnCo 2 O 4 @PPy (CZCP) and ZnCo 2 O 4 /ZnO@PPy (ZCZP) composites. The proposed method allows for rapid adjustments to the metal oxide composition within the inner shell, enabling the creation of composites with varying degrees of magnetic losses. The inclusion of PPy in the outer shell serves to enhance the bonding strength of the entire composite structure while contributing to conductive and dielectric losses. In specific experimental conditions, when the loading is set at 50 wt%, the CZCP composite exhibits an effective absorption bandwidth (EAB) of 5.58 GHz (12.42 GHz-18 GHz) at a thickness of 1.53 mm. Meanwhile, the ZCZP composite demonstrates an impressive minimum reflection loss (RL min) of −71.2 dB at 13.04 GHz, with a thickness of 1.84 mm. This study offers a synthesis strategy for designing absorbent composites that possess light weight and excellent absorptive properties, thereby contributing to the advancement of electromagnetic wave absorbing materials. [ABSTRACT FROM AUTHOR]

As technologies like the Internet, artificial intelligence, and big data evolve at a rapid pace, computer architecture is transitioning from compute-intensive to memory-intensive. However, traditional von Neumann architectures encounter bottlenecks in addressing modern computational challenges. The emulation of the behaviors of a synapse at the device level by ionic/electronic devices has shown promising potential in future neural-inspired and compact artificial intelligence systems. To address these issues, this review thoroughly investigates the recent progress in metal-oxide heterostructures for neuromorphic applications. These heterostructures not only offer low power consumption and high stability but also possess optimized electrical characteristics via interface engineering. The paper first outlines various synthesis methods for metal oxides and then summarizes the neuromorphic devices using these materials and their heterostructures. More importantly, we review the emerging multifunctional applications, including neuromorphic vision, touch, and pain systems. Finally, we summarize the future prospects of neuromorphic devices with metal-oxide heterostructures and list the current challenges while offering potential solutions. This review provides insights into the design and construction of metal-oxide devices and their applications for neuromorphic systems. [ABSTRACT FROM AUTHOR]

We fabricated a 12.3 inch panel which was developed for vehicle display. The panel was based on BCE metal oxide structure, through the adjustments of process parameter the TFT device had better stability. We measured both PBTS and NBTS tests under dark environment at Vg = ±30 V and 85 ˚С for 1 hour, the Vth shift in PBTS test is 0.78 V and the Vth shift in NBTS test is 0.08 V. We also delivered a triple‐gate scan driver circuit and by this way we reduced the amount of IC. Mini‐LED backlight combined with Qdyes, the brightness can up to 1000 nits, achieving million level ultra‐high contrast, 100% NTSC and enhancing the sense of image hierarchy. [ABSTRACT FROM AUTHOR]

With the increasing attention to health, especially the impact of COVID-19 in recent years, the research and application of antimicrobial materials have gradually become a research hotspot. Adding antimicrobial agents to various materials is the most common, simple, and effective processing method. The activity of antimicrobial agent has a great influence on the effect and use of antimicrobial material. The photocatalytic metal oxides have the advantages of high antimicrobial performance and long-term activity. In this paper, the antimicrobial mechanisms, types, and applications of photocatalytic metal oxides were described, focusing on the research status and existing problems of photocatalytic metal oxides and doped metal oxides commonly used as inorganic antimicrobials. The future application prospect and research directions of photocatalytic metal oxide antimicrobials were proposed. [ABSTRACT FROM AUTHOR]

In this study, hybrid polymer nanocomposites were produced by combining epoxy (EP) with varying amounts of zirconia (ZrO 2) and yttria (Y2O 3) nanoparticles (NPs), reinforced with multi-walled carbon nanotube (MWCNT) and glass fiber (GF). The objective of this study is to develop and examine the performance of EP nanocomposites through hybridization; for this purpose, hardness and impact tests were conducted in accordance with American Society for Testing and Materials (ASTM) standards. Different sets were produced to investigate the effect of used fillers, including EP/ZrO2, EP/Y2O3, EP/MWCNT, EP/GF, EP/ZrO2/Y2O3, EP/MWCNT/ZrO2/Y2O3, and EP/MWCNT/GF/ZrO2/Y2O3. All findings were compared with the net EP sample. The results showed that the EP nanocomposite samples with low NPs content exhibit much higher mechanical performance than net EP. Furthermore, the additions of MWCNT and GF separately at 0.1 and 0.06 wt.% have increased the impact strength, respectively, to 165.2% and 338.8%, compared with pure EP. As a result, the presence of MWCNTs and GF in the EP-based nanocomposite matrix could make the product both stronger and tougher. [ABSTRACT FROM AUTHOR]

Cement-based materials with thermoelectric effect can realize the conversion of waste heat in building environment, which is of great significance in energy conversion and utilization, and has become a research hotspot in recent years. In this study, three kinds of metal oxides were added into the phase change modified expanded graphite cement-based composites to investigate the impact of metal oxide content on the thermoelectric characteristics of cement composites. The findings shown that the thermoelectric properties of cement-based materials can be enhanced by the addition of metal oxides. The power factor increased to 3.15 μW·m−1·K−2, 3.60 μW·m−1·K−2, and 2.53 μW·m−1·K−2 after mixing ZnO, CuO, and TiO2. This is because the incorporation of metal oxides introduced a large number of interfaces into the cement, increased carrier scattering, strengthened the Seebeck coefficient of cement, and improved the power factor. This work presented a novel strategy to improving the thermoelectric properties of cement-based materials. [ABSTRACT FROM AUTHOR]

Sodium-modified litho-vanadium glasses containing non-magnetic Aluminium ions of composition 50Li2CO3 - (30-X) Na2 CO3-20V2O5 -xAl2O3 (30 = x = 5) (LNVA) glasses were prepared by melt quenching technique. The density of the glass samples was measured and found to increase with the Aluminium content of the glass matrix. The measured values of refractive index and polaron radius of the glass network show opposite behaviour with an increase of Aluminium content. Through band gap energy and refractive index, Oxide ion polarizability and electronic polarizability were determined by using the Lorentz-Lorenz equation. The value of Oxide ion polarizability and electronic polarizability is found to be decreased with decreasing band gap energy and increasing refractive index. The value of optical basicity was measured using electronic polarizability and is found to be decreased with decreasing inter-nuclear distance. The band gap energy values of the glass network were found to decrease from 3.241 to 2.134 eV. The metallisation criterion of the glass material was calculated and found to decrease with Aluminium content. [ABSTRACT FROM AUTHOR]

We synthesized zinc oxide nanoparticles (ZnO NPs) by meticulously controlling both temperature and reaction times, allowing us to fine-tune their crystalline properties, morphology, and particle dimensions. This analysis confirmed the existence of a mixture of rod and sphere shapes (ZnO-I), including rod-shaped NPs with an average size of 14.8 nm × 5.2 nm and spherical NPs with an average diameter of 5.27 nm. We subsequently incorporated these synthesized ZnO NPs into organic light-emitting diode (OLED) devices for red, green, and blue colors, utilizing them as the electron injection layer through a solution-based process. The green OLED device using ZnO-I exhibited a promising current efficiency of 4.02 cd/A and an external quantum efficiency of 1.47%. [ABSTRACT FROM AUTHOR]

Separation of thorium, uranium, and rare earth elements (REEs) requires selective materials with high capacity, good thermal, chemical and radiation resistance. For this aim, Zr, Si and Ti oxide nanoparticles (NPs) have been prepared using metal alkoxide precursors via hydrothermal method. Polyacrylonitrile (PAN) was used as a supporting material to obtain nanocomposite (NC) beads for the potential use in industrial scale applications. The surface characteristics and morphological properties of nano metal oxide powders and composites were determined. Metal uptake and separation studies of thorium and REEs were carried out from sulfuric acid leach solution of Beylikova ore. [ABSTRACT FROM AUTHOR]

In the last several decades, metal oxide thin films have attracted significant attention for the development of various existing and emerging technological applications, including pH sensors. The mandate for consistent and precise pH sensing techniques has been increasing across various fields, including environmental monitoring, biotechnology, food and agricultural industries, and medical diagnostics. Metal oxide thin films grown using physical vapor deposition (PVD) with precise control over film thickness, composition, and morphology are beneficial for pH sensing applications such as enhancing pH sensitivity and stability, quicker response, repeatability, and compatibility with miniaturization. Various PVD techniques, including sputtering, evaporation, and ion beam deposition, used to fabricate thin films for tailoring materials' properties for the advanced design and development of high-performing pH sensors, have been explored worldwide by many research groups. In addition, various thin film materials have also been investigated, including metal oxides, nitrides, and nanostructured films, to make very robust pH sensing electrodes with higher pH sensing performance. The development of novel materials and structures has enabled higher sensitivity, improved selectivity, and enhanced durability in harsh pH environments. The last decade has witnessed significant advancements in PVD thin films for pH sensing applications. The combination of precise film deposition techniques, novel materials, and surface functionalization strategies has led to improved pH sensing performance, making PVD thin films a promising choice for future pH sensing technologies. [ABSTRACT FROM AUTHOR]

By supporting platinum (Pt) and cadmium sulfide (CdS) nanoparticles on indium oxide (In2O3), we fabricated a CdS/Pt/In2O3 photocatalyst. Selective photoreduction of carbon dioxide (CO2) to methane (CH4) was achieved on CdS/Pt/In2O3 with electronic Pt−In2O3 interactions, with CH4 selectivity reaching to 100 %, which is higher than that on CdS/Pt/In2O3 without electronic Pt−In2O3 interactions (71.7 %). Moreover, the enhancement effect of electronic Pt‐(metal‐oxide) interactions on selective photoreduction of CO2 to CH4 also occurs by using other common metal oxides, such as photocatalyst supports, including titanium oxide, gallium oxide, zinc oxide, and tungsten oxide. The electronic Pt‐(metal‐oxide) interactions separate photogenerated electron‐hole pairs and convert CO2 into CO2δ−, which can be easily hydrogenated into CH4 via a CO2δ−→HCOO*→HCO*→CH*→CH4 path, thus boosting selective photoreduction of CO2 to CH4. This offers a new way to achieve selective photoreduction of CO2. [ABSTRACT FROM AUTHOR]

By supporting platinum (Pt) and cadmium sulfide (CdS) nanoparticles on indium oxide (In2O3), we fabricated a CdS/Pt/In2O3 photocatalyst. Selective photoreduction of carbon dioxide (CO2) to methane (CH4) was achieved on CdS/Pt/In2O3 with electronic Pt−In2O3 interactions, with CH4 selectivity reaching to 100 %, which is higher than that on CdS/Pt/In2O3 without electronic Pt−In2O3 interactions (71.7 %). Moreover, the enhancement effect of electronic Pt‐(metal‐oxide) interactions on selective photoreduction of CO2 to CH4 also occurs by using other common metal oxides, such as photocatalyst supports, including titanium oxide, gallium oxide, zinc oxide, and tungsten oxide. The electronic Pt‐(metal‐oxide) interactions separate photogenerated electron‐hole pairs and convert CO2 into CO2δ−, which can be easily hydrogenated into CH4 via a CO2δ−→HCOO*→HCO*→CH*→CH4 path, thus boosting selective photoreduction of CO2 to CH4. This offers a new way to achieve selective photoreduction of CO2. [ABSTRACT FROM AUTHOR]

By supporting platinum (Pt) and cadmium sulfide (CdS) nanoparticles on indium oxide (In2O3), we fabricated a CdS/Pt/In2O3 photocatalyst. Selective photoreduction of carbon dioxide (CO2) to methane (CH4) was achieved on CdS/Pt/In2O3 with electronic Pt−In2O3 interactions, with CH4 selectivity reaching to 100 %, which is higher than that on CdS/Pt/In2O3 without electronic Pt−In2O3 interactions (71.7 %). Moreover, the enhancement effect of electronic Pt‐(metal‐oxide) interactions on selective photoreduction of CO2 to CH4 also occurs by using other common metal oxides, such as photocatalyst supports, including titanium oxide, gallium oxide, zinc oxide, and tungsten oxide. The electronic Pt‐(metal‐oxide) interactions separate photogenerated electron‐hole pairs and convert CO2 into CO2δ−, which can be easily hydrogenated into CH4 via a CO2δ−→HCOO*→HCO*→CH*→CH4 path, thus boosting selective photoreduction of CO2 to CH4. This offers a new way to achieve selective photoreduction of CO2. [ABSTRACT FROM AUTHOR]

By supporting platinum (Pt) and cadmium sulfide (CdS) nanoparticles on indium oxide (In2O3), we fabricated a CdS/Pt/In2O3 photocatalyst. Selective photoreduction of carbon dioxide (CO2) to methane (CH4) was achieved on CdS/Pt/In2O3 with electronic Pt−In2O3 interactions, with CH4 selectivity reaching to 100 %, which is higher than that on CdS/Pt/In2O3 without electronic Pt−In2O3 interactions (71.7 %). Moreover, the enhancement effect of electronic Pt‐(metal‐oxide) interactions on selective photoreduction of CO2 to CH4 also occurs by using other common metal oxides, such as photocatalyst supports, including titanium oxide, gallium oxide, zinc oxide, and tungsten oxide. The electronic Pt‐(metal‐oxide) interactions separate photogenerated electron‐hole pairs and convert CO2 into CO2δ−, which can be easily hydrogenated into CH4 via a CO2δ−→HCOO*→HCO*→CH*→CH4 path, thus boosting selective photoreduction of CO2 to CH4. This offers a new way to achieve selective photoreduction of CO2. [ABSTRACT FROM AUTHOR]

Metal oxide nanowires (NWs) with a high surface area, ease of fabrication, and precise control over diameter and chemical composition are among the best candidates for the realization of resistive gas sensors. Among the different techniques used for the synthesis of materials with NW morphology, approaches based on the vapor–liquid–solid (VLS) mechanism are very popular due to the ease of synthesis, low price of starting materials, and possibility of branching. In this review article, we discuss the gas-sensing features of metal oxide NWs grown by the VLS mechanism, with emphasis on the growth conditions and sensing mechanism. The growth and sensing performance of SnO2, ZnO, In2O3, NiO, CuO, and WO3 materials with NW morphology are discussed. The effects of the catalyst type, growth temperature, and other variables on the morphology and gas-sensing performance of NWs are discussed. [ABSTRACT FROM AUTHOR]

Metal oxides have attracted attention as catalysts for various reduction and oxidation reactions due to their abundance, inexpensiveness, and the possibility of combining different catalytic sites (e. g., acid‐base, redox, and oxygen vacancy sites). Previous results have demonstrated that metal oxides are promising candidates for the hydrodeoxygenation (HDO) reaction, one of the processes that aim to upgrade biomass‐derived products by reducing their oxygen content. In this work, molybdenum oxide (MoO3) was subjected to the acetone HDO reaction leading to new insights concerning the generation of molybdenum oxycarbides (MoOxCy) on stream and their catalytic properties. The characteristics of the MoOxCy phase depended on the temperature and time on stream, affecting the balance of the different catalytic sites and the final products' distribution. The intrinsic correlation between the active sites – mainly Brønsted/Lewis acid sites (AS) and hydrogenation/hydrogenolysis sites (HS) – and the reaction pathways was discussed in detail. [ABSTRACT FROM AUTHOR]

The improper disposal of toxic and carcinogenic organic substances resulting from the manufacture of dyes, drugs and pesticides can contaminate aquatic environments and potable water resources and cause serious damage to animal and human health and to the ecosystem. In this sense, heterogeneous photocatalysis stand out as one effective and cost-effective water depollution technique. The use of metal oxide nanocomposites (MON), from the mixture of two or more oxides or between these oxides and other functional semiconductor materials, have gained increasing attention from researchers and industrial developers as a potential alternative to produce efficient and environmentally friendly photocatalysts for the remediation of water contamination by organic compounds. Thus, this work presents an updated review of the main advances in the use of metal oxide nanocomposites-based photocatalysts for decontamination of water polluted by these substances. A bibliometric analysis allowed to show the evolution of the importance of this research topic in the literature over the last decade. The results of the study also showed that hierarchical and heterogeneous nanostructures of metal oxides, as well as conducting polymers and carbon materials, currently stand out as the main materials for the synthesis of MON, with better photocatalysis performance in the degradation of dyes, pharmaceuticals and pesticides. [ABSTRACT FROM AUTHOR]