Oxide Research Articles

Interplay of size and magnetic effects in electrocatalytic water oxidation activity of sub-10 nm NiOx supported porous hard-carbons.

This report describes a systematic approach for precise engineering of a catalyst-metal oxide interface through combining complementary approaches of chemical vapor deposition and atomic layer deposition. Specifically, Chemical Vapor Deposition (CVD) fabricated nanostructured hard-carbon framework (NCF) is employed as synergistic support for precise deposition of NiOx particles through Atomic Layer Deposition (ALD). The three variants of NCF-NiOx system (dimensions ranging from 3-12 nm, surface coverage ranging from 0.14% to 2%) achieved exhibit unique electrocatalytic water oxidation activities, that are further strongly influenced by an external magnetic field (Hext). This confluence of size engineering and associated magnetic field effects interplay to produce the largest lowering in Rct at Hext = 200 mT. A comprehensive analysis of electrocatalytic parameters including the Tafel slope and double layer capacitance establishes further insights on co-relation of size effect and magnetic properties to understand the role of nanocarbon supported transition metal oxides in water electrolysis.

A eutectic mixture catalyzed straight forward production of functional carbon from Sargassum tenerrimum for energy storage application

Here, we present a sustainable and scalable approach for synthesizing functionalized nanomaterials directly from an abundant natural seaweed resource coupled with a green eutectic mixture. The study utilized crushed seaweed granules obtained from fresh brown seaweed Sargassum tenerrimum (ST) and a eutectic mixture generated through the complexation of urea and a metal salt, which act as both solvent and catalyst to facilitate the straightforward production of metal oxide functionalized nanomaterials. Subjecting seaweed granules and the eutectic mixture to pyrolysis at temperatures between 700 °C and 900 °C in a nitrogen (N2) atmosphere resulted in the formation of ST-derived carbon (STC) functionalized with β-MnO2. The nanoneedles thus synthesized were examined for their electrochemical properties in both three-electrode and two-electrode configurations, employing 6 M KOH and 1 M Na2SO4 as electrolytes. Within the three-electrode framework, β-MnO2 functionalized STC at 800 °C (MSTC-8) displayed a remarkable specific capacitance, of 685.1 F g−1 in alkaline electrolyte and 308.3 F g−1 in neutral electrolyte at 0.1 A g−1, demonstrating a superior performance compared to MSTC-7 and MSTC-9. Additionally, two-electrode experiments and evaluations of cyclic stability were performed on MSTC-7, MSTC-8, and MSTC-9 symmetric supercapacitors. The fabricated symmetric supercapacitor in Na2SO4 with the operational voltage window up to 1.7 V, achieved a maximum energy density of 45.5 Wh/kg and a power density of 172.66 W kg−1. Moreover, the current investigation highlights the enduring performance of MSTC-8//MSTC-8 symmetric supercapacitor, with a capacitance retention of 95 % and 80 % over 20,000 cycles in KOH and Na2SO4 electrolytes respectively.

Preparation of ZnO@SiO2 composite with controllable sizes and tunable fluorescence via alkali-free strategy

In this paper, we present a simple way to achieve the controllable synthesis of composite ZnO@SiO2 materials. γ-aminopropyltriethoxysilane (APTES) was chosen as the silicon source, and pre-synthesized zinc bromoacetate (ZnBA) was selected the functional metal precursor. By simply regulating the water–ethanol volume ratio, it was possible to simultaneously regulate the sizes of both the composite material and the metal nanoparticles. With an increase in the hydroalcoholic volume ratio from 1:1–3:1, the sizes of the silica materials were increased from 615 to 3020 nm, while the sizes of the ZnO nanoparticles were increased from 3.75 to 6.25 nm. Three ZnO@SiO2 materials with blue, green, and yellow fluorescence were obtained. More importantly, the hydroalcoholic volume ratio and the particle size of the material showed a good linear relationship. In addition, a “rapid nucleation–aggregation growth” mechanism was proposed, and the controlled growth of metal oxide nanoparticles was explored.

ZrO2-CeO2/WO3 heterostructure films prepared by magnetron sputtering for humidity-tolerant triethylamine sensing

Up to now, the development of gas sensors based on metal oxide semiconductors (MOSs) that can detect triethylamine (TEA) under high humidity conditions remains a significant challenge. In this study, we present the ZrO2-CeO2/WO3 (ZCW) heterostructure films for TEA detection under high relative humidity, which were prepared by co-sputtering ZrO2 and CeO2 onto the surface of a WO3 film using the radio frequency magnetron sputtering method. The gas sensors based on the ZCW heterostructure films exhibited outstanding TEA-sensing performance, including high response (18.56–20 ppm), rapid response/recovery rate (1/5 s), excellent selectivity, wide detection range (0.5–500 ppm), outstanding reproducibility and stability, and ideal anti-humidity ability. The excellent TEA-sensing properties of the ZCW heterostructure films should be mainly attributed to their unique surface microstructure, abundant oxygen vacancies, and the formation of heterostructures between ZrO2, CeO2, and WO3. Compared to the WO3 film, both the CeO2/WO3 and ZrO2-CeO2/WO3 films demonstrated highly-enhanced humidity-tolerant performance, which should result from the redox reactions between the Ce3+ and Ce4+ ions. This study provides a general method for preparing the MOSs-based TEA sensors that could work under high humidity condition.

Facile hydrothermal synthesis of a tri-metallic Cu-Mn-Ni oxide-based electrochemical pseudo capacitor.

Transition metal oxide nanocomposites with heterostructures have gained a lot of attention for use in supercapacitors owing to their low cost, high surface area, fast transport of ions and electrons and high specific capacitance due to efficacious interplay between the electrode and the electrolytes. In this study, we fabricated tri-metallic Cu, Mn, Ni(CMNO), bi-metallic Mn, Ni(MNO) and mono-metallic Ni(NO) oxides through a facile hydrothermal route. All the fabricated materials were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and energy dispersive spectroscopy (EDX), and their electrochemical properties were studied using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge-discharge (GCD). The CMNO material showed remarkable electrochemical performance with a specific capacitance of 790.63 F g-1 at a current density of 1 A g-1, surpassing the performance of MNO (438.4 F g-1) and NO (290.82 F g-1). Furthermore, CMNO showed high cycling stability with a retention of 96.7% specific capacitance after 8000 cycles. Based on remarkable and unique properties, the CMNO material is regarded as a promising material for new-generation pseudo-capacitor applications.

Metal oxide transistors 3D integration on low-thermal budget

Metal oxide transistors 3D integration on low-thermal budget

Electrical Responsive Coating with a Multilayered TiO2-SnO2-RuO2 Heterostructure on Ti for Controlling Antibacterial Ability and Improving Osseointegration.

The bacterial infection and poor osseointegration of Ti implants could significantly compromise their applications in bone repair and replacement. Based on the carrier separation ability of the heterojunction and the redox reaction of pseudocapacitive metal oxides, we report an electrically responsive TiO2-SnO2-RuO2 coating with a multilayered heterostructure on a Ti implant. Owing to the band gap structure of the TiO2-SnO2-RuO2 coating, electron carriers are easily enriched at the coating surface, enabling a response to the endogenous electrical stimulation of the bone. With the formation of SnO2-RuO2 pseudocapacitance on the modified surface, the postcharging mode can significantly change the surface chemical state of the coating due to the redox reaction, enhancing the antibacterial ability and osteogenesis-related gene expression of the human bone marrow mesenchymal stem cells. Owing to the attraction for Ca2+, only the negatively postcharged SnO2@RuO2 can promote apatite deposition. The in vivo experiment reveals that the S-SnO2@RuO2-NP could effectively kill the bacteria colonized on the surface and promote osseointegration with the synostosis bonding interface. Thus, negatively charging the electrically responsive coating of TiO2-SnO2-RuO2 is a good strategy to endow modified Ti implants with excellent antibacterial ability and osseointegration.

A novel MTCMOS based 8T2M NVSRAM design for low power applications with high temperature endurance

This research investigates, for the first time, a novel eight-transistor-two-memristor (8T2M) nonvolatile static random access memory (NVSRAM) with 7-nm technology. The key innovation in this design lies in the incorporation of multiple-threshold complementary metal oxide semiconductor (MTCMOS) technology with power gating technique, which enables efficient power management and enhanced performance with low leakage current. The implementation of multiple threshold voltage levels allows for dynamic control of transistor behavior, optimizing power consumption and read/write speeds. As compared to a traditional six-transistor (6T) static random access memory (SRAM) cell, it has been ascertained that there is a 33% enhancement in the read margin and an 18% improvement in the write margin. Moreover, the delay for read, write ‘0’ and write ‘1’ is also minimized by 63.89%, 37.99% and 42.77%. Furthermore, the power attenuation is also reduced for read and write by 63.02% and 81.6%, respectively with respect to a conventional SRAM.

Synthesis of InAl-alloyed Ga2O3 nanowires for self-powered ultraviolet detectors by a CVD method.

Ga2O3 is a kind of wide-band gap semiconductor, which has great potential in deep ultraviolet detection because of its high efficiency and fast response. Doping can improve the photoelectric properties of Ga2O3 materials. In this paper, In and Al elements alloyed Ga2O3 nanowires (InAl-Ga2O3 NWs) were successfully grown on p-GaN using a cost-effective chemical vapor deposition method and a vertical structure. The GaN/InAl-Ga2O3 NWs p-n self-powered wide-gap UV photodetector (PD) was constructed based on sputtered gold film as the bottom and top electrodes, and spin coated with polymethyl methacrylate as the insulating layer in the vertical direction. The GaN/InAl-Ga2O3 UV PD exhibits excellent performances, including an extremely low dark current of 0.015 nA, a maximum photocurrent of about 16 nA at zero-bias voltage under 265 nm illumination, and a light-to-dark current ratio greater than 103. The responsivity is 0.94 mA W-1, the specific detectivity is 9.63 × 109 jones, and the good fast response/attenuation time is 31.2/69.6 ms. The self-powered characteristics are derived from the internal electric field formed between p-type GaN and n-type InAl-Ga2O3 NWs, which is conducive to the rapid separation and transfer of photogenerated carriers. This work provides an innovative mechanism of high-performance metal oxide nanowires for the application of p-n junction photodetectors, which can operate without any external bias.

Eco-Friendly Mycogenic Synthesis of Iron Oxide Nanoparticles Using Volvariella volvacea and Unveiling its Potential as Antibiofilm and Anticancer Agents

Abstract This research explores the eco-friendly creation of functional, biocompatible nanomaterials through green chemistry, utilizing natural extracts over chemicals to produce metal and metal oxide nanoparticles. The study focuses on iron oxide nanoparticles synthesized with Volvariella volvacea (GIONP) and evaluates their physical, chemical, and biological traits, including their anticancer capabilities, against traditionally made IONPs (CIONP). GIONPs, confirmed by UV-visible spectroscopy and dynamic light scattering, showed enhanced stability and consistent size distribution. They also demonstrated smaller sizes via Fe-scanning electron microscopy analysis, and X-ray diffraction and Fourier transform infrared studies verified their crystalline structure and organic functional groups. Notably, GIONPs exhibited strong antioxidant properties, low toxicity to blood cells, promising for intravenous use, and greater antimicrobial and antibiofilm activities against various bacterial strains than CIONPs. The study revealed that both GIONPs and CIONPs exhibit a similar degree of toxicity towards MDA-MB 231 cancer cells. The internalization of GIONPs within these cells was verified through a Prussian blue assay and further supported by the concentration-dependent increase in intracellular iron levels post-treatment. These findings underscore the successful formulation of GIONPs that are not only biocompatible and eco-friendly but also capped with bioactive compounds, highlighting their promising applications in the field of biomedicine.

Enhanced photocatalytic activity of green synthesized zinc oxide nanoparticles using low-cost plant extracts

Developing stable and highly efficient metal oxide photocatalysts remains a significant challenge in managing organic pollutants. In this study, zinc oxide nanoparticles (ZnO NPs) were successfully synthesized using various plant extracts, pomegranate (P.M), beetroot roots (B.S), and seder, along with a chemical process. The produced ZnO NPs were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), ultraviolet–visible spectroscopy (UV–Vis), Field Emission Scanning Electron Microscope (FESEM), High-Resolution Transmission Electron Microscopy (HRTEM), and Surface Area. For all prepared samples, the results indicated that the composition of the plant extract affects several characteristics of the produced particles, such as their photocatalytic properties, energy bandgap (Eg), particle size, and the ratio of the two intensity (0 0 2) and (1 0 0) crystalline planes. The particle size of the produced NPs varies between 20 and 30 nm. To examine NPs' photocatalytic activity in the presence of UV light, Methyl Orange (MO) was utilized. The Eg of ZnO synthesized by the chemical method was 3.16 e. V, whereas it was 2.84, 2.63, and 2.59 for P.M, Seder, and B.S extracts, respectively. The most effective ZnO NPs, synthesized using Beetroots, exhibited a degradation efficiency of 87 ± 0.5% with a kinetic rate constant of 0.007 min−1. The ratio of the two intensity (0 0 2) and (1 0 0) crystalline planes was also examined to determine a specific orientation in (0 0 2) that is linked to the production of oxygen vacancies in ZnO, which enhances their photocatalytic efficiency. Furthermore, the increase in photocatalytic effectiveness can be attributed to the improved light absorption by the inter-band gap states and effective charge transfer.

Geographic variations of aggregate mechanical stability controlled by inorganic cementing agents across the East Asian monsoon region

Soil aggregate mechanical properties are of vital importance for plant growth, tillage and soil erosion, and strongly conditioned by the amount and type of cementing agents that differ with soils. As most research focus at the site scale, how aggregate mechanical stability vary across different types of soils at regional scales and underlying mechanisms remain poorly understood. Herein, seven typical zonal soils in heavy textures with an increased status of soil development were collected under two land uses (arable and forest) and at three pedogenic horizons along the mid-temperate to south-subtropical climatic gradient in the East Asian monsoon region. Aggregate tensile strength (Y), specific rupture energy (Esp) and friability (FI) were measured on air-dried aggregates in a compression test, as well as soil cementing agents related to particle size distribution, organic matter and its components, metal oxides, phyllosilicates and exchangeable cations. Y and Esp were most affected by soil type (F = 37.7 and 21.4, p < 0.001), and less affected by land use and soil horizon (F < 8.2). Y and Esp were overall remarkably larger for temperate moderately (257 ∼ 700 kPa and 40 ∼ 261 J kg−1) than for subtropical highly developed soils (171 ∼ 329 kPa and 22 ∼ 52 J kg−1); FI (0.35 ∼ 1.30) showed no distinct geographic trend. Among soil properties, exchangeable polyvalent cations, crystalline Fe and Al oxides, and vermiculite had much larger and significant explanatory power (R2 = 0.33 ∼ 0.54, p < 0.01) than traditional soil properties (organic matter, soil texture and bulk density) (R2 < 0.25, p > 0.01), suggesting the predominant roles of the inorganic cementing agents in aggregate mechanical stability across soil types. Aggregate mechanical stability was increased by exchangeable polyvalent cations and vermiculite (r = 0.71 ∼ 0.81, p < 0.001), and weakened by crystalline Fe and Al oxides (r = −0.77 ∼ −0.74, p < 0.001). Additionally, mean annual precipitation and temperature were negatively correlated with aggregate mechanical stability (r = −0.80 ∼ −0.76, p < 0.001). This study demonstrates the remarkable geographic variations of aggregate mechanical stability under the influence of climate and highlights the importance of clay mineralogy (mainly swelling clay and crystalline Fe and Al oxides) and exchangeable cations at the regional scale.

Enhanced solar-driven photocatalytic hydrogen production, dye degradation, and supercapacitor functionality using MoS2–TiO2 nanocomposite

In our current study, we've devised a promising method to overcome the limitations of nanostructured titanium dioxide (TiO2) with molybdenum disulfide (MoS2) nanoflowers synthesized through a cost-effective and straightforward solvothermal process. The resulting heterostructures function as highly efficient photocatalysts and supercapacitors. The synthesized MoS2–TiO2 nanocomposite demonstrated exceptional performance in various applications, including efficient hydrogen (H2) evolution, dye degradation, and enhanced supercapacitor performance. The combination of MoS2, a two-dimensional transition metal dichalcogenide, and TiO2, a wide-bandgap metal oxide semiconductor, addresses critical challenges in clean energy, environmental remediation, and energy storage. Photocatalytic studies revealed that the MoS2–TiO2 catalysts exhibited the highest activity for hydrogen production, with a rate of 137.93 μmol h−1 g−1, which is three times greater than that of pure MoS2. Additionally, the MoS2–TiO2 nanocomposite demonstrated superior electrochemical performance, with a specific capacitance of 638 F/g. Electrochemical impedance spectroscopy (EIS) showed that the charge transfer kinetics were comparable, highlighting the positive impact of TiO2 without significantly increasing resistance. The MoS2–TiO2 nanocomposite emerges as a transformative material with multifaceted applications, showcasing its versatility in addressing global challenges related to clean energy and environmental sustainability.

One-step formation of synergistic ZnO/SnO2 composite nanostructures derived from annealing of crystalline ZnSn(OH)6 nanocubes for enhanced catalytic degradation of organic pollutants

Binary metal oxides/hydroxides derived primary metal oxide composites have a pivotal role in diverse applications because of the beneficial interfacial contact, good synergism, high porous nature, and high stability. The current work deals with the derived ZnO/SnO2 composite nanostructures from post-annealing crystalline ZnSn(OH)6 (ZTO-RT) nanocubes, initially synthesized via a single-step hydrothermal synthesis method. First, the pristine ZTO-RT is synthesized @ 180 °C in a hydrothermal autoclave. Further, the transformation of ZTO-RT to ZnO/SnO2 composite nanostructures is performed at two different annealing temperatures of 500 °C (ZTO-DV-500) and 750 °C (ZTO-DV-750) in the vacuum. The respective samples' physical characterization was studied and compared using various analytical techniques. The X-ray diffraction analysis affirms the amorphous nature of ZTO-DV-500 and the poly-crystalline nature of ZTO-DV-750. The nanocube morphologies of the samples are retained even at high-temperature sintering. The existence of metal-oxygen bonds on the surface of the ZnO/SnO2 composite is sustained by X-ray photoelectron spectroscopy. ZTO-DV-750 has larger pores (pore volume - 0.091 cm3 g−1) than the ZTO-DV-500 (0.051 cm3 g−1). In the presence of NaBH4 aqueous solution, the enhanced rhodamine B dye degradations of ZTO-DV-750 are observed. At low RhB concentrations (5 mg L−1), the ZTO-DV-500 and ZTO-DV-750 rate constants are determined to be 0.099 and 0.156 min−1, respectively, while at high concentration (10 mg L−1), these values are 0.043, and 0.091 min−1. Therefore, the ZTO-DV-750 composite has shown potent catalytic activity with NaBH4 over ZTO-DV-500 to decolourise organic dyes.

Origin of the Improved Photoelectrochemical and Photocatalytic Activity in a ZnO-TiO2 Nanohybrid Revealed by Experimental and Density Functional Theory Studies.

Heterojunctions of metal oxides have attracted a great deal of attention as photo (electro) catalysts owing to their excellent photoactivity. While multiple fundamental studies have been dedicated to heteroaggregation, self-assembly of oppositely charged particles to obtain heterojunctions for energy applications has been underexplored. Herein, we report the synthesis of ZnO-TiO2 heterojunctions using the electrostatic self-assembly approach. The synthesized ZnO-TiO2 heterojunctions were characterized by using multiple experimental techniques. Density functional theory calculations were conducted to establish the heterojunction formation mechanism and electronic properties. The ZnO-TiO2 nanohybrid was tested for the photodegradation of rhodamine B dye and water splitting applications. The photocatalytic performance of the ZnO-TiO2 nanohybrid is 3.5 times higher than that of bare ZnO. In addition, the heterostructure exhibited an excellent photocurrent density of 2.4 mA cm-2 at a low onset potential during photoelectrochemical oxygen evolution. The performance improvements are attributed to the formation of the type II heterojunction between ZnO and TiO2, which suppresses carrier recombination and enhances carrier transport, boosting the catalytic activity.

Enhancing photovoltaic applications through precipitating agents in ITO/CIS/CeO2/Al heterojunction solar cell

In this groundbreaking study, we successfully synthesized both cerium oxide and copper indium sulphate nanoparticles via co-precipitation method and the same is spray coated on ITO substrate by Jet Nebulizer Spray Pyrolysis (JNSP) technique. A comprehensive characterization of the structural, morphological and Photo-diode properties was conducted using a range of advanced techniques. X-ray diffraction revealed a superior mono-crystalline cubic fluorite structure with a preferred orientation along the (111) plane, indicating exceptional crystal quality. Scanning electron microscopy and transmission electron microscopy images showed the formation of disk-shaped particles with sharp rounded edges, averaging ∼ 5 nm in size. Fourier transform infrared spectroscopy identified the phonon band envelope of the metal oxide (CeO2) network at 848 cm−1 while photoluminescence spectroscopy revealed blue and blue-green emission in the visible spectrum. Thermogravimetric-differential thermal analysis exhibited a total weight loss of 19.52 % with four distinct exothermic and endothermic peaks. X-ray photoelectron spectroscopy confirmed the presence of Ce and O elements, with a minor amount of carbon absorbed from the atmosphere and revealed the dominant occurrence of Ce4+ and minority occurrence of Ce3+. The maximum power conversion efficiency of 0.23 % was achieved for samples prepared using NH3 precipitant making them highly suitable for photovoltaic applications. This work paves the way for future research in optimizing cerium oxide nanoparticles for high-performance photovoltaic devices potentially leading to breakthroughs in renewable energy harvesting.

Integration of High‐Tc Superconductors with High‐Q‐Factor Oxide Mechanical Resonators

AbstractMicro‐mechanical resonators are building blocks of a variety of applications in basic science and consumer electronics. This device technology is mainly based on well‐established and reproducible silicon‐based fabrication processes with outstanding performances in term of mechanical Q‐factor and sensitivity to external perturbations. Broadening the functionalities of micro‐electro‐mechanical systems (MEMS) by the integration of functional materials is a key step for both applied and fundamental science. However, combining functional materials with silicon‐based devices is challenging. An alternative approach is directly fabricating MEMS based on compounds inherently showing non‐trivial functional properties, such as transition metal oxides. Here, a full‐oxide approach is reported, where a high‐ superconductor YBa2Cu3O7 (YBCO) is integrated with high Q‐factor micro‐bridge resonators made of single‐crystal LaAlO3 (LAO) thin films. LAO resonators are tensile strained, with a stress of about 350 MPa, show a Q‐factor above 200k, and have low roughness. YBCO overlayers are grown ex situ by pulsed laser deposition and YBCO/LAO bridges show zero resistance below 78 K and mechanical properties similar to those of bare LAO resonators. These results open new possibilities toward the development of advanced transducers, such as bolometers or magnetic field detectors, as well as experiments in solid state physics, material science, and quantum opto‐mechanics.

Facile Fabrication of Lilac-Like Multiple Self-Supporting WO3 Nanoneedle Arrays with Cubic/Hexagonal Phase Junctions for Highly Sensitive Ethylene Glycol Gas Sensors.

Metal oxides with nanoarray structures have been demonstrated to be prospective materials for the design of gas sensors with high sensitivity. In this work, the WO3 nanoneedle array structures were synthesized by a one-step hydrothermal method and subsequent calcination. It was demonstrated that the calcination of the sample at 400 °C facilitated the construction of lilac-like multiple self-supporting WO3 arrays, with appropriate c/h-WO3 heterophase junction and highly oriented nanoneedles. Sensors with this structure exhibited the highest sensitivity (2305) to 100 ppm ethylene glycol at 160 °C and outstanding selectivity. The enhanced ethylene glycol gas sensing can be attributed to the abundant transport channels and active sites provided by this unique structure. In addition, the more oxygen adsorption caused by the heterophase junction and the aggregation of reaction medium induced by tip effect are both in favor of the improvement on the gas sensing performance.

Interfacial Engineering of Fluorescent Carbon Dots with Metal Oxides for Real-Time Visualization of Oxygen Vacancy Dynamics.

Oxygen vacancy (Vo), as one of the most common surface defects, significantly influence the physiochemical properties of metal oxides. However, it remains a challenge for existing techniques to visualize the evolution of Vo during redox process due to its heterogeneous distribution, small size, and dynamic nature. Herein, the real-time monitoring of such microscopic interfacial events is reported by advantage of the high-contrast fluorescence response of carbon dots (H-CDs) to Vo. The green emissive H-CDs possess a unique disc-shaped structure and exceptional hydrophilicity, allowing their tight adhesion to the surfaces of Vo-rich MgO by simple mixing. Subsequently, a water involved interfacial reaction occurred between H-CDs and Vo, resulting in gradual quenching of the original green emission and simultaneously emergence of bright red fluorescence. Moreover, the spatiotemporal diffusion dynamics and reaction kinetics are investigated by confocal laser scanning microscopy, revealing the time-dependent reorganization and structural heterogeneity at the interface. The finding provides a new toolbox for in situ imaging of Vo-triggered phenomena at a microscopic level, which will be helpful in promoting the rational design of oxide materials.

Synthesis of Copper–Nickel and Iron–Nickel Alloys by Hydrogen Reduction of Mixtures of Metal Oxide Powders

AbstractThe vast majority of metals production is based on the use of carbon as a reductant and/or a heating fuel. This results in a large amount of carbon dioxide emissions and should be minimized to limit global warming. In this study, powders of copper–nickel alloy and iron–nickel of varying compositions were produced in a single step by reduction of mixtures of Cu2O-NiO and Fe2O3-NiO powders, respectively, using hydrogen as a reductant. Reduction was performed in a horizontal tube furnace at 700 °C for 45 min. All processing was in the solid state and alloys were produced directly from elemental metal oxides. Exhaust gases were analyzed using a gas analyzer to measure the water content to track the progress of the reduction. Reduction was declared complete when the water content in exhaust gases matched the level before hydrogen was introduced. Both copper–nickel and iron–nickel alloys were produced successfully. X-ray diffractometry confirmed the absence of oxides in the product and the presence of solid phases in agreement with the relevant binary phase diagram. Energy-dispersive X-ray spectroscopy in a scanning electron microscope showed macroscopic homogeneity at the expected composition for each powder mixture directly after reduction, with microscopic fluctuations of the order of several mass percent, within the limits of fluctuations observed following typical casting processes. These promising results warrant further investigation to apply this concept to more chemistries and to scale up the process to a pilot scale. Graphical Abstract