A5100761765- Advanced Photocatalysis Techniques
- Catalytic Processes in Materials Science
- Catalysis and Oxidation Reactions
- Electrocatalysts for Energy Conversion
- Metal-Organic Frameworks: Synthesis and Applications
- Gas Sensing Nanomaterials and Sensors
- Ammonia Synthesis and Nitrogen Reduction
- Ferroelectric and Piezoelectric Materials
- Nanomaterials for catalytic reactions
- TiO2 Photocatalysis and Solar Cells
- Electronic and Structural Properties of Oxides
- Microwave Dielectric Ceramics Synthesis
- Advanced Nanomaterials in Catalysis
- Advanced battery technologies research
- Perovskite Materials and Applications
- Copper-based nanomaterials and applications
- X-ray Diffraction in Crystallography
- Catalysis and Hydrodesulfurization Studies
- Multiferroics and related materials
- Quantum Dots Synthesis And Properties
- Chemical Synthesis and Reactions
- Photorefractive and Nonlinear Optics
- Supercapacitor Materials and Fabrication
- CO2 Reduction Techniques and Catalysts
- Crystallization and Solubility Studies
Fuzhou University
2022-2025
Xi'an University of Science and Technology
2022-2024
Southeast University
2024
Shenzhen University
2023-2024
Chinese Academy of Sciences
2024
Luoyang Normal University
2024
University of Jinan
2020-2024
Inner Mongolia University
2023-2024
University of Science and Technology of China
2024
Changsha University
2023
Morphology plays an important role in the physicochemical properties and catalytic activity of Co<sub>3</sub>O<sub>4</sub> catalysts.
Gaseous CO co-existence could improve catalytic toluene oxidation over Co<sub>3</sub>O<sub>4</sub>-based catalysts, and the reaction mechanism on CO/toluene may be mutually independent in presence of both toluene.
Single-atom catalysts (SACs) are deemed as the ultimate ceiling route to release full potential of metal utilization efficiency, while tougher challenge is optimize microstructure for motivating photocatalytic activity move forward. Here, Pt SACs with Pt–C2N and Pt–N2 configurations synthesized by regulating N vacancy level ultrathin g-C3N4 (UCN). The distinctive configuration has been confirmed X-ray absorption fine spectroscopy. Surprisingly, displays a satisfactory H2 evolution...
Solar-to-chemical energy conversion under weak solar irradiation is generally difficult to meet the heat demand of CO2 reduction. Herein, a new concentrated solar-driven photothermal system coupling dual-metal single-atom catalyst (DSAC) with adjacent Ni-N4 and Fe-N4 pair sites designed for boosting gas-solid reduction H2 O simulated irradiation, even ambient sunlight. As expected, (Ni, Fe)-N-C DSAC exhibits superior catalytic performance CO (86.16 μmol g-1 h-1 ), CH4 (135.35 ) CH3 OH (59.81...
The Pt–CeO<sub>2</sub> catalyst with adsorption sites and oxygen-rich vacancies exhibited outstanding activity towards CO toluene co-oxidation.
A series of Pt/MnO<sub>2</sub> catalysts with different MnO<sub>2</sub> crystal structures (α-, β-, γ- and hollow-MnO<sub>2</sub>) were prepared to elucidate the special role strong metal–support interactions (SMSIs) in total toluene deep oxidation on supported Pt catalysts.
Advanced Co<sub>3</sub>O<sub>4</sub> nanoarray-based monolithic catalysts with a stable structure and morphology can be successfully designed utilized to <italic>in situ</italic> grow on Ni substrates, which were investigated for catalytic CO oxidation.
Abstract Hydrogen (H 2 ) production is a key step in solving the energy crisis future. Electrocatalytic water splitting suffers from sluggish anodic oxygen evolution reaction (OER) kinetics leading to low conversion efficiency. Herein, strategy presented that integrates electrochemical flocculation with cathodic hydrogen 0.5 m Na SO 4 . Iron encapsulated nitrogen‐doped carbon nanotubes array on iron foam (Fe@N‐CNT/IF) employed as an electrode for (HER), and Fe@N‐CNT/IF possesses superior HER...
Ammonia (NH
Advanced integrated nanoarray (NA) catalysts have been designed by growing metal-doped Co<sub>3</sub>O<sub>4</sub> arrays on nickel foam with robust adhesion.