Published: Jan. 1, 2024
Language: Английский
Published: Jan. 1, 2024
Language: Английский
Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 677, P. 221 - 231
Published: Aug. 9, 2024
Language: Английский
Citations
45Advanced Science, Journal Year: 2024, Volume and Issue: 11(21)
Published: April 8, 2024
Abstract Developing non‐precious‐metal electrocatalysts that can operate with a low overpotential at high current density for industrial application is challenging. Heterogeneous bimetallic phosphides have attracted much interest. Despite hydrogen evolution reaction (HER) performance, the ordinary oxygen (OER) performance hinders their practical use. Herein, it shown Fe‐doping reverses and enlarges interfacial electrical field heterojunction, turning H intermediate favorable binding sites HER into O OER. Specifically, self‐supported heterojunction catalysts on nickel foam (CoP@Ni 2 P/NF Fe‐CoP@Fe‐Ni P/NF) are readily synthesized. They only require overpotentials of 266 274 mV to drive large 1000 mA cm −2 ( j ) OER, respectively. Furthermore, water splitting cell equipped these electrodes requires voltage 1.724 V excellent durability, demonstrating potential application. This work offers new insights engineering catalysts.
Language: Английский
Citations
21Journal of Colloid and Interface Science, Journal Year: 2025, Volume and Issue: 687, P. 24 - 35
Published: Feb. 8, 2025
Language: Английский
Citations
13Green Chemistry, Journal Year: 2024, Volume and Issue: 26(18), P. 9569 - 9598
Published: Jan. 1, 2024
A comprehensive overview of the use HEM as a catalyst for HER, OER, and water splitting was provided.
Language: Английский
Citations
5Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown
Published: Oct. 10, 2024
Abstract The intrinsically sluggish sulfur reduction reaction kinetics and serious shuttle effect of soluble lithium polysulfides (LiPSs) severely impede the practical commercialization lithium‐sulfur (Li‐S) batteries. Herein, self‐supported tungsten nitride carbide heterostructures with vanadium doping that are directly grown on carbon cloth substrate (CC@V‐W 2 N/WC 1‐ x ) creatively designed for Li‐S batteries, which can tandemly catalyze liquid–liquid conversion liquid–solid polysulfide intermediate free any interference from polymer binders conductive additives. Noteworthy, rich heterointerfaces beneficial rapid charge transfer, strong chemical adsorption toward LiPSs, massive exposed catalytically active sites, remarkable catalytic activities. Consequently, batteries assembled CC@V‐W /S cathodes exhibit high utilization, superior rate capability, decent long‐term cycling stability. Furthermore, experimental analyses theoretical calculations jointly substantiate V‐W N component is more effective in catalyzing long‐chain while V‐WC benefits favorable Li S deposition kinetics. More importantly, pouch cells also fabricated to demonstrate their feasibility applications. This work not only highlights significance tandem catalysis consecutive LiPSs but provides a feasible avenue developing highly efficient electrocatalysts high‐performance
Language: Английский
Citations
5Coordination Chemistry Reviews, Journal Year: 2024, Volume and Issue: 523, P. 216287 - 216287
Published: Oct. 29, 2024
Language: Английский
Citations
4Inorganic Chemistry Frontiers, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Direct seawater electrolysis technology shows great potential, but chloride ions corrode the electrodes and cause competitive reactions, which limits its application.
Language: Английский
Citations
0Journal of Alloys and Compounds, Journal Year: 2025, Volume and Issue: unknown, P. 179593 - 179593
Published: March 1, 2025
Language: Английский
Citations
0Inorganic Chemistry Communications, Journal Year: 2025, Volume and Issue: unknown, P. 114328 - 114328
Published: March 1, 2025
Language: Английский
Citations
0Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown
Published: March 21, 2025
Abstract Iron (Fe)‐based materials hold great potential as urea oxidation reaction (UOR) catalysts, however, the deactivation of active Fe‐oxyhydroxide (FeOOH) species induced by its dissolution during catalytic process under high current densities is still significant challenge. Herein, cobalt (Co) assembled FeOOH constructed, and formation Iron‐Oxygen‐Cobalt (Fe‐O‐Co) bridging triggers electron transfer from Co to Fe sites. This shuttling induces low valence state sites in FeOOH. Co‐FeOOH catalyst achieves a density 1000 mA cm −2 at voltage merely 1.59 V, showing substantial improvement compared pure (1.97 V). Meanwhile, urea‐assisted anion exchange membrane electrolyzer, after 24 h continuous operation , fluctuation 12.4%, significantly lower than that (49.9%). The situ experiments theoretical calculations demonstrate Fe‐O‐Co endows suppressive Fe‐segregation, fast charge Fe(Co)OOH phase negative‐shifted d‐band center metal sites, boosting UOR stability activity.
Language: Английский
Citations
0