Published: Jan. 1, 2025
Language: Английский
Published: Jan. 1, 2025
Language: Английский
Published: Jan. 1, 2025
Language: Английский
Citations
0Chemical Engineering Journal, Journal Year: 2025, Volume and Issue: unknown, P. 160396 - 160396
Published: Feb. 1, 2025
Language: Английский
Citations
0ACS Sustainable Chemistry & Engineering, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 21, 2025
Anion exchange membrane water electrolyzer (AEMWE) represents a promising sustainable method for large-scale industrial-grade hydrogen manufacturing. However, the sluggish kinetics of bifunctional oxygen/hydrogen evolution reaction (OER/HER) electrocatalysts makes it imperative to develop high-performance anode and cathode materials. Herein, P-doped β-phase NiMoO4 (p-β-NiMoO4) nanorods were first constructed as material HER, then α-phase (p-β-NiMoO4-A) derived by an electrochemical phase transformation mechanism was further applied OER. A series characterizations supported that applying sufficient potential β-NiMoO4 can drive from beta alpha. Compared with directly prepared counterpart, this dynamic results in catalyst tuning atomic configuration environment, modifying electronic state, optimizing *OH adsorption ability. Consequently, assembled two-electrode electrolytic cell system contributes remarkable overall water/seawater splitting capacity outstanding long-term durability even under operating conditions. The AEMWE device ultralow voltage 2.15 V at 2.0 A·cm–2 current density confirms applicability electrocatalysts. This study could provide path realize efficient transition nickel–molybdenum-based materials industrial clean energy conversion.
Language: Английский
Citations
0Inorganic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 25, 2025
Pursuing highly active and stable Ru-based catalysts for the oxygen evolution reaction (OER) under acidic conditions is important in advancing proton exchange membrane (PEM) water electrolyzers. Unfortunately, inadequate stability, especially a large current density of catalysts, still hinders its practical application. Herein, we report La doping strategy that simultaneously enhances both OER activity stability RuO2 media. The introduction into induces tensile strain, which effectively weakens covalency Ru–O bonds. This structural modification significantly inhibits Ru dissolution, thereby substantially enhancing RuO2. Meanwhile, modulates electronic structure optimizes adsorption energy intermediates, electrocatalytic activity. Notably, optimized La0.05-RuO2 electrocatalyst presents an excellent performance 0.5 M H2SO4 electrolyte, delivers low overpotential 190 mV at 10 mA cm–2 sustains 150 h without obvious decay 50 cm–2. More importantly, PEM electrolyzer constructed by using our as anode catalyst, acquires 200 1 A cm–2, highlighting strong potential industrial applications. work sheds new light on designing high-performance toward
Language: Английский
Citations
0Published: Jan. 1, 2025
Language: Английский
Citations
0