Porous and B‐site Substituted Y2[Mn0.2Ru0.8]2O7 Pyrochlore for Boosting Acidic Water Oxidation Activity and Stability DOI Open Access

Zhan Tian,

Xin Yang,

Hongrui Jia

et al.

ChemCatChem, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 7, 2024

Abstract Boosting the reaction stability without sacrificing activity and cost is extremely important but full of challenges for RuO 2 ‐based oxygen evolution catalysts. Herein, porous B‐site substituted Y [Mn 0.2 Ru 0.8 ] O 7 (p‐Y ) pyrochlore toward innovatively synthesized. The formed meso‐/macroporous structure can increase specific surface area corresponding active sites, meanwhile, Mn‐substitution modulate electronic structure, stabilize morphology, reduce dosage species. Interestingly, p‐Y performs 50 h stable operation, significantly outperforming commercial (CM) counterpart with less than life. Furthermore, required overpotential to achieve 10 mA cm −2 only 266 mV, accompanied favorable kinetics catalyst utilization.

Language: Английский

Unraveling the competition between the oxygen and chlorine evolution reactions in seawater electrolysis: Enhancing selectivity for green hydrogen production DOI

Catherine Harvey,

Simon Delacroix, Cédric Tard

et al.

Electrochimica Acta, Journal Year: 2024, Volume and Issue: 497, P. 144534 - 144534

Published: June 6, 2024

Language: Английский

Citations

2

Oxygen-defective ruthenium oxide as an efficient and durable electrocatalyst for acidic oxygen evolution reaction DOI

Jingwei Wang,

Lejuan Cai, Zhipeng Yu

et al.

Journal of Materials Chemistry A, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

Oxygen-defective RuO x nanoparticles are synthesized through a one-step sol–gel process, which show outstanding activity and stability for acidic oxygen evolution reaction at high current densities due to the predominant adsorbate mechanism.

Language: Английский

Citations

2

Engineering Ru‐Au‐Mn Trimetallic Nanostructure for High‐Performance Acidic Oxygen Evolution Electrocatalysis DOI
Yuhang Zhang, Shuai Yue, Rong Cao

et al.

ChemCatChem, Journal Year: 2024, Volume and Issue: 16(21)

Published: July 25, 2024

Abstract Developing highly efficient and stable electrocatalysts in acidic media is essential for proton exchange membrane water electrolyzers (PEMWEs). Especially oxygen evolution reaction (OER), high overpotential needed to overcome the thermodynamic energy barrier of splitting. Herein, we report a high‐efficiency self‐supported ternary alloy OER catalyst with activity good durability electrolytes by simple electrodeposition method. The as‐prepared electrocatalyst consists Ru, Au, Mn which deposited on carbon fiber paper (denoted as RuAuMn‐CFP). RuAuMn‐CFP exhibits superior only requires an 131 mV at 10 mA cm −2 outstanding stability 30 h (10 ) media, outperforms commercial Ru/C Ir/C catalysts. Besides, 140 mV, exhibited remarkable mass 29.63 mA/mg OER. It 7.9 times 23.8 higher than catalysts (3.73 mA/mg, 1.24 respectively).

Language: Английский

Citations

1

Customizing hetero-structured high-entropy alloy/oxide active site by regulating the exsolution strategy for highly efficient water splitting DOI

Yue Deng,

Tingting Wang,

Qingpeng Sun

et al.

Journal of Alloys and Compounds, Journal Year: 2024, Volume and Issue: 1004, P. 175879 - 175879

Published: Aug. 6, 2024

Language: Английский

Citations

1

Porous and B‐site Substituted Y2[Mn0.2Ru0.8]2O7 Pyrochlore for Boosting Acidic Water Oxidation Activity and Stability DOI Open Access

Zhan Tian,

Xin Yang,

Hongrui Jia

et al.

ChemCatChem, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 7, 2024

Abstract Boosting the reaction stability without sacrificing activity and cost is extremely important but full of challenges for RuO 2 ‐based oxygen evolution catalysts. Herein, porous B‐site substituted Y [Mn 0.2 Ru 0.8 ] O 7 (p‐Y ) pyrochlore toward innovatively synthesized. The formed meso‐/macroporous structure can increase specific surface area corresponding active sites, meanwhile, Mn‐substitution modulate electronic structure, stabilize morphology, reduce dosage species. Interestingly, p‐Y performs 50 h stable operation, significantly outperforming commercial (CM) counterpart with less than life. Furthermore, required overpotential to achieve 10 mA cm −2 only 266 mV, accompanied favorable kinetics catalyst utilization.

Language: Английский

Citations

0