A Comparison of Photodeposited RuOX for Alkaline Water Electrolysis

被引:5
|
作者
Daly, Katelynn M. [1 ,2 ]
Jimenez-Villegas, Santiago [1 ,2 ]
Godwin, Benjamin [1 ,2 ,3 ]
Schoen, Martin A. W. [1 ,2 ]
Calderon, Oliver [1 ,2 ]
Chen, Ning [4 ]
Trudel, Simon [1 ,2 ]
机构
[1] Univ Calgary, Dept Chem, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Inst Quantum Sci & Technol, Calgary, AB T2N 1N4, Canada
[3] Univ Victoria, Dept Chem, Elliott Bldg Room 301,3800 Finnerty Rd, Victoria, BC V8P 5C2, Canada
[4] Canadian Light Source, Hard X ray Microanal Beamline, Saskatoon, SK S7N 2V3, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
ruthenium oxide; amorphous materials; oxygen evolution reaction; low-temperature thin film deposition; in operando X-ray absorption spectroscopy; electrocatalysis; OXYGEN EVOLUTION REACTION; IRIDIUM OXIDE; ELECTROCHEMICAL DISSOLUTION; OXIDATION CATALYSIS; RENEWABLE ENERGY; HIGHLY EFFICIENT; THIN-FILMS; ELECTROCATALYSTS; NANOPARTICLES; STABILITY;
D O I
10.1021/acsaem.2c03339
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The storage of renewable energy is a pressing challenge to overcome in the transition toward a power grid based on plentiful, yet intermittent energy supplies. The renewables-driven electrolysis of water to form hydrogen fuel is an attractive avenue, but requires better oxygen-evolution reaction (OER) catalysts to be feasible at scale. RuO2 is touted as one of the superior OER catalysts but only under acidic conditions; RuO2 electrocatalysts suffer from poor stability under alkaline conditions. In this work, we evaluate three photodeposited RuOx OER electrocatalysts, all prepared via a scalable photodeposition method. Based on electrochemical and spectroscopic studies (X-ray photoelectron spectroscopy and X-ray absorption spectroscopy), our main findings are that nanocrystalline RuOx catalysts outperform their amorphous counterpart and are more stable under alkaline (0.1 M KOH) conditions. This works thus lifts a major hurdle toward the use of RuOx for alkaline water electrolysis.
引用
收藏
页码:1449 / 1458
页数:10
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