Investigating the Influence of Amorphous/Crystalline Interfaces on the Stability of IrO2 for the Oxygen Evolution Reaction in Acidic Electrolyte

被引:5
作者
Ngo , Thi Hong Nga [1 ]
Love, Jonathan [1 ]
O'Mullane, Anthony P. [1 ]
机构
[1] Queensland Univ Technol QUT, Sch Chem & Phys, 2 George St, Brisbane, Qld 4001, Australia
基金
澳大利亚研究理事会;
关键词
Iridium oxide; oxygen evolution reaction; electrodeposition; surface area; annealing; IRIDIUM OXIDE-FILMS; HIGH-SURFACE-AREA; WATER OXIDATION; HIGHLY EFFICIENT; POROUS IRIDIUM; OER ACTIVITY; THIN-FILMS; CATALYST; ELECTROCATALYSTS; NANOPARTICLES;
D O I
10.1002/celc.202300438
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A major challenge with water splitting technology is to develop highly active and stable electrocatalysts for the oxygen evolution reaction (OER). IrO2 - based electrocatalysts are one of the most active electrocatalysts for proton exchange membrane (PEM) electrolysers, due to their excellent activity for the OER in acidic conditions. However, IrO2 often suffers from dissolution during electrolysis due to phase transitions into more soluble forms. Herein, a range of electrodeposited IrO2 films annealed to different temperatures of up to 500degree celsius are prepared to understand the influence that crystalline/amorphous interfaces have on performance during accelerated degradation tests in concentrated acidic solutions. This study showed that an IrO2 film annealed at 300 degree celsius exhibited the highest catalytic activity with a low overpotential of 150 mV at 10 mA cm(-2), the smallest Tafel slope of 51 mV dec(-1), with a less progressive decay in activity over a period of 8 h of accelerated degradation testing. This contrasts with both fully amorphous or more crystalline IrO2 films that decayed much more rapidly within 1 h of testing indicating the role that amorphous/crystalline regions have on OER performance.
引用
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页数:10
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