Stabilization of a Mn-Co Oxide During Oxygen Evolution in Alkaline Media

被引:12
|
作者
Villalobos, Javier [1 ]
Morales, Dulce M. [1 ]
Antipin, Denis [1 ]
Schuck, Goetz [2 ]
Golnak, Ronny [3 ]
Xiao, Jie [3 ]
Risch, Marcel [1 ]
机构
[1] Helmholtz Zentrum Berlin Mat & Energie GmbH, Nachwuchsgruppe Gestaltung Sauerstoffentwicklungs, Hahn Meitner Pl 1, D-14109 Berlin, Germany
[2] Helmholtz Zentrum Berlin Mat & Energie GmbH, Abt Struktur & Dynamik Energiematerialien, Hahn Meitner Pl 1, D-14109 Berlin, Germany
[3] Helmholtz Zentrum Berlin Mat & Energie GmbH, Dept Highly Sensit Xray Spect, Albert Einstein Str 15, D-12489 Berlin, Germany
来源
CHEMELECTROCHEM | 2022年 / 9卷 / 13期
基金
欧洲研究理事会;
关键词
Bimetallic oxides; Catalyst activation; Catalyst stability; Cobalt oxides; Oxygen evolution reaction; WATER OXIDATION CATALYSIS; TRANSITION-METAL OXIDES; MANGANESE OXIDE; RATIONAL DESIGN; ELECTROCATALYSTS; STABILITY; SURFACE; REDOX; ELECTRODE; REDUCTION;
D O I
10.1002/celc.202200482
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Improving the stability of electrocatalysts for the oxygen evolution reaction (OER) through materials design has received less attention than improving their catalytic activity. We explored the effects of Mn addition to a cobalt oxide for stabilizing the catalyst by comparing single phase CoOx and (Co0.7Mn0.3)O-x films electrodeposited in alkaline solution. The obtained disordered films were classified as layered oxides using X-ray absorption spectroscopy (XAS). The CoOx films showed a constant decrease in the catalytic activity during cycling, confirmed by oxygen detection, while that of (Co0.7Mn0.3)O-x remained constant within error as measured by electrochemical metrics. These trends were rationalized based on XAS analysis of the metal oxidation states, which were Co2.7+ and Mn3.7+ in the bulk and similar near the surface of (Co0.7Mn0.3)O-x, before and after cycling. Thus, Mn in (Co0.7Mn0.3)O-x successfully stabilized the bulk catalyst material and its surface activity during OER cycling. The development of stabilization approaches is essential to extend the durability of OER catalysts.
引用
收藏
页数:13
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