催化作用
析氧
电解质
化学工程
分解水
材料科学
化学
无机化学
氧化态
电导率
纳米技术
氧化还原
电化学
电极
物理化学
有机化学
光催化
工程类
作者
Jun Yu,Zheng Wang,Jian Wang,Wenhua Zhong,Min Ju,Rongming Cai,Chen Qiu,Xia Long,Shihe Yang
出处
期刊:Chemsuschem
[Wiley]
日期:2020-07-17
卷期号:13 (19): 5273-5279
被引量:41
标识
DOI:10.1002/cssc.202001542
摘要
Ceria-based catalysts for the oxygen evolution reaction (OER) have received keen interest in recent years owing to their potential excellent cost performance. However, despite a flurry of research activities, the mechanism on how ceria activates those hybrid catalysts is still puzzling. Herein, by controllably modifying the oxidation state of Ce in ceria, it was revealed that creating Ce3+ species, which are redox-coupled to Ce4+ under OER conditions, could enhance the conductivity and optimize the OH* binding, leading to greatly improved OER activity of the catalysts. More importantly, the ceria-based hybrid catalysts also exhibited excellent long-term stability even when operating at a high current density of 50 mA cm-2 in the strong alkaline electrolyte of 6 m KOH for more than 50 h. This work unveils the underlying role of ceria in improving the activity/stability of ceria-based catalysts and opens the way to design and fabricate ceria-based electrocatalysts for water splitting.
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