析氧
化学
电子转移
电催化剂
异质结
煅烧
电化学
氧气
吸附
催化作用
化学工程
无机化学
光化学
电极
物理化学
光电子学
材料科学
有机化学
工程类
生物化学
作者
Xinpeng Sun,Yu‐Hang Zhang,Yue Xiao,Zhiqiang Li,Lingzhi Wei,Ge Yao,Helin Niu,Fangcai Zheng
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-08-19
卷期号:61 (35): 14140-14147
被引量:18
标识
DOI:10.1021/acs.inorgchem.2c02290
摘要
Constructing the active interface in a heterojunction electrocatalyst is critical for the electron transfer and intermediate adsorption (O*, OH*, and HOO*) in alkaline oxygen evolution reaction (OER) but still remains challenging. Herein, a CeO2/Co4N heterostructure is rationally synthesized through the direct calcination of Ce[Co(CN)6], followed by thermal nitridation. The in situ electrochemically generated CoOOH on the surface of Co4N serves as the active site for the OER, and the coupled CeO2 with oxygen vacancy can optimize the energy barrier of intermediate reactions of the OER, which simultaneously boosts the OER performance. Besides, electrochemical measurement results demonstrate that oxygen vacancies in CeO2 and optimized absorption free energy originating from the electron transfer between CeO2 and CoOOH contribute to enhanced OER kinetics. This work provides new insight into regulating the interface heterostructure to rationally design efficient OER electrocatalysts under alkaline conditions.
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