High-density defects in ordered macroporous-mesoporous CoNiFe-LDHs for efficient and robust oxygen evolution reaction

被引:16
|
作者
Wang, Ping [1 ]
Song, Shaojia [1 ]
He, Miao [1 ]
Li, Chenyu [1 ]
Wang, Weiwei [1 ]
Li, Huan [1 ]
Yuan, Xilin [1 ]
Fang, Zhao [1 ]
Rinel, Kimaka P. [1 ]
Song, Weiyu [1 ]
Li, Jiang [1 ]
Vlachos, Dionisios G. [2 ,3 ]
Li, Zhenxing [1 ]
机构
[1] China Univ Petr, Coll New Energy & Mat, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[2] Univ Delaware, Dept Chem & Biomol Engn, 221 Acad St, Newark, DE 19716 USA
[3] Univ Delaware, Catalysis Ctr Energy Innovat, 221 Acad St, Newark, DE 19716 USA
来源
CHEM CATALYSIS | 2023年 / 3卷 / 02期
基金
中国国家自然科学基金;
关键词
DOUBLE HYDROXIDE NANOSHEETS; METAL-ORGANIC FRAMEWORK; ACTIVATION; CATALYSTS; HYDROGEN; CO2;
D O I
10.1016/j.checat.2022.100497
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
As a result of the agglomeration of layered double-metal hydrox-ides (LDHs), their electrocatalytic activity of oxygen evolution reac-tion (OER) is usually suppressed. Herein, we propose simple co -pre-cipitation and surface etching for the preparation of ordered macroporous-mesoporous CoNiFe-LDHs with high-density defects. The ordered structure avoids the agglomeration of single-layer nanosheets. Meanwhile, the high-density defects on the nanosheet surface generate abundant metal vacancies and oxygen vacancies, distorting the single-layer nanosheets significantly and altering the electronic properties around the metal (M)-M and M-O bonds, which enhances the adsorption of intermediates and accelerates the rate-controlling reaction step of O*-> OOH*. This new material shows an extremely low overpotential of 197 mV at a current density of 10 mA cm -2 and a surprising stability of over 70 h in alkaline me-dia. This work provides a new synthesis protocol for hierarchical porous LDHs with excellent OER catalytic activity.
引用
收藏
页数:19
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