Effects of carbon defects on interfacial anchoring of NiFe-LDH for seawater electro-oxidation

被引:18
作者
Xu, Heng [1 ]
Xie, Shi-Jun [2 ]
Lv, Chao [2 ]
Li, Jun-Tao [2 ]
Zhou, Yao [2 ]
Sun, Shi-Gang [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Energy, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
OXYGEN EVOLUTION; PERFORMANCE; CATALYST; WATER; ELECTRODEPOSITION; ELECTROCATALYSTS; ELECTROLYSIS; NANOSHEETS;
D O I
10.1039/d2ta09562a
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
The solid-solid interfacial intimacy between the current collector and electrocatalyst is of profound importance in any electrochemical process. Herein, we report that the carbonaceous current collector with high defect density tends to form interfacial C-O-M covalent bonds with the metal sites of NiFe-LDH nanosheets. Such interfacial oxygen bridges on one hand decrease the ohmic contact impedance between the electrocatalyst and current collector, promoting the surface reconstruction of NiFe-LDH and boosting the electrocatalytic activity for the oxygen evolution reaction, and the electrocatalyst-peeling-off phenomenon caused by the coordinative etching of halide anions during seawater electrooxidation, can also be effectively suppressed, on the other hand. The optimal electrode can work steadily for more than 600 h under 500 mA cm(-2) in alkaline natural seawater, showing significantly improved solid-solid interfacial stability.
引用
收藏
页码:10277 / 10286
页数:10
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