Ce-doping induced structure evolution in FeNi-based (oxy)hydroxide for highly efficient oxygen evolution reaction

被引:13
|
作者
Liu, Zhonghu [1 ]
Hu, Junhui [1 ]
Li, Shuo [1 ]
Lu, Cheng [1 ]
Feng, Kun [1 ]
Wang, Shifeng [2 ]
Zhong, Jun [1 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat Lab FUNSOM, Jiangsu Key Lab Adv Negat Carbon Technol, Suzhou 215123, Peoples R China
[2] Univ Portsmouth, Sch Energy & Elect Engn, Portsmouth PO1 3DJ, England
基金
中国国家自然科学基金;
关键词
Oxygen evolution reaction; Ce-doping; Reconstruction; X-ray absorption spectroscopy; Microstructure; METAL-ORGANIC FRAMEWORKS; IN-SITU; ELECTROCATALYSTS; HYDROGEN;
D O I
10.1016/j.apsusc.2023.157590
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
Structure evolution of the catalyst typically plays a key role in determining the catalytic activity in harsh reaction environment. Here we report a doping-reconstruction strategy to prepare catalyst for highly efficient oxygen evolution reaction (OER). Ce-doping has been induced in FeNi metal-organic frameworks (MOFs) to change the microstructure, which can further lead to the in-situ formation of active (oxy)hydroxides. As a result, the obtained Ce-FeNiOOH shows a low overpotential of 196 mV at 10 mA cm-2, with a small Tafel slope of 33.5 mV dec- 1 and a good stability for 100 h. Moreover, by coupling with Pt/C, the two-electrode cell can achieve an excellent performance for overall water splitting with a low voltage of 1.44 V at 10 mA cm-2 (1.59 V at 100 mA cm-2). Synchrotron radiation spectroscopy reveals that Fe-O-Ce microstructure has been created with Ce-doping, which plays a key role for the further transition from MOFs to (oxy)hydroxide during OER.
引用
收藏
页数:7
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