Fluorine-doped nickel oxyhydroxide as a robust electrocatalyst for oxygen evolution reaction

被引:9
|
作者
Wang, Jiajun [1 ]
Zhang, Lei Alexander [2 ]
Ren, Yanmei [1 ]
Wang, Ping [1 ]
机构
[1] South China Univ Technol, Sch Mat Sci & Engn, Guangzhou 510641, Peoples R China
[2] Carnegie Mellon Univ, Dept Mech Engn, Pittsburgh, PA 15217 USA
关键词
Electrochemical water-splitting; Oxygen evolution reaction; Fluorine-doping; Transition metal oxyhydroxide; Anodic electrooxidation; STRUCTURAL STABILITY; COBALT; CATALYSTS; OXIDE; OXIDATION; BORIDE; CHARGE; IRON;
D O I
10.1016/j.electacta.2022.141475
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Fluorine (F) anion doping has recently emerged as a promising approach for boosting the activity of earth -abundant metal catalysts for the oxygen evolution reaction (OER). But many key questions concerning this new approach remain unanswered, including the nature of F-doping, the mechanistic understanding of F-doping effects as well as the long-term stability of F-doped catalysts. Herein, we report a case study of F-NiOOH/Ni (OH)2/NF catalyst that was fabricated using a simple anodic electrooxidation method in a F-containing alkaline solution. A combination of experimental and computational studies revealed that F anions substitute for OH groups in the NiOOH surface layer and such a substitutional F-doping results in significant improvement of OER activity. In particular, the F-doped catalyst possesses outstanding stability when operated in a F-containing electrolyte. For instance, F-NiOOH/Ni(OH)2/NF showed an overpotential fluctuation of only +/- 4 mV in a 100-h constant current test at 100 mA cm-2 in a 0.01 M KF alkaline solution. Furthermore, our study found that this simple F-doping method is applicable to other transition metal oxide/hydroxide catalysts for boosting OER activity.
引用
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页数:8
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