Insights into enhanced activity and durability of hierarchical Fe-doped Ni (OH)2/Ni catalysts for alkaline oxygen evolution reaction: In situ XANES studies

被引:22
|
作者
Lee, Sang-Yeon [1 ]
Oh, Hyun-Jung [1 ]
Kim, MinJoong [2 ]
Cho, Hyun-Seok [2 ]
Lee, Yong-Kul [1 ]
机构
[1] Dankook Univ, Dept Chem Engn, Lab Adv Catalysis Energy & Environm, 152 Jukjeonro, Yongin 16892, South Korea
[2] Korea Inst Energy Res, Hydrogen Res Dept, 152 Gajungro, Daejeon 34129, South Korea
基金
新加坡国家研究基金会;
关键词
NiFe-LDH; NiOOH; Fe-doping; Oxygen evolution reaction (OER); In situ XANES; DOUBLE HYDROXIDE ELECTROCATALYSTS; ELECTRODEPOSITION; DESIGN; FILMS;
D O I
10.1016/j.apcatb.2022.122269
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
Nature of activation and degradation of NiFe layered double hydroxide (NiFe-LDH) and hierarchical Fe-doped Ni (OH)2/Ni has been explored using in situ X-ray absorption near edge structure (XANES) spectroscopy coupled with cyclic voltammetry (CV) in a potential range of 0-0.9 V (vs. Hg/HgO). A series of NiFe-LDH samples have been prepared by electrodeposition with varying Ni/Fe molar ratios from 99:1-16:84. Fe has been doped on Ni (OH)2 and anodized Ni as Fe-Ni(OH)2 and Fe-ANi, respectively. CV and electrochemical impedance spectroscopy (EIS) analysis confirm the degradation of NiFe-LDH due to the redox irreversibility of Ni(OH)2/NiOOH. On the other hand, hierarchical Fe-doped Ni(OH)2/Ni shows not only high activity but also stability in alkaline OER. In situ XANES analysis demonstrated that the phase of Ni is maintained with Ni2+ in Fe-ANi, while the phase of Ni2+ changes to Ni3.6+ in NiFe-LDH, contributing to durable OER performance of Fe-ANi even under potential fluctuations.
引用
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页数:11
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