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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:28
|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
来源:
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.
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页数:11
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