析氧
双功能
分解水
氧化钴
氟化物
钴
材料科学
催化作用
碱性水电解
氧化物
无机化学
制氢
电解
氢
可逆氢电极
化学工程
化学
电化学
冶金
电极
光催化
物理化学
有机化学
工程类
参比电极
电解质
作者
Shuo Wang,Cheng‐Zong Yuan,Yunshan Zheng,Yao Kang,Kwan San Hui,Kaixi Wang,Haixing Gao,Duc Anh Dinh,Young‐Rae Cho,Kwun Nam Hui
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-02-20
卷期号:14 (5): 3616-3626
被引量:3
标识
DOI:10.1021/acscatal.4c00294
摘要
Designing cost-effective and durable bifunctional electrocatalysts with high activity for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is crucial for large-scale hydrogen production through water splitting. However, many electrocatalysts undergo surface or bulk reconstruction, leading to an unstable catalytic activity. In this study, we present a facile N2 plasma strategy to enhance the electrocatalytic activity of cobalt-fluoride-oxide (CoFO, herein NCoFO) nanosheets while maintaining reasonably stable performance. The optimized NCoFO nanosheets grown on carbon cloth through a 60 s N2 plasma treatment (NCoFO/CC-60) exhibit remarkable performance with low overpotentials of 203 mV and 230 mV at 10 mA cm–2 for the HER and the OER, respectively. Density functional theory calculations revealed that the enhanced catalytic performance is attributed to the regulated local electronic configuration resulting from plasma treatment. Furthermore, the assembled alkaline electrolyzer NCoFO/CC-60||NCoFO/CC-60 requires an extremely low voltage of 1.48 V to attain 10 mA cm–2 for over a 150 h operation, which is superior to the values obtained for Pt/C||RuO2 (1.50 V) and CoFO/CC||CoFO/CC (1.55 V).
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