海水
化学
接口(物质)
物理化学
水溶液
吉布斯等温线
海洋学
地质学
作者
Wenjun Liu,Junze Zhao,Liming Dai,Yanli Qi,Kang Liang,Jian Bao,Yurong Ren
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-03-18
卷期号:63 (13): 6016-6025
被引量:3
标识
DOI:10.1021/acs.inorgchem.4c00303
摘要
Exploring advanced electrocatalysts for overall seawater splitting is of great significance for large-scale green hydrogen production in which interface engineering has been considered as an effective strategy to enhance the intrinsic activities of the electrocatalysts. In this work, CeOx-modified NiCo2O4 nanoneedle arrays are designed and constructed in situ grown on Ni foam (NF) through a facile two-step synthesis method. Density functional theory calculations reveal that the strong interaction between CeOx and NiCo2O4 can regulate the electronic states of metal surfaces and optimize the electronic structures of the materials, essentially improving the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) properties. Specifically, in alkaline electrolytes, CeOx@NiCo2O4/NF exhibits superior electrocatalytic activities and stabilities, requiring overpotentials of 238 mV for the OER and 144 mV for the HER to achieve a current density of 10 mA cm–2. When applied to a simulated seawater splitting device, the CeOx@NiCo2O4/NF also maintains a battery voltage of 1.66 V to reach 10 mA cm–2 and exhibits good stability for over 60 h, with high faradic efficiencies (FEs) close to 100% for both the OER and HER.
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