Interface Engineering Overall Seawater Splitting of Self-Supporting CeO x @NiCo2O4 Arrays

被引:2
|
作者
Liu, Wenjun [1 ]
Zhao, Junze [2 ]
Dai, Liming [3 ]
Qi, Yanli [1 ]
Liang, Kang [1 ]
Bao, Jian [2 ]
Ren, Yurong [1 ]
机构
[1] Changzhou Univ, Sch Mat Sci & Engn, Changzhou 213164, Peoples R China
[2] Jiangsu Univ, Inst Energy Res, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[3] Nanjing Univ Sci & Technol, Sch Chem & Chem Engn, Nanjing 210094, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
NANOWIRE ARRAYS; EFFICIENT; ELECTROCATALYST; GRAPHENE; HYDROGEN; PHOSPHORUS; CATALYSTS; ELECTRODE; NITRIDE; OXIDE;
D O I
10.1021/acs.inorgchem.4c00303
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
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.
引用
收藏
页码:6016 / 6025
页数:10
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