Vacancy-rich heterogeneous MnCo2O4.5@NiS electrocatalyst for highly efficient overall water splitting

被引:1
|
作者
Zhu, Xingxing [1 ]
Ji, Zhengtong [1 ]
Wan, Wubin [2 ]
Zhu, Yongfu [1 ]
Lang, Xingyou [1 ]
Jiang, Qing [1 ]
机构
[1] Jilin Univ, Dept Mat Sci & Engn, Key Lab Automobile Mat, Changchun 130025, Peoples R China
[2] Hubei Univ Automot Technol, Sch Mat Sci & Engn, Shiyan 442002, Peoples R China
基金
中国国家自然科学基金;
关键词
Overall water splitting; Heterojunction engineering; Oxygen vacancies; Spinel oxides; Density functional theory calculation; HYBRID;
D O I
10.1016/j.jcis.2024.09.005
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
Alkaline water electrolysis is regarded as a promising technology for sustainable energy conversion. Spinel oxides have attracted considerable attention as potential catalysts because of their diverse metal valence states. However, achieving the required current densities at low voltages is a challenge due to its limited active sites and suboptimal electron transport. In this study, we present a novel bifunctional catalyst composed of MnCo2O4.5 nanoneedles grown on NiS nanosheets for water electrolysis. Remarkably, MnCo2O4.5@NiS demonstrates exceptional catalytic activity, requiring 187 and 288 mV to achieve a current density of 100 mA cm(- 2) for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. The impressive performance of MnCo2O4.5@NiS is demonstrated by the lower value of voltage 1.44 V needed to deliver the current density of 10 mA cm(- 2,) which outperformed the 1.66 V required for a commercial Pt/C||RuO2 system. Detailed structure analysis and density functional theory (DFT) calculations reveal that the MnCo2O4.5@NiS heterostructure enhances electron transfer at the interface, promotes the formation of oxygen vacancies and tunes the electronic structures of Mn and Co. These findings underscore the potential of MnCo2O4.5@NiS as an efficient and cost-effective electrocatalyst for hydrogen production.
引用
收藏
页码:878 / 884
页数:7
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