Multifunctional Ni3S2@NF-based electrocatalysts for efficient and durable electrocatalytic water splitting

被引:4
作者
Xu, Xiaomei [1 ]
Mo, Qiaoling [2 ]
Zheng, Kuangqi [3 ]
Xu, Zhaodi [2 ]
Cai, Hu [1 ]
机构
[1] Nanchang Univ, Sch Chem & Chem Engn, 999 Xuefu Ave, Nanchang 330031, Peoples R China
[2] Nanchang Univ, Ctr Anal & Testing, 235 Nanjing East Rd, Nanchang 330029, Peoples R China
[3] Nanchang Univ, Sch Future Technol, 999 Xue Fu Ave, Nanchang 330031, Peoples R China
关键词
OXYGEN EVOLUTION REACTION; HYDROGEN EVOLUTION; HYDROXIDES; EXCELLENT; STORAGE; CARBON; ROUTE; FILMS;
D O I
10.1039/d3dt02035e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Transition-metal sulfides (TMSs) have indeed drawn dramatic interest as a potential species of electrocatalysts by virtue of their unique structural features. However, their poor stability and inherent activity have impeded their use in electrocatalytic water splitting. Here, we provide a rational design of a hierarchical nanostructured electrocatalyst containing CeOx-decorated NiCo-layered double hydroxide (LDH) coupled with Ni3S2 protrusions formed on a Ni foam (NF). Specifically, the as-prepared electrocatalyst, denoted as Ni2Co1 LDH-CeOx/Ni3S2@NF, presents only 250 and 300 mV overpotential at & PLUSMN;100 mA cm(-2), respectively, along with the Tafel slope values of 92 and 52 mV dec(-1), as well remarkable long-term life for water splitting in an alkaline electrolyte. Based on systematic experiments and theoretical analysis, the superior electrocatalytic property in terms of Ni2Co1 LDH-CeOx/Ni3S2@NF can be imputed to the following reasons: the porous framework of Ni3S2@NF provides a largely surface area and high conductivity; the NiCo LDH nanosheets provide enriched active sites and favorable adsorption ability; the oxygen-vacancy-rich CeOx optimizes the electronic configuration. Overall, these factors work synergistically to expedite the catalytic kinetics of splitting water. Our work concentrates on a rational interface to devise efficient, multifunctional, and serviceable electrocatalysts for future applications.
引用
收藏
页码:12378 / 12389
页数:12
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