Lacunary polyoxometalate oriented construction of dispersed Ni3S2 confined in WO3 for electrocatalytic water splitting

被引:11
|
作者
Sun, Fengyue [1 ]
Yue, Changle [1 ]
Wang, Jinjin [1 ]
Liu, Yang [1 ]
Bao, Wenjing [1 ]
Liu, Na [1 ]
Tuo, Yongxiao [2 ]
Lu, Yukun [1 ]
机构
[1] China Univ Petr East China, Coll Chem & Chem Engn, State Key Lab Heavy Oil Proc, 66 West Changjiang Rd, Qingdao 266580, Shandong, Peoples R China
[2] China Univ Petr East China, Coll New Energy, 66 West Changjiang Rd, Qingdao 266580, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Polyoxometalates; Electrocatalysts; {Ni-6} cluster; Lacunary direction; Controlled sulfidation; HYDROGEN-EVOLUTION; EFFICIENT ELECTROCATALYST; NANOPARTICLES; HYBRID; TEMPLATE; GRAPHENE; ARRAYS; FILM;
D O I
10.1016/j.jcis.2023.04.144
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
Manufacturing low-cost, high-performance and earth-rich catalysts for hydrogen evolution (HER) and oxygen evolution reactions (OER) is critical to achieving sustainable green hydrogen production. Herein, we utilize lacunary Keggin-structure [PW9O34](9)-(PW9) as a molecular pre-assembly platform to anchor Ni within a single PW9 molecule by vacancy-directed and nucleophile-induced effects for the uniform dispersion of Ni at the atomic level. The chemical coordination of Ni with PW9 can avoid the aggregation of Ni and favor the exposure of active sites. The Ni3S2 confined by WO3 prepared from controlled sulfidation of Ni6PW9/Nickel Foam (Ni6PW9/NF) exhibited excellent catalytic activity in both 0.5 M H2SO4 and 1 M KOH solutions, which required only 86 mV and 107 mV overpotentials for HER at a current density of 10 mA center dot cm(-2) and 370 mV for OER at 200 mA center dot cm(-2). This is attributed to the good dispersion of Ni at the atomic level induced by trivacant PW9 and the enhanced intrinsic activity by synergistic effect of Ni and W. Therefore, the construction of active phase from the atomic level is insightful to the rational design of dispersed and efficient electrolytic catalysts.
引用
收藏
页码:188 / 199
页数:12
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