Deep reconstruction of Ni-doped CoOOH under industrial conditions for efficient oxygen evolution

被引:2
|
作者
Liu, Bin [1 ]
Liu, Xin [1 ]
Wang, Feng-Ge [1 ]
Li, Wen-Jing [1 ]
Xu, Na [1 ]
Zhang, Zhi-Jie [1 ]
Lv, Qian-Xi [1 ]
Chai, Yong-Ming [1 ]
Dong, Bin [1 ]
机构
[1] China Univ Petr East China, Coll Chem & Chem Engn, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxygen evolution reaction; Cobalt molybdate; Cobalt hydroxide; Deep reconstruction; BIFUNCTIONAL ELECTROCATALYSTS; COBALT OXIDES; HYDROXIDE; NANOCUBES; NICKEL;
D O I
10.1016/j.ijhydene.2023.09.079
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
Hydrogen production by water electrolysis is considered to be economical and environmentally friendly. Encouraging the reconstruction of electrocatalysts during the oxygen evolution reaction (OER), which produces a large number of active species with high activity, might be viewed as a promising technique for increased activity. In this work, thermally induced complete reconstructions (TICR) are used to create (oxy)hydroxide with low crystallinity and abundant boundary/vacancy from molybdate precatalysts. The obtained Ni-doped CoOOH (CMO1200-90/NF) with boundary/vacancy demonstrates the efficient electrocatalytic activity for OER. An oxygen precipitation overpotential of 299 mV (100 mA cm-2) is exhibited, while the durability of this structure is verified in a strong corrosive environment (1 M KOH) with a long-term stability of 100 h. Compared with Nidoped CoMoO4 precatalyst, the overpotential is reduced by 102 mV at 100 mA cm-2. During the hydrothermal process, trace amounts of Ni elements are doped and have a synergistic effect with Co to induce the modulation of electronic structure. This work investigates the phenomenon of thermally induced and highlights the commercial potential of deep reconstruction catalysts in high-temperature water electrolysis.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1194 / 1203
页数:10
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