Nanoscale hetero-structured Co-Co(OH)2 composite/amorphous carbon core/shell bi-functional electrocatalysts electrochemically evolved from metastable hexagonal-phase cobalt for overall water splitting

被引:9
作者
Lu, Pai [1 ]
Chen, Xuyuan [1 ]
机构
[1] Univ South Eastern Norway, Dept Microsyst, Campus Vestfold,Raveien 215, N-3184 Borre, Norway
关键词
Water splitting; Bi-functional electrocatalyst; Nanocomposite; Cobalt; Cobalt hydroxide; BIFUNCTIONAL CATALYST; EFFICIENT; HYDROGEN; ARRAYS; NANOSHEETS; NICKEL; CO;
D O I
10.1016/j.electacta.2021.138517
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Bi-functional electrocatalysts suited to alkaline water splitting systems are highly pursued, towards the most realistic application enabled by simplified electrolyzer design and cost-effective operation. Herein, a novel nanocomposite Co-Co(OH)(2)/C electrocatalyst with nanoscale hetero-structured metastable hexagonal-phase Co (H-Co) crystallites and Co(OH)(2) crystallites encapsulated by amorphous carbon shells is developed. We employ a mild thermal decomposition route coupled with in-situ carbon deposition performed at 400 degrees C to prepare H-Co/C core/shell structured precursor. In a following controllable electrochemical transformation at room temperature the partial conversion of the metastable H-Co to Co(OH)(2) leads to the mutual embedding of nanoscale crystalline H-Co and Co(OH)(2) confined in the amorphous carbon shells. Taking advantage of the nanowire array morphology, carbon coated core/shell structure, nanoscale size, and the synergistic H-Co and Co(OH)(2) bi-components, an outstanding bi-functional electrocatalytic performance for overall water splitting is attained with proved small overpotentials (93 mV for hydrogen evolution reaction, 264 mV for oxygen evolution reaction at 10 mA cm(-2)). (C) 2021 Elsevier Ltd. All rights reserved.
引用
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页数:8
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