Self-supporting electrocatalyst constructed from in-situ transformation of Co(OH)2 to metal-organic framework to Co/CoP/NC nanosheets for high-current-density water splitting

被引:17
|
作者
Chen, Neng [1 ]
Che, Sai [1 ]
Yuan, Yu [1 ]
Liu, Hongchen [1 ]
Ta, Na [1 ]
Li, Guohua [1 ]
Chen, Feng Jiang [1 ]
Ma, Guang [1 ]
Jiang, Bo [1 ]
Wu, Ni [1 ]
Yu, Weiqi [1 ]
Yang, Fan [1 ]
Li, Yongfeng [1 ]
机构
[1] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
In -situ growth; Transition metal phosphide; Self-supporting electrode; Direct device fabrication; Water splitting; HYDROGEN EVOLUTION; EFFICIENT ELECTROCATALYST; LIGAND ENVIRONMENT; OXYGEN REDUCTION; CARBON NANOTUBES; DOPED COP; PHOSPHIDE; TRANSITION; NETWORK; ZIFS;
D O I
10.1016/j.jcis.2023.04.089
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
Transition metal phosphide (TMP) emerges as a promising electrocatalyst for overall water splitting (OWS). However, conventional TMP materials require exogenous metal ions to participate in coordination reactions, which usually suffer from active site blocking, pronounced intrinsic impedance, and inevitable catalyst shedding at high current density. Herein, a novel in-situ construction strategy has been developed to grow N-doped carbon (NC) enwrapped Co/CoP nanosheets directly onto Co foam (abbreviated as CoF) through a three-step transformation of Co to Co(OH)2 to Co-Metal-Organic Framework (Co-MOF) to Co/CoP/NC. In the entire preparation process, Co metal is only provided by the CoF substrate without external metal sources. Such in-situ construction yields tight contact at the interface of the heterogeneous catalyst, leading to much-reduced impedance and boundary vacancy, while the porous nitrogen-doped carbon backbone further endows the catalyst with the exposure of massive active sites, promotes mass transfer, and possesses high electrical conductivity. The Co/CoP/ NC/CoF requires overpotentials of only 64 mV/263 mV@10 mA cm-2 and 414 mV/481 mV@400 mA cm-2 for
引用
收藏
页码:513 / 524
页数:12
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