Facile Synthesis of Co2P Nanoparticles Embedded in N- and P-Doped Mesoporous Carbon Composite as an Efficient Electrocatalyst for Oxygen Evolution Reaction

被引:2
|
作者
Zhu, Ping [1 ]
Zhu, Ziheng [1 ]
Huang, Junxu [1 ]
He, Yuzhou [1 ]
Liu, Sa [1 ]
机构
[1] Jiangsu Normal Univ, Sch Chem & Mat Sci, Jiangsu Key Lab Green Synthet Chem Funct Mat, Xuzhou 221116, Peoples R China
关键词
HYDROGEN EVOLUTION; COBALT PHOSPHIDE; SURFACE RECONSTRUCTION; METAL PHOSPHIDES; WATER; CATALYSTS; NANOSHEETS; NANORODS;
D O I
10.1021/acs.energyfuels.3c02987
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Developing highly efficient and affordable nonprecious metal catalysts is extremely significant to facilitate the electrochemical oxygen evolution reaction (OER). Herein, we constructed an N- and P-doped material decorated with embedded Co2P nanoparticles (termed as Co2P@NPC) by a facile and environmentally friendly method. The composite has abundant mesopores, rich heteroatom-doped species (such as pyridinic N, graphitic N, and P-C), and coupled Co2P nanoparticles. The desirable nanoarchitecture and composition endow the composite with promising catalytic activity for the OER. Interestingly, the electrocatalytic performance can be effectively boosted by surface self-reconstruction from Co2P into Co (oxy)hydroxide active species during the alkaline OER test. Consequently, the as-prepared Co2P@NPC after the electrochemical activation can afford a low delivery operation potential of 1.587 V at 10 mA cm(-2), surpassing that of the commercial RuO2. Furthermore, the Co2P@NPC||Pt/C-based overall water splitting cell can achieve a voltage of as low as 1.580 V at 10 mA cm(-2) and also shows exceptional stability.
引用
收藏
页码:16933 / 16941
页数:9
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