Co/CoP@NC heterostructures as bifunctional catalysts to enhance the alkaline water splitting

被引:3
|
作者
Liao, Shengxiong [1 ,2 ]
Zhang, Zhijie [1 ,2 ]
Li, Yuying [1 ,2 ]
Zheng, Yuying [1 ,2 ]
Dang, Dai [1 ,2 ]
机构
[1] Jieyang Ctr, Guangdong Prov Lab Chem & Fine Chem Engn, Jieyang 515200, Peoples R China
[2] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China
关键词
Heterostructure; Synergistic effect; Cobalt phosphide; Hydrogen evolution reaction; Oxygen evolution reaction; OXYGEN EVOLUTION REACTION; HYDROGEN; ELECTROCATALYST; COP; EFFICIENT;
D O I
10.1016/j.ijhydene.2024.07.274
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
The development of efficient and stable non-precious bifunctional electrocatalysts is of great significance, but it remains a great challenge. Herein, we have constructed Co/CoP@NC heterojunction catalyst loaded with Co and CoP particles on a nitrogen-doped carbon (NC) substrate using the pyrolysis-oxidation-phosphating strategy. The synergistic effect of Co and CoP particles on the NC substrate increases the active specific surface area, accelerates the charge transfer rate, and improves the intrinsic activities of the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The Co/CoP@NC catalyst exhibits superior HER and OER performance. Specifically, the overpotentials required for Co/CoP@NC to reach the current density of 10 mA cm- 2 are 142 and 186 mV for HER and OER, respectively. This study provides new insights into the design and synthesis of efficient and stable Co-based heterostructure catalysts.
引用
收藏
页码:624 / 631
页数:8
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