Heterogeneous strategy constructing a built-in electric field: CoP/FeP bifunctional electrode for overall water splitting

被引:32
作者
Zeng, Long [1 ]
An, Lu [1 ]
Zhang, Zhijie [1 ]
Zheng, Jie [1 ]
Chen, Wenxuan [1 ]
Liu, Chao [1 ]
Zheng, Yuying [1 ,2 ]
Dang, Dai [1 ,2 ]
Liu, Zhao-Qing [3 ]
机构
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangdong Prov Key Lab Plant Resources Biorefinery, Guangzhou 510006, Peoples R China
[2] Jieyang Ctr, Guangdong Prov Lab Chem & Fine Chem Engn, Jieyang 515200, Peoples R China
[3] Guangzhou Univ, Sch Chem & Chem Engn, Guangzhou Key Lab Clean Energy & Mat,, Key Lab Water Qual & Conservat Pearl River Delta M, Guangzhou 510006, Peoples R China
关键词
Overall water splitting; Bimetallic metal organic frameworks; Phosphide; Synergistic effect; HYDROGEN; EFFICIENT; CATALYST; FEP;
D O I
10.1016/j.cej.2024.152084
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Development of non-noble bifunctional electrocatalysts for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are of great significance under alkaline electrolytes for overall water splitting. In this work, CoP/FeP has been designed and constructed in situ on carbon fiber paper by using the bimetallic metal organic frameworks (MOFs) synthesis strategy. The heterogeneous CoP/FeP displays excellent catalytic activities in both HER and OER of the fully hydrolyzed semi-reaction. Remarkably, CoP/FeP is applied as the bifunctional electrode in anode and cathode to construct an overall water splitting apparatus, resulting in the low cell voltage and excellent stability. The exceptional electrocatalytic performance may be mainly attributed to the heterogeneous interface, which constructs a built-in electric field to provide electron to Co with electron-rich structure, resulting in the strong adsorption of H and weak adsorption of O2 on Co. This study provides an effective and controllable method for the design of self-supporting bimetal phosphide catalysts.
引用
收藏
页数:9
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