Construction of Petal-Like CoO/CoP Heterostructures by Oxygen Vacancy Induced P-doping for Efficient Overall Water Splitting

被引:0
|
作者
Ma, Shihang [1 ]
Zhu, Wenchang [1 ]
Feng, Hongbin [1 ]
机构
[1] Qingdao Univ, Inst Mat Energy & Environm, Sch Mat Sci & Engn, Qingdao 266071, Peoples R China
来源
CHEMISTRYSELECT | 2024年 / 9卷 / 10期
基金
中国国家自然科学基金;
关键词
Heterostructures; Bifunctional electrocatalyst; Oxygen vacancy; P-doped; Overall water splitting; HYDROGEN EVOLUTION REACTION; ELECTROCATALYST; CATALYST; GENERATION; NANOSHEETS; REDUCTION; CO3O4;
D O I
10.1002/slct.202303891
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen energy has become a green, high-efficiency new energy source due to its superior characteristics. Overall water splitting is considered as an effective method for hydrogen production. However, the synthesis of non-noble metal-based robust bi-functional electrocatalysts for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are still challenging. Here, the synthesis of petal-like CoO/CoP heterostructures is reported by an oxygen vacancy induced P-doping strategy. The oxygen defect sites of the defective Co3O4-x easily attract phosphorus atoms to enhance the P-doping process, which induces the formation of a two-dimensional CoO/CoP heterojunction structure. Due to the synergistic effect between CoP and CoO phases in the catalyst, the heterostructures can well drive the hydrogen and oxygen evolution reactions under alkaline conditions, and thus substantially promotes overall water splitting with a relatively low potential 1.64 V at 10 mA cm-2 without decay even after the durability test for 24 h. A petal-like CoO/CoP heterostructures was prepared by an oxygen vacancy induced P-doping strategy. The catalysis shows efficient overall water splitting with a low potential of 1.64 V at 10 mA cm-2 over 24 h continuous operation. image
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页数:6
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