Construction of a CoP/MnP/Cu3P heterojunction for efficient methanol oxidation-assisted seawater splitting

被引:0
|
作者
Liu, Weijia [1 ]
Zhou, Min [2 ]
Zhang, Jingwen [3 ]
Liu, Wenxian [1 ]
Qin, Doudou [1 ,3 ]
Liu, Qian [4 ]
Hu, Guangzhi [5 ]
Liu, Xijun [3 ]
机构
[1] Zhejiang Univ Technol, Coll Mat Sci & Engn, Hangzhou 310014, Peoples R China
[2] Shenzhen Technol Univ, Sino German Coll Intelligent Mfg, Shenzhen 518118, Peoples R China
[3] Guangxi Univ, Sch Resources Environm & Mat, MOE Key Lab New Proc Technol Nonferrous Met & Mat, Guangxi Key Lab Proc Nonferrous Met & Featured Mat, Nanning 530004, Guangxi, Peoples R China
[4] Chengdu Univ, Inst Adv Study, Chengdu 610106, Sichuan, Peoples R China
[5] Yunnan Univ, Inst Ecol Res & Pollut Control Plateau Lakes, Sch Ecol & Environm Sci, Kunming 650504, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Methanol oxidation-assisted direct seawater electrolysis has emerged as a potent technology for efficient hydrogen (H2) production alongside high-value chemicals such as formic acid and formaldehyde. However, the large-scale application of this technology heavily relies on developing highly active and robust bifunctional electrocatalysts for methanol oxidation and hydrogen evolution reactions (MOR/HER). Herein, we report a simple hydrothermal-phosphorylation method to synthesize a heterostructured catalyst on copper foam, comprising CoP, MnP, and Cu3P (CoP/MnP/Cu3P@CF). The synergistic interaction among the heterogeneous components endowed CoP/MnP/Cu3P@CF with excellent MOR, oxygen evolution reaction (OER), and HER performance in alkaline seawater electrolytes. Notably, the MOR-assisted CoP/MnP/Cu3P@CF-based seawater electrolyzer catalyst required only 1.410 V to achieve a current density of 10 mA cm-2, significantly lower than the 1.681 V required for an OER-HER seawater electrolyzer. Additionally, the MOR-assisted electrolyzer exhibits high faradaic efficiency and cycling stability, offering the potential for sustainable energy-efficient H2 production.
引用
收藏
页码:953 / 964
页数:12
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