共 50 条
Ionic liquid-assisted controlled synthesis of multi-site Ni2P as a bifunctional catalyst for electrocatalytic water splitting
被引:1
|作者:
Jia, Liqun
[1
]
Yu, Huanhuan
[1
,2
]
Liu, Jiexia
[2
]
Zhu, Baolin
[1
]
Zhang, Shoumin
[1
,3
]
Tian, Jing
[1
]
Xie, Haijiao
[4
]
Zheng, Wenjun
[1
]
机构:
[1] Nankai Univ, Coll Chem, Tianjin 300071, Peoples R China
[2] Shangrao Normal Univ, Coll Chem & Environm Sci, Shangrao 334001, Peoples R China
[3] Nankai Univ, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
[4] Hangzhou Yanqu Informat Technol Co Ltd, Hangzhou 310003, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Nickel phosphide;
Shape control;
Sacrificial template strategy;
Hydrogen evolution reaction;
Oxygen evolution reaction;
HYDROGEN EVOLUTION REACTION;
NICKEL PHOSPHIDE;
EFFICIENT;
NANOSHEETS;
PERFORMANCE;
D O I:
10.1016/j.ijhydene.2024.09.120
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:
It is crucial to develop effective electrocatalysts with multiple active sites for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in order to promote the advance energy conversion and development of sustainable energy technology. Here, we synthesized hierarchical nanostructured Ni2P on carbon cloth using ionic liquid (IL) assisted sacrificial template strategy through a simple two-step hydrothermal phosphatization process, which served as an electrode for enhancing bifunctional water electrolysis. By changing the content of ionic liquids in the solvent, the morphology of Ni(OH)(2) precursors could be regulated, thereby altering the morphology of Ni2P. Ni2P exhibited remarkable electrocatalytic activity towards HER in acidic electrolytes with an overpotential of 132 mV at a current density of 10 mA cm(-2), as well as OER in alkaline media with the overpotential of 309 mV. The excellent electrocatalytic activity of the Ni2P-2 could be attributed to its hierarchical nanostructure providing abundant active sites, which benefits from the structural end-capping effect of ILs.
引用
收藏
页码:1267 / 1279
页数:13
相关论文