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Structurally Ordered Pt3Co Nanoparticles Anchored on N-Doped Graphene for Highly Efficient Hydrogen Evolution Reaction
被引:24
|作者:
Lin, Caoxin
[1
]
Huang, Zhiqiao
[1
]
Zhang, Zeyi
[1
]
Zeng, Tang
[1
]
Chen, Runzhe
[1
]
Tan, Yangyang
[1
]
Wu, Wei
[1
]
Mu, Shichun
[2
]
Cheng, Niancai
[1
]
机构:
[1] Fuzhou Univ, Coll Mat Sci & Engn, Fuzhou 350108, Peoples R China
[2] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Platinum and cobalt intermetallic nanoparticle;
Hydrogen evolution;
Pt alloy;
Nitrogen doped graphene;
Density functional theory;
D O I:
10.1021/acssuschemeng.0c06547
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Developing highly efficient catalysts for hydrogen evolution reaction (HER) play a significant role in the large-scale application of electrochemical water splitting. Here, we develop an ultrafine ordered Pt3Co NPs supported on N-doped graphene (NG), which achieves high HER activity with a small overpotential of 13 mV at 10 mA cm(-2). More importantly, at the overpotential of 20 mV, the ordered Pt3Co catalyst (Pt3Co/NG-700) indicates 19.0 and 51.8 times mass activity than that of the disordered Pt3Co catalyst (Pt3Co/NG) and commercialized Pt/C catalyst, respectively. Additionally, the Pt3Co/NG-700 electrocatalyst displays outstanding long-term stability under harsh chronopotentiometry and cycling tests in the acidic media. The theory calculations reveal that the extraordinary HER performance on Pt3Co/NG-700 electrocatalyst originates from the charge redistribution of Pt induced by Co in the structurally ordered Pt3Co intermetallic. The charge redistribution of Pt facilitates the adsorption and dissociation of H* and provides a higher electron transfer and better conductivity, resulting in high HER. Our work opens new opportunities to design noble based alloy catalysts for highly efficient HER.
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页码:16938 / 16945
页数:8
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