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Experimental and Theoretical Insights into Enhanced Hydrogen Evolution over PtCo Nanoalloys Anchored on a Nitrogen-Doped Carbon Matrix
被引:11
作者:
Guo, Jiangnan
[1
]
Liu, Jinlong
[1
]
Mao, Xichen
[1
]
Chu, Shengqi
[2
]
Zhang, Xinxin
[1
]
Luo, Ziyu
[1
]
Li, Jie
[1
]
Wang, Bowen
[1
]
Jia, Chuankun
[3
]
Qian, Dong
[1
]
机构:
[1] Cent South Univ, Coll Chem & Chem Engn, Changsha 410083, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
[3] Changsha Univ Sci & Technol, Inst Energy Storage Technol, Changsha 410114, Peoples R China
基金:
中国国家自然科学基金;
关键词:
HIGHLY EFFICIENT;
OXYGEN EVOLUTION;
ELECTROCATALYSTS;
NANOPARTICLES;
GRAPHENE;
PERFORMANCE;
CATALYST;
HYBRID;
ARRAYS;
COO;
D O I:
10.1021/acs.jpclett.2c01040
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:
The identification of synergistic effect of Pt-based alloys on hydrogen evolution reaction (HER) requires a combination of experimental studies and theoretical calculations. Here, we present the construction of uniform PtCo nanoparticles grown on N-doped carbon frameworks via pyrolyzing Pt and Co ions adsorbed polyaniline, whereby the nanostructure of the nanoalloys can be effectively tuned by controlling the calcination temperature. As-prepared PtCo@NC-900 shows the optimal HER performance in 0.5 M H2SO4, resulting in a high mass activity of 4.31 A mg(Pt)(-1) and excellent operation durability, which far exceeds that of commercial 20 wt % Pt/C (0.30 A mg(P)(t)(-1)). Density functional theory calculations further reveal that the improved HER activity on PtCo(111) is originated from the strong electronic interaction between Pt and Co with favorable electron transfer, allowing for a more suitable binding strength for hydrogen (i.e., Delta G(*H) = -0.164 eV) compared with that of pristine Pt(111) (-0.287 eV).
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页码:5195 / 5203
页数:9
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