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).
引用
收藏
页码:5195 / 5203
页数:9
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