过电位
氢溢流
氢
铂金
溢出效应
催化作用
化学
制氢
吉布斯自由能
无机化学
电化学
材料科学
物理化学
热力学
电极
有机化学
经济
微观经济学
生物化学
物理
作者
Yumei Feng,Yuhua Xie,Yingjie Yu,Yazhou Chen,Qingting Liu,Haifeng Bao,Fang Luo,Shuyuan Pan,Zehui Yang
标识
DOI:10.1002/anie.202413417
摘要
The substantial promotion of hydrogen evolution reaction (HER) catalytic performance relies on the breakup of the Sabatier principle, which can be achieved by the alternation of the support and electronic metal support interaction (EMSI) is noticed. Due to the utilization of tungsten disulfides as support for platinum (Pt@WS2), surprisingly, Pt@WS2 demands only 31 mV overpotential to attain 10 mA cm‐2 in acidic HER test, corresponding to a 2.5‐fold higher mass activity than benchmarked Pt/C. The pH dependent electrochemical measurements associated with H2‐TPD and in‐situ Raman spectroscopy indicate a hydrogen spillover involved HER mechanism is confirmed. The WS2 support triggers a higher hydrogen binding strength for Pt leading to the increment in hydrogen concentration at Pt sites proved by upshifted d band center as well as lower Gibbs free energy of hydrogen, favourable for hydrogen spillover. Besides, the WS2 shows a comparably lower effect on Gibbs free energy for different Pt layers (‐0.50 eV layer‐1) than carbon black (‐0.88 eV layer‐1) contributing to a better Pt utilization. Also, the theoretical calculation suggests the hydrogen spillover occurs on the 3rd Pt layer in Pt@WS2; moreover, the energy barrier is lowered with increment in hydrogen coverage on Pt.
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