傅里叶变换红外光谱
傅里叶变换
原位
傅里叶变换光谱学
红外线的
材料科学
催化作用
金属
光谱学
分析化学(期刊)
化学
光学
物理
有机化学
冶金
量子力学
作者
Xuyuan Nie,Guang Li,Delun Chen,Lifei Ji,Jian Yang,Yanxia Jiang,Binwei Zhang,Zidong Wei,Shi‐Gang Sun
标识
DOI:10.1021/acs.jpcc.4c05670
摘要
The surface electron structure of metal catalysts plays a crucial role in their catalytic performance. Nevertheless, developing simple and reliable methods to evaluate this structure remains challenging. Here, we introduce an electrochemical in situ Fourier transform infrared spectroscopy (FTIRS) CO adsorption probe method to study the surface structure of Pt-based alloy catalysts. Combined with high-angle annular dark-field scanning transmission electron microscopy, X-ray photoelectron spectroscopy, and the in situ FTIRS CO-probe method, our study demonstrated that the red/blueshift of COad wavenumbers could be attributed to the modifications in the surface Pt electronic structure, resulting in a shift of the d-band center for Pt. This would enhance the d-π* feedback effect between Pt and CO and result in the redshifts of the CO adsorption peaks. This phenomenon can also be observed in transition metal–nitrogen–carbon catalysts, further proving the universality of the in situ FTIRS CO-probe method.
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