催化作用
氢溢流
氧气
吸附
X射线光电子能谱
铂金
氧化还原
化学
溢出效应
拉曼光谱
无机化学
材料科学
光化学
物理化学
化学工程
有机化学
经济
微观经济学
工程类
物理
光学
作者
Jianjun Chen,Shangchao Xiong,Haiyan Liu,Jianqiang Shi,Jinxing Mi,Hao Liu,Zhengjun Gong,Laetitia Oliviero,Françoise Maugé,Junhua Li
标识
DOI:10.1038/s41467-023-39226-6
摘要
The spillover of oxygen species is fundamentally important in redox reactions, but the spillover mechanism has been less understood compared to that of hydrogen spillover. Herein Sn is doped into TiO2 to activate low-temperature (<100 °C) reverse oxygen spillover in Pt/TiO2 catalyst, leading to CO oxidation activity much higher than that of most oxide-supported Pt catalysts. A combination of near-ambient-pressure X-ray photoelectron spectroscopy, in situ Raman/Infrared spectroscopies, and ab initio molecular dynamics simulations reveal that the reverse oxygen spillover is triggered by CO adsorption at Pt2+ sites, followed by bond cleavage of Ti-O-Sn moieties nearby and the appearance of Pt4+ species. The O in the catalytically indispensable Pt-O species is energetically more favourable to be originated from Ti-O-Sn. This work clearly depicts the interfacial chemistry of reverse oxygen spillover that is triggered by CO adsorption, and the understanding is helpful for the design of platinum/titania catalysts suitable for reactions of various reactants.
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