覆盖层
催化作用
金属
吸附
二氧化钛
纳米颗粒
氧化还原
化学工程
化学稳定性
材料科学
钛
无机化学
化学
纳米技术
物理化学
冶金
有机化学
工程类
作者
Hailian Tang,Yang Su,Bingsen Zhang,Adam F. Lee,Mark A. Isaacs,Karen Wilson,Lin Li,Yuegong Ren,Jiahui Huang,Masatake Haruta,Botao Qiao,Xin Liu,Changzi Jin,Dangsheng Su,Junhu Wang,Tao Zhang
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2017-10-06
卷期号:3 (10)
被引量:411
标识
DOI:10.1126/sciadv.1700231
摘要
Supported metal catalysts play a central role in the modern chemical industry but often exhibit poor on-stream stability. The strong metal–support interaction (SMSI) offers a route to control the structural properties of supported metals and, hence, their reactivity and stability. Conventional wisdom holds that supported Au cannot manifest a classical SMSI, which is characterized by reversible metal encapsulation by the support upon high-temperature redox treatments. We demonstrate a classical SMSI for Au/TiO2, evidenced by suppression of CO adsorption, electron transfer from TiO2 to Au nanoparticles, and gold encapsulation by a TiOx overlayer following high-temperature reduction (reversed by subsequent oxidation), akin to that observed for titania-supported platinum group metals. In the SMSI state, Au/TiO2 exhibits markedly improved stability toward CO oxidation. The SMSI extends to Au supported over other reducible oxides (Fe3O4 and CeO2) and other group IB metals (Cu and Ag) over titania. This discovery highlights the general nature of the classical SMSI and unlocks the development of thermochemically stable IB metal catalysts.
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