Pt3Ti Intermetallic Alloy Formed by Strong Metal-Support Interaction over Pt/TiO2 for the Selective Hydrogenation of Acetophenone

被引:21
|
作者
Zhang, Xixiong [1 ,2 ]
Shi, Wen [2 ]
Li, Yong [2 ]
Zhao, Wenning [2 ]
Han, Shaobo [2 ]
Shen, Wenjie [2 ]
机构
[1] Dalian Univ Technol, Zhang Dayu Sch Chem, Dalian 116024, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
Pt/TiO2; catalysts; strong metal-support interaction; Pt3Ti intermetallic alloy; size dependence; selective hydrogenation; acetophenone; HIGH-TEMPERATURE REDUCTION; PLATINUM NANOPARTICLES; ELECTRON-MICROSCOPY; INITIAL-STAGES; CO OXIDATION; TITANIA; CHEMISORPTION; PARTICLES; CATALYSTS; SURFACE;
D O I
10.1021/acscatal.2c06081
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 strong metal-support interaction over Pt/TiO2 catalysts, which were prepared by depositing size-specified Pt colloids (2-6 nm) onto anatase TiO2 nanosheets dominated by the reactive {001} facets, was featured by the formation of Pt3Ti intermetallic alloy and showed a size-dependent effect. After H-2 reduction at 773 K, bulk Pt-Ti alloys in a mixture of disordered and ordered phases were readily formed over 2 nm Pt particle, while Pt3Ti intermetallic alloys, with a thickness of up to 6 atomic layers, were observed on 4-6 nm Pt particles, showing as a Pt3Ti@Pt core-shell architecture where the Ti atom substituted the Pt atom periodically and interacted with the Pt atom electronically. By further raising the temperature for H-2 reduction to 873 K, the 2-6 nm Pt particles turned into well-crystallized Pt3Ti intermetallic alloys. Both bulk Pt-Ti and Pt3Ti intermetallic alloys suppressed considerably the chemisorption of H-2 and CO but dramatically promoted the selectivity for hydrogenating the C=O bond in acetophenone.
引用
收藏
页码:4030 / 4041
页数:12
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