Synthesis and characterization of supported bimetallic overlayer catalysts

被引:13
|
作者
Latusek, Michael P. [1 ]
Heimerl, Rebecca M. [1 ]
Spigarelli, Brett P. [1 ]
Holles, Joseph H. [1 ]
机构
[1] Michigan Technol Univ, Dept Chem Engn, Houghton, MI 49931 USA
关键词
Pd/Re; Pt/Ni; Hydrogen chemisorption; Hydrogen heat of adsorption; DENSITY-FUNCTIONAL THEORY; CORE-SHELL NANOPARTICLES; ISOSTERIC HEAT; HYDROGEN CHEMISORPTION; PARTICLE-SIZE; SURFACES; REDUCTION; ADSORPTION; ALUMINA; RHENIUM;
D O I
10.1016/j.apcata.2009.01.038
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 directed deposition technique was used to synthesize alumina-supported bimetallic overlayer Pd on Re (Re@Pd) and Pt on Ni (Ni@Pt) catalysts. Computational and single crystal studies have predicted unique adsorption properties for similar overlayer type catalysts compared to the monometallic catalysts. The directed deposition technique combines the use of inhibitors and a surface reaction to produce the desired overlayer structure. The Re@Pd and Ni@Pt catalysts were characterized using hydrogen chemisorption, transmission election microscopy (TEM), and energy dispersive spectroscopy (EDS) to correlate properties with synthesis conditions. H-2 chemisorption indicated the proper synthesis conditions to deposit the overlayer metal on the base metal catalyst particle as desired. When a surface deposition inhibitor was not used, evidence for the formation of isolated particles of the overlayer metal was detected. Re@Pd catalysts showed decreased hydrogen heat of adsorption compared to Pd or Re monometallic catalysts as predicted by the literature. Ni@Pt catalysts demonstrated intermediate H-2 heat of adsorption compared to Pt and Ni. TEM/EDS were used to demonstrate that the overlayer metal was associated with the base metal particles as desired. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 87
页数:9
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