DFT Study on the Complex Reaction Networks in the Conversion of Ethylene to Ethylidyne on Flat and Stepped Pd

被引:56
作者
Andersin, J. [1 ]
Lopez, N. [2 ]
Honkala, K. [1 ,3 ]
机构
[1] Univ Jyvaskyla, Dept Chem, Nanosci Ctr, FIN-40014 Jyvaskyla, Finland
[2] Inst Chem Res Catalonia ICIQ, Tarragona 43007, Spain
[3] Univ Jyvaskyla, Dept Phys, Nanosci Ctr, FIN-40014 Jyvaskyla, Finland
基金
芬兰科学院;
关键词
VINYL-ACETATE SYNTHESIS; IN-SITU; ADSORPTION; HYDROGENATION; PD(111); SURFACE; PALLADIUM; ACETYLENE; CATALYSTS; ETHENE;
D O I
10.1021/jp8100877
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
Adsorption and conversion of ethylene to ethylidyne on flat (111) and stepped Pd surfaces have been studied with the aim to unravel the complex chemistry of small organic molecules on Pd. These processes are crucial to understanding many experimental observations on Pd catalysts involved in selective hydrogenations, steam reforming, polymerization, and several other chemical processes. Our results provide a view on the complex chemistry of olefins on the surface, where several competitive processes take place simultaneously and where a hierarchy among different bond activations can be established. For Pd, the C-H bonds of the olefins are the most labile on the surface, followed by C-C and last isomerization processes. From the picture above not always the most straightforward reaction mechanism is necessarily the one taking place on the surface. Scrambling of H atoms on the organic moieties is the most effective way to generate certain (even long lasting) isomers on the surfaces.
引用
收藏
页码:8278 / 8286
页数:9
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