Journal
APPLIED SURFACE SCIENCE
Volume 292, Issue -, Pages 117-127Publisher
ELSEVIER
DOI: 10.1016/j.apsusc.2013.11.096
Keywords
Mechanism; Dimethyl carbonate; Methanol; PdCl2-CuCl2; Density functional theory
Categories
Funding
- National Natural Science Foundation of China (NSFC) [20576093, 20876112, 20936003]
- Specialized Research Fund for the Doctoral Program of Higher Education (SRFDP) [20090032110021]
- Program of Introducing Talents of Discipline to Universities [B06006]
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Surface structure of CuCl2-PdCl2 bimetallic catalyst (Wacker-type catalyst) was built employing density functional theory (DFT) calculations, and the reaction mechanism of methanol oxycarbonylation over the CuCl2-PdCl2 surfaces was also investigated. On the CuCl2-PdCl2 surface, the active site for methanol oxidation was confirmed as Cu-Cl-Cu (Pd). Comparing with pure CuCl2 surface, the introduction of Pd atom causes the electron repopulation on the surface and lowers the energy barrier for methanol oxidation, but the number of the active site decreases with the increasing of Pd doping volume. Agreed with previous experimental results, the Pd site is most favorable for the CO insertion, indicated by the lowest activation barrier for the formation of COOCH3 on Pd atom. The lowest energy barrier for the formation of DMC appears when COOCH3 species adsorbed on Pd atom and methoxyl adsorbed on Cu atoms, which is 0.42 eV. Finally, the reconstruction of the unsaturated surface is a spontaneous and exothermic process. Comparing with other surfaces, the rate-limiting step, methanol oxidation, on CuCl2-PdCl2 surface with Pd/Cu = 1:17 has the lowest energy barrier, which is agreed with the experimental observation that PdCl2-CuCl2 catalyst with Pd/Cu=1:20 has the favorable activity. The adsorbed methoxyl will further lower the activation barrier of methanol oxidation, which is agreed with experimental observation that the Wacker-type catalysts have an induction period in the methanol oxidative carbonylation system. (C) 2013 Elsevier B.V. All rights reserved.
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