Dimethyl carbonate synthesis from CO2 and methanol over CeO2: elucidating the surface intermediates and oxygen vacancy-assisted reaction mechanism

被引:1
|
作者
Stoian, Dragos [1 ,2 ,5 ]
Sugiyama, Toshiyuki [3 ]
Bansode, Atul [1 ,6 ]
Medina, Francisco [2 ]
van Beek, Wouter [5 ]
Hasegawa, Jun-ya [3 ]
Nakayama, Akira [3 ,4 ]
Urakawa, Atsushi [1 ,6 ]
机构
[1] Barcelona Inst Sci & Technol BIST, Inst Chem Res Catalonia ICIQ, Av Paisos Catalans 16, Tarragona 43007, Spain
[2] Univ Rovira I Virgili, Dept Chem Engn, Ave Paisos Catalans 26, Tarragona 43007, Spain
[3] Hokkaido Univ, Inst Catalysis, Sapporo 0010021, Japan
[4] Univ Tokyo, Dept Chem Syst Engn, Tokyo 1138656, Japan
[5] ESRF European Synchrotron Radiat Facil, Swiss Norwegian Beamlines SNBL, BP 220, F-38043 Grenoble, France
[6] Delft Univ Technol, Dept Chem Engn, Catalysis Engn, Maasweg 9, NL-2629 HZ Delft, Netherlands
基金
日本科学技术振兴机构;
关键词
CATALYTIC-PROPERTIES; ZIRCONIA CATALYSTS; DIOXIDE; CERIA; SPECTROSCOPY; ADSORPTION; EFFICIENT; ALCOHOL; SITES;
D O I
10.1039/d3sc04466a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Surface intermediate species and oxygen vacancy-assisted mechanism over CeO2 catalyst in the direct dimethyl carbonate (DMC) synthesis from carbon dioxide and methanol are suggested by means of transient spectroscopic methodologies in conjunction with multivariate spectral analysis. How the two reactants, i.e. CO2 and methanol, interact with the CeO2 surface and how they form decisive surface intermediates leading to DMC are unraveled by DFT-based molecular dynamics simulation by precise statistical sampling of various configurations of surface states and intermediates. The atomistic simulations and uncovered stability of different intermediate states perfectly explain the unique DMC formation profile experimentally observed upon transient operations, strongly supporting the proposed oxygen vacancy-assisted reaction mechanism.
引用
收藏
页码:13908 / 13914
页数:7
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