Related Experiment Video
Updated: Jun 15, 2025

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
(311) High-Index Facet of CeO2 Effectively Promotes the Synthesis of Dimethyl Carbonate from CO2 and Methanol
Zheng-Lan Bai1,2, Tian-Tian Huang1,3, Lin-Xi Qi1
1State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, Fujian, China.
Abstract:
The conversion of CO2 into dimethyl carbonate (DMC) is a reaction of profound environmental and economic significance and has attracted substantial attention. CeO2 stands as a promising catalyst for this reaction, with previous research mainly focused on its low-index facets. In the absence of any dehydrant, the CeO2 catalysts that merely expose low-index facets achieve a maximum DMC yield of 19.5 mmol·g-1·h-1. Herein, we reveal that the (311) high-index facet of CeO2 exhibits an improved catalytic performance compared to the low-index facets. Strikingly, with the strategic exposure of the (311) facet via a two-step hydrothermal method, the yield of DMC can reach 23.1 mmol·g-1·h-1, representing an improvement of 18.5%. According to the results of in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and density functional theory (DFT) calculations, we propose that the effective active structure on the OVsur-(311) facet of CeO2 is Ce3+-OV-Ce3+-OL. The OVsur-(311) facet exhibits abundant Lewis acid-base sites, as well as a unique arrangement of Ce-O, which allow more and easier adsorption and activation of CO2 and methanol. This work would attract more attention to the influence of the CeO2 high-index facet on the synthesis of DMC from CO2 and methanol.
Related Concept Videos
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Catalysis
Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives
Hydroboration-Oxidation of Alkenes
Oxymercuration-Reduction of Alkenes

