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  4. Unveiling the Pivotal Role of Ce Coordination Structures and Their Surface Arrangements in Governing 2-Cyanopyridine Hydrolysis for Direct Dimethyl Carbonate Synthesis from CO2 and Methanol
 
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Unveiling the Pivotal Role of Ce Coordination Structures and Their Surface Arrangements in Governing 2-Cyanopyridine Hydrolysis for Direct Dimethyl Carbonate Synthesis from CO2 and Methanol

Journal
ACS Catalysis
Start Page
16861
End Page
16871
ISSN
21555435
Date Issued
2024-01-01
Author(s)
Tian L.
Liao, Yin-Song
Xiao, Zhanping
Sun, Guohan
JYH PIN CHOU  
Wong, Chun-Yuen
Ho, Johnny C.
Zhao, Yufei
PI-TAI CHOU  
Peng, Yung-Kang
DOI
10.1021/acscatal.4c04639
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/723103
Abstract
The direct synthesis of dimethyl carbonate (DMC) from CO2 and methanol presents a promising alternative to conventional methods that use toxic chemicals, but its yield is limited by equilibrium. Coupling this reaction with 2-cyanopyridine (2-Cp) hydrolysis over CeO2-based catalysts was found to significantly boost the DMC yield by removing water. Our recent study has revealed that methanol is the key species being activated by surface Ce sites to produce DMC. The reactivity of surface methoxy species toward CO2 varies greatly with their configuration, which is determined by the Ce coordination structures. A similar challenge remains in understanding the CeO2 surface feature governing the hydrolysis of 2-Cp to 2-picolinamide (2-PA). Herein, CeO2 nanocrystallites with well-defined (111), (110), and (100) surfaces were used to study the effects of Ce coordination structures and their arrangements in this reaction and coupled DMC synthesis. We found that the synergistic adsorption of 2-Cp via cyano-N and pyridine-N on (111) and (110) surfaces enables nucleophilic addition of lattice oxygen, producing imino-like N with stronger Lewis basicity, which in turn facilitates hydrolysis. The (111) surface outperforms the (110) surface due to its unique Ce coordination structure and arrangement, which allows more 2-Cp activation and easier 2-PA desorption. Notably, the (111)-enclosed octahedral CeO2 used herein outperforms the reported pristine CeO2 catalysts in this coupled reaction. In contrast, this synergistic adsorption/activation does not occur on the (100) surface, leading to low activity. These findings provide insights for designing CeO2-based catalysts for CO2 conversion with alcohols and amines using 2-Cp as a dehydrant. © 2024 American Chemical Society.
Subjects
Ce coordination structure
CeO2
direct dimethyl carbonate synthesis
nitrile hydrolysis
surface atomic arrangement
SDGs

[SDGs]SDG13

Publisher
American Chemical Society
Type
journal article

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