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Research Article | Open Access

Carbon-supported CeNCl as an efficient catalyst for CO2 cycloaddition

Li Liu1,2Lingling Zhang2Xiang Chu1,2Baokang Geng1,2Huilin Wang2Zongxiang Li3Xiao Wang1,2 ( )Shuyan Song1,2 ( )Hongjie Zhang1,2,4 ( )
School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei 230026, China
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
Sinocare Incorporation, Changsha 410221, China
Department of Chemistry, Tsinghua University, Beijing 100084, China
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Abstract

The cycloaddition reaction of CO2 with epoxide not only effectively reduces the concentration of CO2 in the atmosphere, but also has excellent industrial application value and up to 100% atom utilization, but there are difficulties in separation and recovery of traditional homogeneous catalysts, harsh reaction conditions of traditional heterogeneous catalysts, and activation of CO2 molecules. In this paper, an easily synthesized heterogeneous catalyst CeNCl/C was used to catalyze the cycloaddition reaction of CO2 with styrene oxide, with a high yield of 92.7%, a high selectivity of 96.7%, a turnover numbers (TON) value of 349, and a good stability demonstrated in six cycle tests (equivalent to 216 h of testing). Through comprehensive studies, it was shown that CeNCl/C contains Lewis acid-base centers as active centers, which can effectively reduce the energy barrier required for ring opening of the reaction substrate, enhance the adsorption and activation of CO2, and promote the formation of intermediates, which led to the acquisition of excellent catalytic activity.

Graphical Abstract

CeNCl/C catalysed the cycloaddition reaction of styrene oxide with CO2 to produce styrene carbonate with a selectivity up to 96.7%, a yield up to 92.7%, a turnover numbers (TON) value of 349 and a stability of more than 90% of the initial activity after six cycles (216 h of catalytic testing). The presence of Lewis acid and Lewis base site in CeNCl/C enhances substrate adsorption and promotes ring-opening of the epoxides, resulting in improved performance.

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Nano Research
Article number: 94907028

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Cite this article:
Liu L, Zhang L, Chu X, et al. Carbon-supported CeNCl as an efficient catalyst for CO2 cycloaddition. Nano Research, 2025, 18(1): 94907028. https://doi.org/10.26599/NR.2025.94907028
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Received: 24 July 2024
Revised: 01 September 2024
Accepted: 10 September 2024
Published: 24 December 2024
© The Author(s) 2025. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).