Synergistic Effects in a Nitrogen-Coordinated Zinc Single-Atom Catalyst for Efficient CO2 Cycloaddition

IF 3.9 3区 化学 Q2 CHEMISTRY, PHYSICAL ChemCatChem Pub Date : 2024-12-23 DOI:10.1002/cctc.202401768
Dr. Hushan Chand, Nicolò Allasia, Dr. Luis A. Cipriano, Dr. Giovanni Di Liberto, Prof.Dr. Ik Seon Kwon, Prof.Dr. Min Zhang, Prof.Dr. Gianfranco Pacchioni, Prof.Dr. Venkata Krishnan, Prof.Dr. Gianvito Vilé
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Abstract

The valorization of CO2 into organic carbonates through its cycloaddition to epoxides has garnered significant attention in catalysis. However, the reaction is often hindered by low selectivity, and a key challenge is the development of catalysts capable of effectively activating both CO2 and epoxides simultaneously. In this study, we prepared and characterized a catalyst comprising isolated zinc single atoms dispersed on carbon nitride for the selective CO2 conversion to cyclic carbonates. The monoatomic nature and homogeneous distribution of the zinc species were confirmed utilizing advanced characterization methods, including X-ray absorption spectroscopy and aberration-corrected scanning transmission electron microscopy. The catalyst activity and recyclability were validated through catalytic tests with epichlorohydrin as a model epoxydic compound, and the study scope was subsequently extended to include a wide range of functionalized epoxides. Density functional theory calculations were performed to elucidate the reaction mechanism, revealing that both CO2 and epichlorohydrin interact with the same zinc atom in the cycloaddition process, highlighting the key role of zinc single atoms in promoting the reaction. Overall, the present study provides new insights into the design and optimization of heterogeneous catalysts for CO2 cycloadditions, paving the way for more effective strategies in CO2 valorization and conversion for producing valuable fine chemicals.

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氮配位锌单原子催化剂对CO2高效环加成的协同效应
二氧化碳通过环加成成有机碳酸盐在催化领域引起了极大的关注。然而,该反应往往受到低选择性的阻碍,一个关键的挑战是开发能够同时有效激活CO2和环氧化物的催化剂。在本研究中,我们制备并表征了一种由分散在氮化碳上的孤立锌单原子组成的催化剂,用于选择性地将CO2转化为环状碳酸盐。利用先进的表征方法,包括x射线吸收光谱和像差校正扫描透射电子显微镜,证实了锌的单原子性质和均匀分布。通过以环氧氯丙烷为模型环氧化合物的催化试验,验证了催化剂的活性和可回收性,并将研究范围扩展到广泛的功能化环氧化合物。通过密度泛函理论计算阐明了反应机理,发现CO2和环氧氯丙烷在环加成过程中都与同一个锌原子相互作用,突出了锌单原子在促进反应中的关键作用。总的来说,本研究为CO2环加成的多相催化剂的设计和优化提供了新的见解,为更有效的CO2增值和转化策略铺平了道路,以生产有价值的精细化学品。
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来源期刊
ChemCatChem
ChemCatChem 化学-物理化学
CiteScore
8.10
自引率
4.40%
发文量
511
审稿时长
1.3 months
期刊介绍: With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.
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