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Selective Conversion of CO(2) into Cyclic Carbonate on Atom Level Catalysts

[Image: see text] The conversion of carbon dioxide (CO(2)) into organic carbonates under ambient temperatures and pressures with high conversion and selectivity still faces a great challenge. The zerovalent atomic catalysts (ACs), featuring accurate structure and valence states, provide a new and ac...

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Autores principales: Zheng, Zhiqiang, Wang, Zhongqiang, Xue, Yurui, He, Feng, Li, Yuliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9888658/
https://www.ncbi.nlm.nih.gov/pubmed/36855393
http://dx.doi.org/10.1021/acsmaterialsau.1c00012
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author Zheng, Zhiqiang
Wang, Zhongqiang
Xue, Yurui
He, Feng
Li, Yuliang
author_facet Zheng, Zhiqiang
Wang, Zhongqiang
Xue, Yurui
He, Feng
Li, Yuliang
author_sort Zheng, Zhiqiang
collection PubMed
description [Image: see text] The conversion of carbon dioxide (CO(2)) into organic carbonates under ambient temperatures and pressures with high conversion and selectivity still faces a great challenge. The zerovalent atomic catalysts (ACs), featuring accurate structure and valence states, provide a new and accurate model system for catalysis. Herein we developed a general preadsorption-reduction strategy to synthesize zerovalent cobalt AC on graphdiyne (Co(0)/GDY). The Co(0)/GDY ACs were used for efficient and selective CO(2) fixation. We were surprised to find that Co(0)/GDY ACs reached nearly 100% conversion at 80 °C and 1 atm in CO(2) fixation and with a significantly high turnover frequency (TOF) of 3024.8 h(–1), which is almost several orders larger than that of benchmarked catalysts. Such high conversion and selectivity represent the advantages of emerging catalysts.
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spelling pubmed-98886582023-02-27 Selective Conversion of CO(2) into Cyclic Carbonate on Atom Level Catalysts Zheng, Zhiqiang Wang, Zhongqiang Xue, Yurui He, Feng Li, Yuliang ACS Mater Au [Image: see text] The conversion of carbon dioxide (CO(2)) into organic carbonates under ambient temperatures and pressures with high conversion and selectivity still faces a great challenge. The zerovalent atomic catalysts (ACs), featuring accurate structure and valence states, provide a new and accurate model system for catalysis. Herein we developed a general preadsorption-reduction strategy to synthesize zerovalent cobalt AC on graphdiyne (Co(0)/GDY). The Co(0)/GDY ACs were used for efficient and selective CO(2) fixation. We were surprised to find that Co(0)/GDY ACs reached nearly 100% conversion at 80 °C and 1 atm in CO(2) fixation and with a significantly high turnover frequency (TOF) of 3024.8 h(–1), which is almost several orders larger than that of benchmarked catalysts. Such high conversion and selectivity represent the advantages of emerging catalysts. American Chemical Society 2021-08-07 /pmc/articles/PMC9888658/ /pubmed/36855393 http://dx.doi.org/10.1021/acsmaterialsau.1c00012 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Zheng, Zhiqiang
Wang, Zhongqiang
Xue, Yurui
He, Feng
Li, Yuliang
Selective Conversion of CO(2) into Cyclic Carbonate on Atom Level Catalysts
title Selective Conversion of CO(2) into Cyclic Carbonate on Atom Level Catalysts
title_full Selective Conversion of CO(2) into Cyclic Carbonate on Atom Level Catalysts
title_fullStr Selective Conversion of CO(2) into Cyclic Carbonate on Atom Level Catalysts
title_full_unstemmed Selective Conversion of CO(2) into Cyclic Carbonate on Atom Level Catalysts
title_short Selective Conversion of CO(2) into Cyclic Carbonate on Atom Level Catalysts
title_sort selective conversion of co(2) into cyclic carbonate on atom level catalysts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9888658/
https://www.ncbi.nlm.nih.gov/pubmed/36855393
http://dx.doi.org/10.1021/acsmaterialsau.1c00012
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