Highly effective carbon fixation via catalytic conversion of CO2 by an acylamide-containing metal-organic framework

On the way toward a sustainable low-carbon future, in addition to physical capture and permanent underground deposition of anthropogenic emitted CO2, an alternative and very attractive way should be carbon fixation via catalytic chemical conversion of CO2 into value-added chemicals and reusable mate...

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Main Authors: Li, Pei-Zhou, Wang, Xiao-Jun, Liu, Jia, Phang, Hui Shi, Li, Yongxin, Zhao, Yanli
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/137598
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1375982023-02-28T19:46:50Z Highly effective carbon fixation via catalytic conversion of CO2 by an acylamide-containing metal-organic framework Li, Pei-Zhou Wang, Xiao-Jun Liu, Jia Phang, Hui Shi Li, Yongxin Zhao, Yanli School of Physical and Mathematical Sciences Science::Chemistry Metal-organic Frameworks Carbon Fixation On the way toward a sustainable low-carbon future, in addition to physical capture and permanent underground deposition of anthropogenic emitted CO2, an alternative and very attractive way should be carbon fixation via catalytic chemical conversion of CO2 into value-added chemicals and reusable materials. A metal−organic framework (MOF) incorporating accessible nitrogen-rich groups and unsaturated metal sites was successfully constructed via solvothermal assembly of an acylamide containing tetracarboxylate ligand and Cu(II) ions. Characterizations including structural analysis, gas adsorption, and Raman spectral detection were carried out to reveal that the MOF presents not only a high porosity with exposed Lewis acid metal sites but also a high CO2-adsorbing capability. Such inherent structural features make the MOF a highly promising candidate as a heterogeneous catalyst for CO2 chemical conversion, which was confirmed by its high efficiency on the CO2 cycloaddition with small-sized epoxides. Due to the size control of the open porous windows, catalytic activity of the MOF shows a sharp difference between small and large epoxides. Remarkably high efficiency and size selectivity on CO2 catalytic conversion enable the MOF to be an advanced heterogeneous catalyst for carbon fixation. ASTAR (Agency for Sci., Tech. and Research, S’pore) MOE (Min. of Education, S’pore) Accepted version 2020-04-06T02:04:23Z 2020-04-06T02:04:23Z 2017 Journal Article Li, P.-Z., Wang, X.-J., Liu, J., Phang, H. S., Li, Y., & Zhao, Y. (2017). Highly effective carbon fixation via catalytic conversion of CO2 by an acylamide-containing metal-organic framework. Chemistry of Materials, 29, 9256-9261. doi:10.1021/acs.chemmater.7b03183 0897-4756 https://hdl.handle.net/10356/137598 10.1021/acs.chemmater.7b03183 29 9256 9261 en Chemistry of Materials This document is the Accepted Manuscript version of a Published Work that appeared in final form in Chemistry of Materials, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.chemmater.7b03183 application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry
Metal-organic Frameworks
Carbon Fixation
spellingShingle Science::Chemistry
Metal-organic Frameworks
Carbon Fixation
Li, Pei-Zhou
Wang, Xiao-Jun
Liu, Jia
Phang, Hui Shi
Li, Yongxin
Zhao, Yanli
Highly effective carbon fixation via catalytic conversion of CO2 by an acylamide-containing metal-organic framework
description On the way toward a sustainable low-carbon future, in addition to physical capture and permanent underground deposition of anthropogenic emitted CO2, an alternative and very attractive way should be carbon fixation via catalytic chemical conversion of CO2 into value-added chemicals and reusable materials. A metal−organic framework (MOF) incorporating accessible nitrogen-rich groups and unsaturated metal sites was successfully constructed via solvothermal assembly of an acylamide containing tetracarboxylate ligand and Cu(II) ions. Characterizations including structural analysis, gas adsorption, and Raman spectral detection were carried out to reveal that the MOF presents not only a high porosity with exposed Lewis acid metal sites but also a high CO2-adsorbing capability. Such inherent structural features make the MOF a highly promising candidate as a heterogeneous catalyst for CO2 chemical conversion, which was confirmed by its high efficiency on the CO2 cycloaddition with small-sized epoxides. Due to the size control of the open porous windows, catalytic activity of the MOF shows a sharp difference between small and large epoxides. Remarkably high efficiency and size selectivity on CO2 catalytic conversion enable the MOF to be an advanced heterogeneous catalyst for carbon fixation.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Li, Pei-Zhou
Wang, Xiao-Jun
Liu, Jia
Phang, Hui Shi
Li, Yongxin
Zhao, Yanli
format Article
author Li, Pei-Zhou
Wang, Xiao-Jun
Liu, Jia
Phang, Hui Shi
Li, Yongxin
Zhao, Yanli
author_sort Li, Pei-Zhou
title Highly effective carbon fixation via catalytic conversion of CO2 by an acylamide-containing metal-organic framework
title_short Highly effective carbon fixation via catalytic conversion of CO2 by an acylamide-containing metal-organic framework
title_full Highly effective carbon fixation via catalytic conversion of CO2 by an acylamide-containing metal-organic framework
title_fullStr Highly effective carbon fixation via catalytic conversion of CO2 by an acylamide-containing metal-organic framework
title_full_unstemmed Highly effective carbon fixation via catalytic conversion of CO2 by an acylamide-containing metal-organic framework
title_sort highly effective carbon fixation via catalytic conversion of co2 by an acylamide-containing metal-organic framework
publishDate 2020
url https://hdl.handle.net/10356/137598
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