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Title: Core–shell structured catalysts for thermocatalytic, photocatalytic, and electrocatalytic conversion of CO 2

Abstract

Catalytic conversion of CO2 to produce fuels and chemicals is attractive in prospect because it provides an alternative to fossil feedstocks and the benefit of converting and cycling the greenhouse gas CO2 on a large scale. In today's technology, CO2 is converted into hydrocarbon fuels in Fischer–Tropsch synthesis via the water gas shift reaction, but processes for direct conversion of CO2 to fuels and chemicals such as methane, methanol, and C2+ hydrocarbons or syngas are still far from large-scale applications because of processing challenges that may be best addressed by the discovery of improved catalysts—those with enhanced activity, selectivity, and stability. Core–shell structured catalysts are a relatively new class of nanomaterials that allow a controlled integration of the functions of complementary materials with optimised compositions and morphologies. For CO2 conversion, core–shell catalysts can provide distinctive advantages by addressing challenges such as catalyst sintering and activity loss in CO2 reforming processes, insufficient product selectivity in thermocatalytic CO2 hydrogenation, and low efficiency and selectivity in photocatalytic and electrocatalytic CO2 hydrogenation. In the preceding decade, substantial progress has been made in the synthesis, characterization, and evaluation of core–shell catalysts for such potential applications. Nonetheless, challenges remain in the discovery of inexpensive, robust, regenerablemore » catalysts in this class. This review provides an in-depth assessment of these materials for the thermocatalytic, photocatalytic, and electrocatalytic conversion of CO2 into synthesis gas and valuable hydrocarbons.« less

Authors:
ORCiD logo [1]; ORCiD logo [2]; ORCiD logo [3];  [1];  [1]; ORCiD logo [4]; ORCiD logo [1]
  1. Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore
  2. Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore, Institute of Chemical and Bioengineering, Department of Chemistry and Applied Biosciences
  3. Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering & Technology, Collaborative Innovation Center for Chemical Science & Engineering, Tianjin University, Tianjin
  4. Department of Chemical Engineering, University of California, Davis, USA
Publication Date:
Research Org.:
Univ. of California, Davis, CA (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
OSTI Identifier:
1618782
Alternate Identifier(s):
OSTI ID: 1800146
Grant/Contract Number:  
FG02-04ER15513
Resource Type:
Published Article
Journal Name:
Chemical Society Reviews
Additional Journal Information:
Journal Name: Chemical Society Reviews Journal Volume: 49 Journal Issue: 10; Journal ID: ISSN 0306-0012
Publisher:
Royal Society of Chemistry (RSC)
Country of Publication:
United Kingdom
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY

Citation Formats

Das, Sonali, Pérez-Ramírez, Javier, Gong, Jinlong, Dewangan, Nikita, Hidajat, Kus, Gates, Bruce C., and Kawi, Sibudjing. Core–shell structured catalysts for thermocatalytic, photocatalytic, and electrocatalytic conversion of CO 2. United Kingdom: N. p., 2020. Web. doi:10.1039/C9CS00713J.
Das, Sonali, Pérez-Ramírez, Javier, Gong, Jinlong, Dewangan, Nikita, Hidajat, Kus, Gates, Bruce C., & Kawi, Sibudjing. Core–shell structured catalysts for thermocatalytic, photocatalytic, and electrocatalytic conversion of CO 2. United Kingdom. https://doi.org/10.1039/C9CS00713J
Das, Sonali, Pérez-Ramírez, Javier, Gong, Jinlong, Dewangan, Nikita, Hidajat, Kus, Gates, Bruce C., and Kawi, Sibudjing. Tue . "Core–shell structured catalysts for thermocatalytic, photocatalytic, and electrocatalytic conversion of CO 2". United Kingdom. https://doi.org/10.1039/C9CS00713J.
@article{osti_1618782,
title = {Core–shell structured catalysts for thermocatalytic, photocatalytic, and electrocatalytic conversion of CO 2},
author = {Das, Sonali and Pérez-Ramírez, Javier and Gong, Jinlong and Dewangan, Nikita and Hidajat, Kus and Gates, Bruce C. and Kawi, Sibudjing},
abstractNote = {Catalytic conversion of CO2 to produce fuels and chemicals is attractive in prospect because it provides an alternative to fossil feedstocks and the benefit of converting and cycling the greenhouse gas CO2 on a large scale. In today's technology, CO2 is converted into hydrocarbon fuels in Fischer–Tropsch synthesis via the water gas shift reaction, but processes for direct conversion of CO2 to fuels and chemicals such as methane, methanol, and C2+ hydrocarbons or syngas are still far from large-scale applications because of processing challenges that may be best addressed by the discovery of improved catalysts—those with enhanced activity, selectivity, and stability. Core–shell structured catalysts are a relatively new class of nanomaterials that allow a controlled integration of the functions of complementary materials with optimised compositions and morphologies. For CO2 conversion, core–shell catalysts can provide distinctive advantages by addressing challenges such as catalyst sintering and activity loss in CO2 reforming processes, insufficient product selectivity in thermocatalytic CO2 hydrogenation, and low efficiency and selectivity in photocatalytic and electrocatalytic CO2 hydrogenation. In the preceding decade, substantial progress has been made in the synthesis, characterization, and evaluation of core–shell catalysts for such potential applications. Nonetheless, challenges remain in the discovery of inexpensive, robust, regenerable catalysts in this class. This review provides an in-depth assessment of these materials for the thermocatalytic, photocatalytic, and electrocatalytic conversion of CO2 into synthesis gas and valuable hydrocarbons.},
doi = {10.1039/C9CS00713J},
journal = {Chemical Society Reviews},
number = 10,
volume = 49,
place = {United Kingdom},
year = {Tue May 26 00:00:00 EDT 2020},
month = {Tue May 26 00:00:00 EDT 2020}
}

Journal Article:
Free Publicly Available Full Text
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https://doi.org/10.1039/C9CS00713J

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