Zeolite-encapsulated single-atom catalysts for efficient CO2 conversion
[Display omitted] •Sc,Y,La,Ru,Rh,Ni,Pd,Pt@S-1 catalysts are great candidates for CO2 conversion.•Redox mechanism is preferred by groups 3–9 TM s.•Associative mechanism is preferred by group 10 T Ms.•Groups 11−12 T Ms are predicted to have poor CO2 conversion catalytic activity. Zeolite-supported sin...
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| Published in: | Journal of CO2 utilization Vol. 54; p. 101777 |
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| Main Authors: | , , , , , |
| Format: | Journal Article |
| Language: | English |
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01-12-2021
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| Abstract | [Display omitted]
•Sc,Y,La,Ru,Rh,Ni,Pd,Pt@S-1 catalysts are great candidates for CO2 conversion.•Redox mechanism is preferred by groups 3–9 TM s.•Associative mechanism is preferred by group 10 T Ms.•Groups 11−12 T Ms are predicted to have poor CO2 conversion catalytic activity.
Zeolite-supported single-atom catalysts (SACs) have emerged as a novel class of cheap and tuneable catalysts that can exhibit high activity, selectivity and stability. In this work, we conduct an extensive screening by means of density functional theory calculations to determine the usefulness of 3d, 4d and 5d transition metal (TM) SACs-supported in MFI-type Silicalite-1 zeolite for CO2 conversion. Two reaction mechanisms are considered, namely the redox - direct CO2 dissociation - and associative - hydrogen-assisted CO2 dissociation - mechanisms. Early TM SACs exhibit the lowest energy barriers, which follow the redox mechanism. These energy barriers raise when going right in the periodic table up to group 10, where they become prohibitive and the associative mechanism should dominate. By also considering their resistance to aggregation, we support the use of Sc, Y, La, Ru, Rh, Ni, Pd and Pt as potentially active and stable catalysts for CO2 conversion, given their low energy barriers and strong interaction with the zeolite framework. |
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| AbstractList | [Display omitted]
•Sc,Y,La,Ru,Rh,Ni,Pd,Pt@S-1 catalysts are great candidates for CO2 conversion.•Redox mechanism is preferred by groups 3–9 TM s.•Associative mechanism is preferred by group 10 T Ms.•Groups 11−12 T Ms are predicted to have poor CO2 conversion catalytic activity.
Zeolite-supported single-atom catalysts (SACs) have emerged as a novel class of cheap and tuneable catalysts that can exhibit high activity, selectivity and stability. In this work, we conduct an extensive screening by means of density functional theory calculations to determine the usefulness of 3d, 4d and 5d transition metal (TM) SACs-supported in MFI-type Silicalite-1 zeolite for CO2 conversion. Two reaction mechanisms are considered, namely the redox - direct CO2 dissociation - and associative - hydrogen-assisted CO2 dissociation - mechanisms. Early TM SACs exhibit the lowest energy barriers, which follow the redox mechanism. These energy barriers raise when going right in the periodic table up to group 10, where they become prohibitive and the associative mechanism should dominate. By also considering their resistance to aggregation, we support the use of Sc, Y, La, Ru, Rh, Ni, Pd and Pt as potentially active and stable catalysts for CO2 conversion, given their low energy barriers and strong interaction with the zeolite framework. |
| ArticleNumber | 101777 |
| Author | Prats, Hector Sayós, Ramón López, Estefanía Alonso, Gerard Huarte-Larrañaga, Fermín Gamallo, Pablo |
| Author_xml | – sequence: 1 givenname: Gerard orcidid: 0000-0001-8162-9270 surname: Alonso fullname: Alonso, Gerard organization: Universitat de Barcelona and Institut de Química Teòrica i Computacional (IQTC), C / Martí i Franquès 1, 08028, Barcelona, Spain – sequence: 2 givenname: Estefanía surname: López fullname: López, Estefanía organization: Universitat de Barcelona and Institut de Química Teòrica i Computacional (IQTC), C / Martí i Franquès 1, 08028, Barcelona, Spain – sequence: 3 givenname: Fermín orcidid: 0000-0001-5503-1881 surname: Huarte-Larrañaga fullname: Huarte-Larrañaga, Fermín organization: Universitat de Barcelona and Institut de Química Teòrica i Computacional (IQTC), C / Martí i Franquès 1, 08028, Barcelona, Spain – sequence: 4 givenname: Ramón surname: Sayós fullname: Sayós, Ramón organization: Universitat de Barcelona and Institut de Química Teòrica i Computacional (IQTC), C / Martí i Franquès 1, 08028, Barcelona, Spain – sequence: 5 givenname: Hector orcidid: 0000-0003-4991-253X surname: Prats fullname: Prats, Hector email: h.garcia@ucl.ac.uk organization: Department of Chemical Engineering, University College London, Roberts Building, Torrington Place, London, WC1E 7JE, UK – sequence: 6 givenname: Pablo orcidid: 0000-0002-8531-8063 surname: Gamallo fullname: Gamallo, Pablo email: gamallo@ub.edu organization: Universitat de Barcelona and Institut de Química Teòrica i Computacional (IQTC), C / Martí i Franquès 1, 08028, Barcelona, Spain |
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| Keywords | MFI Heterogeneous catalysis Single-atom catalysts Transition metals Density functional theory CO2 conversion Zeolites |
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•Sc,Y,La,Ru,Rh,Ni,Pd,Pt@S-1 catalysts are great candidates for CO2 conversion.•Redox mechanism is preferred by groups 3–9 TM s.•Associative... |
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| SubjectTerms | CO2 conversion Density functional theory Heterogeneous catalysis MFI Single-atom catalysts Transition metals Zeolites |
| Title | Zeolite-encapsulated single-atom catalysts for efficient CO2 conversion |
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