journal article·2024-11-13Open access

Optimizing Materials to Boost the Valorization of CO2: Tuning Cobalt–Cobalt Interactions on In2O3-Based Photothermal Catalysts

Rocío Sayago-Carro, Irene Barba-Nieto, Natividad Gómez-Cerezo, José A. Rodriguez, Marcos Fernández-García, Anna Kubacka

ACS Applied Materials & Interfaces· Volume 16· Issue 45

Abstract

The valorization of CO2 is an important challenge within the current panorama, since this molecule is probably the main contributor to climate change. In this study, the synthesis of materials based on a nanostructured batonnet-type indium oxide is carried out. In them, different amounts of Co are introduced, varying between 2 and 8% mol. It is verified that the most active sample in the transformation of carbon dioxide to carbon monoxide contains 6 mol %. of Co. This sample's activity under dual excitation exceeds the thermal counterpart by more than 30%. After carrying out a complete physical and chemical characterization with the help of X-ray absorption spectroscopy and other techniques, it is shown that catalysts with amounts of cobalt equal to or below 4 mol % contain isolated single-atom species, while those with higher amounts of metal display a Co-Co interaction which triggers the evolution of the samples under reaction conditions. The optimum control of this Co-Co interaction and the nature of the final cobalt-containing species determine dual photothermal catalytic properties. This work establishes a structure-activity relationship to interpret the catalytic behavior of highly dispersed subnanometric cobalt species, and thus an avenue to optimize the photothermal valorization of carbon dioxide.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: CO2 Reduction Techniques and Catalysts · Advanced Photocatalysis Techniques · Catalytic Processes in Materials Science

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Instituto de Catálisis y Petroleoquímica, CSIC, C/Marie Curie 2, 28049 Madrid, Spain

Escuela de Doctorado, Universidad Autónoma de Madrid, Ciudad Universitaria de Cantoblanco, C/ Francisco Tomás y Valiente, 1, 28049 Madrid, Spain

Chemistry Division, Brookhaven National Laboratory, Upton, New York 11973, United States

Departamento de Química en Ciencias Farmacéuticas, Facultad de Farmacia, Universidad Complutense de Madrid, Instituto de Investigación Sanitaria Hospital 12 de Octubre, Plaza Ramón y Cajal s/n, 28040Madrid, Spain

Department of Chemistry, Stony Brook University, Stony Brook, New York 11794, United States

Funding

Ministerio de Ciencia, Innovaci?n y Universidades · European Commission · Brookhaven National Laboratory

References (43)

Show source-provided references
1. 10.1038/ncomms424210.1038/ncomms4242 ↗
2. 10.1016/j.checat.2021.01.00310.1016/j.checat.2021.01.003 ↗
3. 10.1016/j.jece.2018.08.06510.1016/j.jece.2018.08.065 ↗
4. 10.1016/j.jechem.2020.01.02310.1016/j.jechem.2020.01.023 ↗
5. 10.1039/D1CS00782C10.1039/D1CS00782C ↗
6. 10.1016/j.joule.2023.12.01310.1016/j.joule.2023.12.013 ↗
7. 10.1002/adfm.20210960010.1002/adfm.202109600 ↗
8. 10.1016/j.cej.2022.13847710.1016/j.cej.2022.138477 ↗
9. 10.1038/s41467-020-16336-z10.1038/s41467-020-16336-z ↗
10. 10.1016/j.apcata.2019.11714410.1016/j.apcata.2019.117144 ↗
11. 10.1016/j.esci.2024.10024610.1016/j.esci.2024.100246 ↗
12. 10.1039/D2YA00190J10.1039/D2YA00190J ↗
13. 10.1016/j.jechem.2020.11.00510.1016/j.jechem.2020.11.005 ↗
14. 10.1016/j.ccr.2022.21479410.1016/j.ccr.2022.214794 ↗
15. 10.1002/cssc.20230140510.1002/cssc.202301405 ↗
16. 10.1002/cssc.20190017510.1002/cssc.201900175 ↗
17. 10.1039/D1CY01067K10.1039/D1CY01067K ↗
18. 10.1021/acs.iecr.3c0329310.1021/acs.iecr.3c03293 ↗
19. 10.1021/acsami.3c1931110.1021/acsami.3c19311 ↗
20. 10.1021/acscatal.9b0496310.1021/acscatal.9b04963 ↗
21. Richards R. · 200610.1201/9781420015751 ↗
22. 10.1016/j.jechem.2023.04.02410.1016/j.jechem.2023.04.024 ↗
23. 10.1021/acsami.4c0572710.1021/acsami.4c05727 ↗
24. Chantler C. T. · 2020
25. 10.1351/PAC-REC-09-09-3610.1351/PAC-REC-09-09-36 ↗
26. 10.1021/acs.nanolett.0c0400810.1021/acs.nanolett.0c04008 ↗
27. 10.1002/aesr.20210016910.1002/aesr.202100169 ↗
28. 10.1016/j.jclepro.2023.13954210.1016/j.jclepro.2023.139542 ↗
29. 10.1016/j.apcatb.2021.12051910.1016/j.apcatb.2021.120519 ↗
30. 10.3938/jkps.64.25410.3938/jkps.64.254 ↗
31. 10.1021/cr030032f10.1021/cr030032f ↗
32. 10.1016/j.gee.2017.02.00110.1016/j.gee.2017.02.001 ↗
33. 10.1002/chem.20110278310.1002/chem.201102783 ↗
34. 10.1021/acscatal.8b0266610.1021/acscatal.8b02666 ↗
35. 10.1021/jp020596810.1021/jp0205968 ↗
36. 10.1103/RevModPhys.53.76910.1103/RevModPhys.53.769 ↗
37. 10.1016/j.physe.2021.11512910.1016/j.physe.2021.115129 ↗
38. 10.1063/1.486510210.1063/1.4865102 ↗
39. 10.1016/j.solmat.2005.11.00710.1016/j.solmat.2005.11.007 ↗
40. 10.1002/cctc.20230112510.1002/cctc.202301125 ↗
41. Moulder, J. F.; Stickle, W. F.; Sobol, P. E. Handbook of X-Ray Photoelectron Spectroscopy: A Reference Book of Standard Data for Use in X-Ray Photoelectron Spectroscopy; Perkin-Elmer, 1993, 83-85.
42. 10.1016/j.fuel.2023.12752810.1016/j.fuel.2023.127528 ↗
43. 10.1016/j.apsusc.2022.15499710.1016/j.apsusc.2022.154997 ↗