The Facile Microwave-Assisted Coprecipitation Route to Obtain Polyoxoniobate (Na7(H3O)Nb6O19·14H2O) Nanorods Modified with Copper for CO2 Photoreduction

Author:

Souza Joelma R. C.1,Torres Juliana A.2,Ribeiro Lucas S.3ORCID,Filho Jose B. G.1,Santos Fabiana L.1,Malgioglio Nicholas4,Gorup Luiz Fernando356ORCID,Pinto Alexandre H.4ORCID,Nogueira André E.1ORCID

Affiliation:

1. Department of Chemistry, Institute of Exact and Biological Sciences (ICEB), Federal University of Ouro Preto—UFOP, Ouro Preto 35400-000, Brazil

2. Embrapa Instrumentation, São Carlos 13560-970, Brazil

3. Interdisciplinary Laboratory of Electrochemistry and Ceramics (LIEC), Department of Chemistry, UFSCar—Federal University of São Carlos, São Carlos 13565-905, Brazil

4. Department of Chemistry & Biochemistry, Manhattan College, 4513 Manhattan College Parkway, Riverdale, NY 10471, USA

5. Institute of Chemistry, Federal University of Alfenas, Alfenas 37130-001, Brazil

6. School of Chemistry and Food Science, Federal University of Rio Grande, Rio Grande 96203-900, Brazil

Abstract

The CO2 reduction by solar means has been discussed as an alternative to emission abatement, a fundamental topic for sustainable, carbon-free production in the future. However, the choice of efficient systems, starting with the catalysts, is still a critical issue, especially due to the poor activity of available options. Polyoxometalates have been extensively studied as promising photocatalysts due to their semiconducting properties. Nevertheless, the synthetic conditions of polyoxoniobate are stringent due to the low reaction activity of Nb species, the lack of soluble precursors, and the narrow pH range. Unlike the literature, in the present study, we report a simple polyoxoniobate synthesis method. This synthesis method has some remarkable features, such as low processing time and temperature and good activity and selectivity in the CO2 photoreduction process. The results revealed an outstanding efficiency for the CO2 reduction reaction with a high selectivity of CO2 to CO conversion (92.5%). Furthermore, C2 compounds (e.g., acetate) were produced in the liquid phase of the reaction system. Our findings are significant for indicating the potential of polyoxoniobate for CO2 photoreduction, which opens a way to control competitive reactions with synthesis, leading to higher selectivity.

Funder

FAPEMIG

National Council for Scientific and Technological Development-CNPq, Ministry of Science, Technology and Innovation-MCTI

FAPESP

CAPES

Publisher

MDPI AG

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