CO₂ Photoreduction Product Selectivity with TiO₂-Cu Nanocatalysts under Different Reaction Media

Autor(es)

Nascimento, Victor R. S. ; Torres, Juliana A. ; Iga, Gustavo D. ; dos Santos, Allef Leite ; Egues, Silvia M. ; Filho, Jose B. G. ; Ferreira, Luiz F. R. ; Ribeiro, Caue

• Tipo de documento: Artigo Científico
• Fonte: CHEMCATCHEM; v. 16, n. 11, p. 12-pg., 2024-03-04.

Resumo

This study explores photocatalytic conversion of CO2 using TiO2-Cu heterojunctions with different Cu contents and investigates influence of different reaction media on the process efficiency. The use of KOH favored liquid products, especially ethanol. An analysis of H-2 production as the main competitive reaction was done. Sodium oxalate led to an increase in H-2 evolution by approximately 600 mu mol g-(1) compared to pure water, in the presence of CO2 in the reaction medium, but the blank test (without CO2) indicates a lower H-2 yield (similar to 136 mu mol g(-1)), which suggests that the competitive reaction with CO2 also plays a role in H-2 production. This role was related to the decrease of the initial pH from approximately 8.5 to 5.2, stabilizing at 5.5 at the end of the 6 h reaction. In an environment saturated with N-2, the pH increases to 9 and stabilizes at 7.8 at the end of the process. In the presence of acetic acid, both CO and H-2 production were suppressed, with a significant increase in the selectivity for methane via cleavage of the acid's carbon bond. The findings underscore the importance of optimizing reaction conditions to achieve higher yields of desired products in the photocatalytic conversion of CO2. (AU)

• Processo FAPESP: 22/07347-5 - Estudo da reversibilidade redox de catalisadores à base de cobre para aplicação em um sistema foto-termocatalítico para hidrogenação de co2 day-and-night.
• Beneficiário: Gustavo Duran Iga
• Modalidade de apoio: Bolsas no Brasil - Doutorado
• Processo FAPESP: 18/01258-5 - Novos processos catalíticos e fotocatalíticos para a conversão direta de metano e CO2 em produtos
• Beneficiário: José Maria Correa Bueno
• Modalidade de apoio: Auxílio à Pesquisa - Temático