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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Photocatalytic CO2 reduction over Nb2O5/basic bismuth nitrate nanocomposites

Texto completo
Autor(es):
Oliveira, Jessica A. [1, 2] ; Torres, Juliana A. [1] ; Goncalves, V, Renato ; Ribeiro, Caue [1] ; Nogueira, Francisco G. E. [2] ; Ruotolo, Luis A. M. [2]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Embrapa Instrumentat, Rua 15 Novembro 1452, BR-13560970 Sao Carlos, SP - Brazil
[2] Univ Fed Sao Carlos, Grad Program Chem Engn, Rod Washington Luiz, Km 235, BR-13565905 Sao Carlos, SP - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: Materials Research Bulletin; v. 133, JAN 2021.
Citações Web of Science: 0
Resumo

In this work, CO2 was photocatalytic converted to valuable chemicals using photoactive basic bismuth nitrates (Bi6O(4+x)(OH)((4-x))NO3)((6-x))center dot nH(2)O, x = 0-2, n = 0-3) and niobium pentoxide nanocomposites (BBN/Nb2O5). Milder hydrothermal synthesis (at 120 degrees C) maintained the crystal lattice of the BBN precursor (Bi6O5(-OH)(3)(NO3)(5)center dot 3H(2)O), while the synthesis carried out at 230 degrees C led to lamellar Bi2O2(OH)(NO3). Despite of the sample treated at 230 degrees C did not present the required band edge positions to reduce CO2, all the other materials were active for CO2 photoreduction. CO (similar to 2.8 mu mol g(-1) h(-1)) was identified as the main product, followed by C2H4 (similar to 0.1 mu mol g(-1) h(-1)), with the latter being favored using the nanocomposite produced at 120 degrees C. Scavenger experiments revealed that the photocatalytic mechanism is based on a Z-scheme, where molecules are oxidized in the valence band of Nb2O5 and CO2 is reduced in the conduction band of BBN. (AU)

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