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| Registros recuperados : 46 | |
| 3. |  | SILVA, G. T. S. T. da; CARVALHO, K. T.; LOPES, O. F.; OLIVEIRA, C. R. de. Photocatalytic degradation of organic compounds over g-C3N4/Nb2O5 heterostructures. In: INTERNATIONAL CONGRESS ON CERAMICS, 7., CONGRESSO BRASILEIRO DE CERÂMICA, 62., 2018, Foz do Iguaçu. Resumos... Foz do Iguaçu: Metallum, 2018. p. 379.| Biblioteca(s): Embrapa Instrumentação. |
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| 5. | | TORRES, J. A.; NOGUEIRA, A. E.; SILVA, G. T. S. T.; OLIVEIRA, C. R. de. Redução fotocatalítica de CO2: influência do caráter básico do MgO. In: WORKSHOP DA REDE DE NANOTECNOLOGIA APLICADA AO AGRONEGÓCIO, 9., 2017, São Carlos. Anais ... São Carlos: Embrapa Instrumentação, 2017. p.414-417. Editores: Caue Ribeiro de Oliveira, Elaine Cristina Paris, Luiz Henrique Capparelli Mattoso, Marcelo Porto Bemquerer, Maria Alice Martins, Odílio Benedito Garrido de Assis.| Biblioteca(s): Embrapa Instrumentação. |
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| 8. | | MENDONÇA, V. R.; LOPES, O. F.; NOGUEIRA, A. E.; SILVA, G. T. S. T.; RIBEIRO, C. Challenges of synthesis and environmental applications of metal-free nano-heterojunctions. In: INAMUDDIN, G. S.; KUMAR, A.; LICHITFOUSE, E.; ASIRI, A. M. (Eds.). Nanophotocatalysis and Environmental Applications: Spinger, Cham, 2019. 108-130 Chapter 4| Biblioteca(s): Embrapa Instrumentação. |
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| 12. | | SILVA, G. T. S. T.; CARVALHO, K. T. G.; LOPES, O. F.; OLIVEIRA, C. R. de. Síntese sonoquímica de heteroestruturas g-C3N4/Nb2O5: avaliação da perfomance fotocatalítica para degradação de poluentes orgânicos. In: WORKSHOP DA REDE DE NANOTECNOLOGIA APLICADA AO AGRONEGÓCIO, 9., 2017, São Carlos. Anais ... São Carlos: Embrapa Instrumentação, 2017. p.487-490. Editores: Caue Ribeiro de Oliveira, Elaine Cristina Paris, Luiz Henrique Capparelli Mattoso, Marcelo Porto Bemquerer, Maria Alice Martins, Odílio Benedito Garrido de Assis.| Biblioteca(s): Embrapa Instrumentação. |
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| 13. | | BOLFE, E. L.; PENA JUNIOR, M. A. G.; CONTINI, E.; D'OLIVEIRA, F. M.; SILVA, G. T. S. da. Base de dados da agropecuária brasileira: planejamento estratégico e desenvolvimento. Brazilian Journal of Development, Curitiba, v. 5, n. 1, p. 201-214, jan. 2019.| Biblioteca(s): Embrapa Unidades Centrais. |
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| 15. | | MENDES, J. O. S.; CARVALHO, K. T. G.; SILVA, G. T. S. T. da; OLIVEIRA, C. R. de. Studies of photocatalytic reduction of carbon dioxide for renewable fuel production using niobium oxide. In: INTERNATIONAL CONGRESS ON CERAMICS, 7., CONGRESSO BRASILEIRO DE CERÂMICA, 62., 2018, Foz do Iguaçu. Resumos... Foz do Iguaçu: Metallum, 2018. p. 381.| Biblioteca(s): Embrapa Instrumentação. |
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| 16. | | NOGUEIRA, A. E.; SILVA, G. T. S. T.; OLIVEIRA, J. A.; TORRES, J. A.; SILVA, M.; CARMO, M.; RIBEIRO, C. Unveiling copper oxide role in CO2 photoreduction process - catalyst or reactant? In: SPRING MEETING OF THE EUROPEAN MATERIALS RESEARCH SOCIETY, 37. 2019, Nice, França, 2019.| Biblioteca(s): Embrapa Instrumentação. |
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| 18. | | SILVA, G. T. S. T.; NOGUEIRA, A. E.; OLIVEIRA, J. A.; JODAR, L. V.; TORRES, J. A.; OLIVEIRA, C. R. de. Influência da acidez superficial da niobia para o processo de fotorredução de CO2. In: WORKSHOP DA REDE DE NANOTECNOLOGIA APLICADA AO AGRONEGÓCIO, 9., 2017, São Carlos. Anais ... São Carlos: Embrapa Instrumentação, 2017. p.495-498. Editores: Caue Ribeiro de Oliveira, Elaine Cristina Paris, Luiz Henrique Capparelli Mattoso, Marcelo Porto Bemquerer, Maria Alice Martins, Odílio Benedito Garrido de Assis.| Biblioteca(s): Embrapa Instrumentação. |
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| 19. | | CARVALHO JUNIOR, P. S.; DINIZ, L. F.; SILVA, G. T. S. T. da; COUTINHO, N. D.; SANTOS, P. G. dos; CARVALHO-SILVA, V. H.; RIBEIRO, C.; ELLENA, J. Amino - imino tautomerism in the salt formation of Albendazole: Hydrobromide and nitrate salts. Crystal Growth & Design, v. 21, 2021. 1122?1135| Biblioteca(s): Embrapa Instrumentação. |
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| 20. | | NOGUEIRA, A. E.; RIBEIRO, L. S.; GORUP, L. F.; SILVA, G. T. S. T.; SILVA, F. F. B.; OLIVEIRA, C. R. de; CAMARGO, E. R. New approach of the oxidant peroxo method (OPM) route to obtain Ti(OH)4 nanoparticles with high photocatalytic activity under visible radiation. International Journal of Photoenergy, v. 2018, ID 6098302, 10 p., 2018.| Biblioteca(s): Embrapa Instrumentação. |
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| Registros recuperados : 46 | |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Instrumentação. Para informações adicionais entre em contato com cnpdia.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Instrumentação. |
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Data corrente: |
02/10/2023 |
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Data da última atualização: |
02/10/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 1 |
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Autoria: |
SILVA, R. M. e; SOUZA, F. L.; DIAS, E.; SILVA, G. T. S. T. da; DÚRAN, F. E.; REGO, A.; HIGGINS, D.; RIBEIRO, C. |
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Afiliação: |
Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada; Department of Chemistry and Molecular Physics, Institute of Chemistry of Sao Carlos, University of Sao Paulo, Brazil; Department of Chemistry and Molecular Physics, Institute of Chemistry of Sao Carlos, University of Sao Paulo, Brazil; Interdisciplinary Laboratory of Electrochemistry and Ceramics, Department of Chemistry, Federal University of Sao Carlos; Department of Fuel and Hydrogen Cells, Nuclear and Energy Research Institute; Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada; Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada; CAUE RIBEIRO DE OLIVEIRA, CNPDIA. |
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Título: |
The role of TiO2:SnO2 heterojunction for partial oxidation of methane by photoelectrocatalytic process at room temperature. |
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Ano de publicação: |
2023 |
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Fonte/Imprenta: |
Journal of Alloys and Compounds, v. 968, 172090, 2023. |
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Páginas: |
7 p. |
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ISSN: |
0925-8388 |
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DOI: |
https://doi.org/10.1016/j.jallcom.2023.172090 |
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Idioma: |
Inglês |
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Conteúdo: |
hane into hydrocarbons using photoelectrochemical routes is attractive from a sustainability point of view owing to the possibility of using renewable energy (i.e., solar illumination) to activate this stable molecule. However, the process demands the development of novel catalysts that can promote methane activation and oxidation in a controlled manner to increase energy conversion efficiency. Herein, we demonstrated that semiconductor heterostructures improved charge separation compared to the individual materials alone. A more effortless transfer between bands favors the separation of the electron-hole (e− /h+) pairs generated by the photoelectrocatalytic system and prevents them from recombining. This process produces reactive oxygens, essential to driving methane oxidation conversion of the C?H bond cleavage. TiO2:SnO2 semiconductor heterojunction catalysts in film shape were investigated for methane oxidation via a photoelectrocatalytic process. The methane oxidation reactions were carried out in an inflow and sealed electrochemical system for 1 h. Liquid-state nuclear magnetic resonance revealed methanol and acetic acid as the main liquid products, where the TiO2:SnO2 heterojunction exhibited better performance with values of 30 and 8 µmol. cm− 2 .h− 1 , respectively. Compared to their materials alone, the superior performance of the TiO2:SnO2 heterojunction is attributed to the formation of heterostructure type II that enables a more effortless transfer between bands, facilitating the separation of the generated e− /h+ pairs under UV-Vis irradiation. The outcomes achieved here will motivate further studies for developing semiconductor heterojunction structure catalysts in photoelectrocatalysis to partially oxidize methane into valuable chemicals. Menoshane into hydrocarbons using photoelectrochemical routes is attractive from a sustainability point of view owing to the possibility of using renewable energy (i.e., solar illumination) to activate this stable molecule. However, the process demands the development of novel catalysts that can promote methane activation and oxidation in a controlled manner to increase energy conversion efficiency. Herein, we demonstrated that semiconductor heterostructures improved charge separation compared to the individual materials alone. A more effortless transfer between bands favors the separation of the electron-hole (e− /h+) pairs generated by the photoelectrocatalytic system and prevents them from recombining. This process produces reactive oxygens, essential to driving methane oxidation conversion of the C?H bond cleavage. TiO2:SnO2 semiconductor heterojunction catalysts in film shape were investigated for methane oxidation via a photoelectrocatalytic process. The methane oxidation reactions were carried out in an inflow and sealed electrochemical system for 1 h. Liquid-state nuclear magnetic resonance revealed methanol and acetic acid as the main liquid products, where the TiO2:SnO2 heterojunction exhibited better performance with values of 30 and 8 µmol. cm− 2 .h− 1 , respectively. Compared to their materials alone, the superior performance of the TiO2:SnO2 heterojunction is attributed to the formation of heterostructure type II that enables a more effortless tran... Mostrar Tudo |
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Palavras-Chave: |
CH4 oxidation; Methane oxidation; Photoelectrocatalysis; TiO2 SnO2 heterojunction. |
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Categoria do assunto: |
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Marc: |
LEADER 02695naa a2200289 a 4500
001 2157017
005 2023-10-02
008 2023 bl uuuu u00u1 u #d
022 $a0925-8388
024 7 $ahttps://doi.org/10.1016/j.jallcom.2023.172090$2DOI
100 1 $aSILVA, R. M. e
245 $aThe role of TiO2$bSnO2 heterojunction for partial oxidation of methane by photoelectrocatalytic process at room temperature.$h[electronic resource]
260 $c2023
300 $a7 p.
520 $ahane into hydrocarbons using photoelectrochemical routes is attractive from a sustainability point of view owing to the possibility of using renewable energy (i.e., solar illumination) to activate this stable molecule. However, the process demands the development of novel catalysts that can promote methane activation and oxidation in a controlled manner to increase energy conversion efficiency. Herein, we demonstrated that semiconductor heterostructures improved charge separation compared to the individual materials alone. A more effortless transfer between bands favors the separation of the electron-hole (e− /h+) pairs generated by the photoelectrocatalytic system and prevents them from recombining. This process produces reactive oxygens, essential to driving methane oxidation conversion of the C?H bond cleavage. TiO2:SnO2 semiconductor heterojunction catalysts in film shape were investigated for methane oxidation via a photoelectrocatalytic process. The methane oxidation reactions were carried out in an inflow and sealed electrochemical system for 1 h. Liquid-state nuclear magnetic resonance revealed methanol and acetic acid as the main liquid products, where the TiO2:SnO2 heterojunction exhibited better performance with values of 30 and 8 µmol. cm− 2 .h− 1 , respectively. Compared to their materials alone, the superior performance of the TiO2:SnO2 heterojunction is attributed to the formation of heterostructure type II that enables a more effortless transfer between bands, facilitating the separation of the generated e− /h+ pairs under UV-Vis irradiation. The outcomes achieved here will motivate further studies for developing semiconductor heterojunction structure catalysts in photoelectrocatalysis to partially oxidize methane into valuable chemicals.
653 $aCH4 oxidation
653 $aMethane oxidation
653 $aPhotoelectrocatalysis
653 $aTiO2 SnO2 heterojunction
700 1 $aSOUZA, F. L.
700 1 $aDIAS, E.
700 1 $aSILVA, G. T. S. T. da
700 1 $aDÚRAN, F. E.
700 1 $aREGO, A.
700 1 $aHIGGINS, D.
700 1 $aRIBEIRO, C.
773 $tJournal of Alloys and Compounds$gv. 968, 172090, 2023.
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