Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10773/39455 |
Resumo: | The versatility of several N-doped biochar-supported metal catalysts (M/N-BioC) derived from vineyard pruning waste, to promote circular bioeconomy, was evaluated in catalytic transfer hydrogenation (CTH) of furfural (FF), electrocatalytic oxygen reduction and evolution reactions (ORR and OER). The CTH of FF to prepare high valuable chemicals was performed in the presence of formic acid as hydrogen donor at 160 °C, reaching high conversion (up to 80 %) and selectivities towards furfuryl alcohol (ca. 88 %), establishing a promising catalytic route to valorise a biomass platform molecule using 3d-transition metal-based catalysts in absence of molecular hydrogen. The prepared materials also demonstrated moderate ORR electrocatalytic performance in alkaline medium with diffusion-limiting current densities between -3.48 (Co/N-BioC) and -1.27 mA cm-2 (Cu/N-BioC) and potential onset values of 0.88 ≥ Eonset ≥ 0.66 V vs. RHE. Additionally, the materials tested showed selectivity towards indirect pathway in which O2 is reduced to H2O2 and then further reduced to water with the number of electrons transferred per O2 molecule ranging from 2.1 to 3.6 electrons. The materials also presented moderate OER electrocatalytic performances in alkaline medium, with overpotential values between 0.48 (Co/NBioC) and 0.63 V vs. RHE (Fe/N-BioC) and maximum current densities between 0.28 (BioC) and 42.60 mA cm-2 (Co/N-BioC). This research contributes to the development of a new type of promising (electro)catalyst based on biomass residue for biomass valorisation and energy conversion as a promising contribute to the future of biorefineries implementation. |
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Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactionsBiochar materialsFurfuralCTHElectrocatalytic oxygen reactionsBiorefineryThe versatility of several N-doped biochar-supported metal catalysts (M/N-BioC) derived from vineyard pruning waste, to promote circular bioeconomy, was evaluated in catalytic transfer hydrogenation (CTH) of furfural (FF), electrocatalytic oxygen reduction and evolution reactions (ORR and OER). The CTH of FF to prepare high valuable chemicals was performed in the presence of formic acid as hydrogen donor at 160 °C, reaching high conversion (up to 80 %) and selectivities towards furfuryl alcohol (ca. 88 %), establishing a promising catalytic route to valorise a biomass platform molecule using 3d-transition metal-based catalysts in absence of molecular hydrogen. The prepared materials also demonstrated moderate ORR electrocatalytic performance in alkaline medium with diffusion-limiting current densities between -3.48 (Co/N-BioC) and -1.27 mA cm-2 (Cu/N-BioC) and potential onset values of 0.88 ≥ Eonset ≥ 0.66 V vs. RHE. Additionally, the materials tested showed selectivity towards indirect pathway in which O2 is reduced to H2O2 and then further reduced to water with the number of electrons transferred per O2 molecule ranging from 2.1 to 3.6 electrons. The materials also presented moderate OER electrocatalytic performances in alkaline medium, with overpotential values between 0.48 (Co/NBioC) and 0.63 V vs. RHE (Fe/N-BioC) and maximum current densities between 0.28 (BioC) and 42.60 mA cm-2 (Co/N-BioC). This research contributes to the development of a new type of promising (electro)catalyst based on biomass residue for biomass valorisation and energy conversion as a promising contribute to the future of biorefineries implementation.Elsevier2025-06-01T00:00:00Z2023-06-01T00:00:00Z2023-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/39455eng0920-586110.1016/j.cattod.2023.114080Marques, Inês S.Jarrais, BrunoRamos, RubénAbdelkader-Fernandez, Victor K.Yaremchenko, AlekseyFreire, CristinaFernandes, Diana M.Peixoto, Andreia F.info:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T12:17:09Zoai:ria.ua.pt:10773/39455Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:09:39.966892Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions |
title |
Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions |
spellingShingle |
Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions Marques, Inês S. Biochar materials Furfural CTH Electrocatalytic oxygen reactions Biorefinery |
title_short |
Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions |
title_full |
Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions |
title_fullStr |
Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions |
title_full_unstemmed |
Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions |
title_sort |
Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions |
author |
Marques, Inês S. |
author_facet |
Marques, Inês S. Jarrais, Bruno Ramos, Rubén Abdelkader-Fernandez, Victor K. Yaremchenko, Aleksey Freire, Cristina Fernandes, Diana M. Peixoto, Andreia F. |
author_role |
author |
author2 |
Jarrais, Bruno Ramos, Rubén Abdelkader-Fernandez, Victor K. Yaremchenko, Aleksey Freire, Cristina Fernandes, Diana M. Peixoto, Andreia F. |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Marques, Inês S. Jarrais, Bruno Ramos, Rubén Abdelkader-Fernandez, Victor K. Yaremchenko, Aleksey Freire, Cristina Fernandes, Diana M. Peixoto, Andreia F. |
dc.subject.por.fl_str_mv |
Biochar materials Furfural CTH Electrocatalytic oxygen reactions Biorefinery |
topic |
Biochar materials Furfural CTH Electrocatalytic oxygen reactions Biorefinery |
description |
The versatility of several N-doped biochar-supported metal catalysts (M/N-BioC) derived from vineyard pruning waste, to promote circular bioeconomy, was evaluated in catalytic transfer hydrogenation (CTH) of furfural (FF), electrocatalytic oxygen reduction and evolution reactions (ORR and OER). The CTH of FF to prepare high valuable chemicals was performed in the presence of formic acid as hydrogen donor at 160 °C, reaching high conversion (up to 80 %) and selectivities towards furfuryl alcohol (ca. 88 %), establishing a promising catalytic route to valorise a biomass platform molecule using 3d-transition metal-based catalysts in absence of molecular hydrogen. The prepared materials also demonstrated moderate ORR electrocatalytic performance in alkaline medium with diffusion-limiting current densities between -3.48 (Co/N-BioC) and -1.27 mA cm-2 (Cu/N-BioC) and potential onset values of 0.88 ≥ Eonset ≥ 0.66 V vs. RHE. Additionally, the materials tested showed selectivity towards indirect pathway in which O2 is reduced to H2O2 and then further reduced to water with the number of electrons transferred per O2 molecule ranging from 2.1 to 3.6 electrons. The materials also presented moderate OER electrocatalytic performances in alkaline medium, with overpotential values between 0.48 (Co/NBioC) and 0.63 V vs. RHE (Fe/N-BioC) and maximum current densities between 0.28 (BioC) and 42.60 mA cm-2 (Co/N-BioC). This research contributes to the development of a new type of promising (electro)catalyst based on biomass residue for biomass valorisation and energy conversion as a promising contribute to the future of biorefineries implementation. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-06-01T00:00:00Z 2023-06-01 2025-06-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10773/39455 |
url |
http://hdl.handle.net/10773/39455 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
0920-5861 10.1016/j.cattod.2023.114080 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/embargoedAccess |
eu_rights_str_mv |
embargoedAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799137747193036800 |