Nitrogen-doped biochar-supported metal catalysts: high efficiency in both catalytic transfer hydrogenation of furfural and electrocatalytic oxygen reactions

Detalhes bibliográficos
Autor(a) principal: Marques, Inês S.
Data de Publicação: 2023
Outros Autores: Jarrais, Bruno, Ramos, Rubén, Abdelkader-Fernandez, Victor K., Yaremchenko, Aleksey, Freire, Cristina, Fernandes, Diana M., Peixoto, Andreia F.
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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spelling 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
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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
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
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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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