Electrocatalysis of Formate Dehydrogenase Towards CO2 Reduction

Bibliographic Details
Main Author: Baptista, Rita Helena Duarte
Publication Date: 2021
Format: Master thesis
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10362/110680
Summary: The continuous strong growth of CO2 emissions and the intensification of environmental impacts caused by this gas have aroused an increasing interest in the development of strategies to transform CO2. Formate dehydrogenases (FDH) are enzymes that perform the reversible interconversion of formate to CO2, hence these biocatalysts can transform CO2 into a compound that can be used either as a biofuel or as chemical precursor for sustainable chemical synthesis. Reports on direct electrochemical approaches, avoiding kinetic limitations of the mediating molecules and additional steps of cofactors regeneration, have been scarce until recently. In this Thesis, the electrochemical characterisation of the molybdenum-containing FDH from Desulfovibrio desulfuricans (DdFDH) was accomplished through non-mediated methods, in the absence of added substrates (non-turnover conditions), for the enzyme physically adsorbed onto a pyrolytic graphite electrode, at pH 6.5. A redox process with formal potential of -124 ± 11 mV vs NHE was assigned to the redox pair Mo (VI/IV) of the active centre. The heterogeneous electron transfer rate constant increased with the scan rate, which is indicative of a good communication between the enzyme and the electrode. The DdFDH catalytic response towards CO2 reduction was attained without mediators as well, upon the addition of saturated CO2 solution and sodium carbonate solution for the DdFDH adsorbed onto a stationary pyrolytic graphite electrode. The electrocatalysis towards CO2 reduction was also attained for DdFDH physically adsorbed on glassy carbon and graphite, under the hydrodynamic regime, and for the DdFDH encapsulated on felt carbon, a gas diffusion electrode.
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spelling Electrocatalysis of Formate Dehydrogenase Towards CO2 ReductionCO2 valorisationElectrocatalysisFormate dehydrogenaseProtein electrochemistryDomínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e TecnologiasThe continuous strong growth of CO2 emissions and the intensification of environmental impacts caused by this gas have aroused an increasing interest in the development of strategies to transform CO2. Formate dehydrogenases (FDH) are enzymes that perform the reversible interconversion of formate to CO2, hence these biocatalysts can transform CO2 into a compound that can be used either as a biofuel or as chemical precursor for sustainable chemical synthesis. Reports on direct electrochemical approaches, avoiding kinetic limitations of the mediating molecules and additional steps of cofactors regeneration, have been scarce until recently. In this Thesis, the electrochemical characterisation of the molybdenum-containing FDH from Desulfovibrio desulfuricans (DdFDH) was accomplished through non-mediated methods, in the absence of added substrates (non-turnover conditions), for the enzyme physically adsorbed onto a pyrolytic graphite electrode, at pH 6.5. A redox process with formal potential of -124 ± 11 mV vs NHE was assigned to the redox pair Mo (VI/IV) of the active centre. The heterogeneous electron transfer rate constant increased with the scan rate, which is indicative of a good communication between the enzyme and the electrode. The DdFDH catalytic response towards CO2 reduction was attained without mediators as well, upon the addition of saturated CO2 solution and sodium carbonate solution for the DdFDH adsorbed onto a stationary pyrolytic graphite electrode. The electrocatalysis towards CO2 reduction was also attained for DdFDH physically adsorbed on glassy carbon and graphite, under the hydrodynamic regime, and for the DdFDH encapsulated on felt carbon, a gas diffusion electrode.Cordas, CristinaMaia, LuísaRUNBaptista, Rita Helena Duarte2022-10-01T00:31:12Z2021-01-1420212021-01-14T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10362/110680enginfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-22T17:49:59Zoai:run.unl.pt:10362/110680Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:21:14.340303Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Electrocatalysis of Formate Dehydrogenase Towards CO2 Reduction
title Electrocatalysis of Formate Dehydrogenase Towards CO2 Reduction
spellingShingle Electrocatalysis of Formate Dehydrogenase Towards CO2 Reduction
Baptista, Rita Helena Duarte
CO2 valorisation
Electrocatalysis
Formate dehydrogenase
Protein electrochemistry
Domínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e Tecnologias
title_short Electrocatalysis of Formate Dehydrogenase Towards CO2 Reduction
title_full Electrocatalysis of Formate Dehydrogenase Towards CO2 Reduction
title_fullStr Electrocatalysis of Formate Dehydrogenase Towards CO2 Reduction
title_full_unstemmed Electrocatalysis of Formate Dehydrogenase Towards CO2 Reduction
title_sort Electrocatalysis of Formate Dehydrogenase Towards CO2 Reduction
author Baptista, Rita Helena Duarte
author_facet Baptista, Rita Helena Duarte
author_role author
dc.contributor.none.fl_str_mv Cordas, Cristina
Maia, Luísa
RUN
dc.contributor.author.fl_str_mv Baptista, Rita Helena Duarte
dc.subject.por.fl_str_mv CO2 valorisation
Electrocatalysis
Formate dehydrogenase
Protein electrochemistry
Domínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e Tecnologias
topic CO2 valorisation
Electrocatalysis
Formate dehydrogenase
Protein electrochemistry
Domínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e Tecnologias
description The continuous strong growth of CO2 emissions and the intensification of environmental impacts caused by this gas have aroused an increasing interest in the development of strategies to transform CO2. Formate dehydrogenases (FDH) are enzymes that perform the reversible interconversion of formate to CO2, hence these biocatalysts can transform CO2 into a compound that can be used either as a biofuel or as chemical precursor for sustainable chemical synthesis. Reports on direct electrochemical approaches, avoiding kinetic limitations of the mediating molecules and additional steps of cofactors regeneration, have been scarce until recently. In this Thesis, the electrochemical characterisation of the molybdenum-containing FDH from Desulfovibrio desulfuricans (DdFDH) was accomplished through non-mediated methods, in the absence of added substrates (non-turnover conditions), for the enzyme physically adsorbed onto a pyrolytic graphite electrode, at pH 6.5. A redox process with formal potential of -124 ± 11 mV vs NHE was assigned to the redox pair Mo (VI/IV) of the active centre. The heterogeneous electron transfer rate constant increased with the scan rate, which is indicative of a good communication between the enzyme and the electrode. The DdFDH catalytic response towards CO2 reduction was attained without mediators as well, upon the addition of saturated CO2 solution and sodium carbonate solution for the DdFDH adsorbed onto a stationary pyrolytic graphite electrode. The electrocatalysis towards CO2 reduction was also attained for DdFDH physically adsorbed on glassy carbon and graphite, under the hydrodynamic regime, and for the DdFDH encapsulated on felt carbon, a gas diffusion electrode.
publishDate 2021
dc.date.none.fl_str_mv 2021-01-14
2021
2021-01-14T00:00:00Z
2022-10-01T00:31:12Z
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