Hybrid biological/inorganic photocathode for H2 production based on a NiFeSe hydrogenase immobilized on electrodeposited CuGaS2

In order to mitigate global warming and pollution problems, new energy vectors need to be developed towards a fossil fuel-free society. Hydrogen is a great candidate for the role, since it can be cleanly obtained from water splitting. However, finding an efficient method that allows diminishing the...

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Detalles Bibliográficos
Autores: Luna-López, Gabriel, Sainz, Raquel, Coito, A.M., Pichon, C., Iglesias Juez, Ana, Pereira, I.A.C., López de Lacey, Antonio, Pita, Marcos
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2023
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/358731
Acceso en línea:http://hdl.handle.net/10261/358731
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85166670268&doi=10.1016%2fj.cattod.2023.114281&partnerID=40&md5=ff1568ca7d7f5fb476b1fd97277118d0
Access Level:acceso abierto
Palabra clave:Photocatalysis
Biocatalysis
Copper gallium sulfide
Hydrogen
Hydrogenase
Descripción
Sumario:In order to mitigate global warming and pollution problems, new energy vectors need to be developed towards a fossil fuel-free society. Hydrogen is a great candidate for the role, since it can be cleanly obtained from water splitting. However, finding an efficient method that allows diminishing the high potentials required for the reaction is still a challenge to overcome. In order to tackle this task, a combination of a redox biocatalyst and an inorganic semiconductor that harnesses sunlight to enhance the H2 photoelectrochemical production has been studied. For this endeavor, we have developed a photocathode based on the p-type semiconductor copper gallium sulfide and the Desulfovibrio vulgaris Hildenborough NiFeSe-hydrogenase where the photoexcited semiconductor transfers excited electrons to the enzyme upon visible irradiation. The system is capable of producing photoelectrochemical biocatalytic proton reduction to H2 without any sacrificial agent while providing an approximately 400 mV decrease of the applied potential. © 2023 The Authors