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A robust ALD-protected silicon-based hybrid photoelectrode for hydrogen evolution under aqueous conditions

Hydrogen production through direct sunlight-driven water splitting in photo-electrochemical cells (PECs) is a promising solution for energy sourcing. PECs need to fulfill three criteria: sustainability, cost-effectiveness and stability. Here we report an efficient and stable photocathode platform fo...

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Detalles Bibliográficos
Autores principales: Chandrasekaran, Soundarrajan, Kaeffer, Nicolas, Cagnon, Laurent, Aldakov, Dmitry, Fize, Jennifer, Nonglaton, Guillaume, Baleras, François, Mailley, Pascal, Artero, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482884/
https://www.ncbi.nlm.nih.gov/pubmed/31057774
http://dx.doi.org/10.1039/c8sc05006f
Descripción
Sumario:Hydrogen production through direct sunlight-driven water splitting in photo-electrochemical cells (PECs) is a promising solution for energy sourcing. PECs need to fulfill three criteria: sustainability, cost-effectiveness and stability. Here we report an efficient and stable photocathode platform for H(2) evolution based on Earth-abundant elements. A p-type silicon surface was protected by atomic layer deposition (ALD) with a 15 nm TiO(2) layer, on top of which a 300 nm mesoporous TiO(2) layer was spin-coated. The cobalt diimine–dioxime molecular catalyst was covalently grafted onto TiO(2) through phosphonate anchors and an additional 0.2 nm ALD-TiO(2) layer was applied for stabilization. This assembly catalyzes water reduction into H(2) in phosphate buffer (pH 7) with an onset potential of +0.47 V vs. RHE. The resulting current density is –1.3 ± 0.1 mA cm(–2) at 0 V vs. RHE under AM 1.5 solar irradiation, corresponding to a turnover number of 260 per hour of operation and a turnover frequency of 0.071 s(–1).