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Multilayered Plasmonic Heterostructure of Gold and Titania Nanoparticles for Solar Fuel Production

Solar fuel production via photoelectrochemical (PEC) water splitting has attracted great attention as an approach to storing solar energy. However, a wide range of light-harvesting materials is unstable when exposed to light and oxidative conditions. Here we report a robust, multilayered plasmonic h...

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Detalles Bibliográficos
Autores principales: Kim, Jeonga, Son, Ho Yeon, Nam, Yoon Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041279/
https://www.ncbi.nlm.nih.gov/pubmed/29993015
http://dx.doi.org/10.1038/s41598-018-28789-w
Descripción
Sumario:Solar fuel production via photoelectrochemical (PEC) water splitting has attracted great attention as an approach to storing solar energy. However, a wide range of light-harvesting materials is unstable when exposed to light and oxidative conditions. Here we report a robust, multilayered plasmonic heterostructure for water oxidation using gold nanoparticles (AuNPs) as light-harvesting materials via localized surface plasmon resonance (LSPR). The multilayered heterostructure is fabricated using layer-by-layer self-assembly of AuNPs and TiO(2) nanoparticles (TNPs). Plasmon-induced hot electrons are transferred from AuNPs to TNPs over the Au/TiO(2) Schottky barrier, resulting in charge separation of hot carriers. Plasmonic photoanodes for water oxidation are completed by incorporating a Co-based oxygen-evolving catalyst on the multilayered heterostructure to scavenge hot holes. Light absorption capability and PEC properties of the photoanodes are investigated as a function of the number of AuNP/TNP bilayers. The PEC properties exhibits dependence on the number of the bilayers, which is affected by charge transport within the multilayered heterostructures. Photocurrent density and decrease in impedance by irradiation indicates significant photoactivity by LSPR excitation.