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Hot-electron transfer in quantum-dot heterojunction films

Thermalization losses limit the photon-to-power conversion of solar cells at the high-energy side of the solar spectrum, as electrons quickly lose their energy relaxing to the band edge. Hot-electron transfer could reduce these losses. Here, we demonstrate fast and efficient hot-electron transfer be...

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Detalles Bibliográficos
Autores principales: Grimaldi, Gianluca, Crisp, Ryan W., ten Brinck, Stephanie, Zapata, Felipe, van Ouwendorp, Michiko, Renaud, Nicolas, Kirkwood, Nicholas, Evers, Wiel H., Kinge, Sachin, Infante, Ivan, Siebbeles, Laurens D. A., Houtepen, Arjan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998019/
https://www.ncbi.nlm.nih.gov/pubmed/29899361
http://dx.doi.org/10.1038/s41467-018-04623-9
Descripción
Sumario:Thermalization losses limit the photon-to-power conversion of solar cells at the high-energy side of the solar spectrum, as electrons quickly lose their energy relaxing to the band edge. Hot-electron transfer could reduce these losses. Here, we demonstrate fast and efficient hot-electron transfer between lead selenide and cadmium selenide quantum dots assembled in a quantum-dot heterojunction solid. In this system, the energy structure of the absorber material and of the electron extracting material can be easily tuned via a variation of quantum-dot size, allowing us to tailor the energetics of the transfer process for device applications. The efficiency of the transfer process increases with excitation energy as a result of the more favorable competition between hot-electron transfer and electron cooling. The experimental picture is supported by time-domain density functional theory calculations, showing that electron density is transferred from lead selenide to cadmium selenide quantum dots on the sub-picosecond timescale.