Abstract
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.
Original language | English |
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Article number | 2310 |
Journal | Nature Communications |
Volume | 9 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1 Dec 2018 |
Funding
This research is funded by the European Research Council Horizon 2020 ERC Grant Agreement No. 678004 (Doping on Demand), STW (project No. 13903, Stable and NonToxic Nanocrystal Solar Cells) and NWO (Vidi grant, No. 723.013.002). Solrun Gud-jonsdottir is acknowledged for assistance during spectro-electrochemical measurements.
Funders | Funder number |
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European Research Council Horizon 2020 ERC | |
Horizon 2020 Framework Programme | 678004 |
Nederlandse Organisatie voor Wetenschappelijk Onderzoek | 723.013.002 |
Stichting voor de Technische Wetenschappen | 13903 |