TY - JOUR
T1 - Hot-electron transfer in quantum-dot heterojunction films
AU - Grimaldi, Gianluca
AU - Crisp, Ryan W.
AU - Ten Brinck, Stephanie
AU - Zapata, Felipe
AU - Van Ouwendorp, Michiko
AU - Renaud, Nicolas
AU - Kirkwood, Nicholas
AU - Evers, Wiel H.
AU - Kinge, Sachin
AU - Infante, Ivan
AU - Siebbeles, Laurens D.A.
AU - Houtepen, Arjan J.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85048533161&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85048533161&partnerID=8YFLogxK
U2 - 10.1038/s41467-018-04623-9
DO - 10.1038/s41467-018-04623-9
M3 - Article
AN - SCOPUS:85048533161
SN - 2041-1723
VL - 9
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 2310
ER -