TY - JOUR
T1 - Luminescence upconversion in colloidal double quantum dots
AU - Deutsch, Zvicka
AU - Neeman, Lior
AU - Oron, Dan
N1 - Minerva Foundation; Leona M. and Harry B. Helmsley charitable trust; European Research Council [SINSLIM 258221]The authors acknowledge financial support from the Minerva Foundation, the Leona M. and Harry B. Helmsley charitable trust, and the European Research Council (starting investigator grant SINSLIM 258221). D.O. is the incumbent of the Recanati Career Development Chair in Energy Research.
PY - 2013/9
Y1 - 2013/9
N2 - Luminescence upconversion nanocrystals capable of converting two low-energy photons into a single photon at a higher energy are sought-after for a variety of applications, including bioimaging and photovoltaic light harvesting. Currently available systems, based on rare-earth-doped dielectrics, are limited in both tunability and absorption cross-section. Here we present colloidal double quantum dots as an alternative nanocrystalline upconversion system, combining the stability of an inorganic crystalline structure with the spectral tunability afforded by quantum confinement. By tailoring its composition and morphology, we form a semiconducting nanostructure in which excited electrons are delocalized over the entire structure, but a double potential well is formed for holes. Upconversion occurs by excitation of an electron in the lower energy transition, followed by intraband absorption of the hole, allowing it to cross the barrier to a higher energy state. An overall conversion efficiency of 0.1% per double excitation event is achieved.
AB - Luminescence upconversion nanocrystals capable of converting two low-energy photons into a single photon at a higher energy are sought-after for a variety of applications, including bioimaging and photovoltaic light harvesting. Currently available systems, based on rare-earth-doped dielectrics, are limited in both tunability and absorption cross-section. Here we present colloidal double quantum dots as an alternative nanocrystalline upconversion system, combining the stability of an inorganic crystalline structure with the spectral tunability afforded by quantum confinement. By tailoring its composition and morphology, we form a semiconducting nanostructure in which excited electrons are delocalized over the entire structure, but a double potential well is formed for holes. Upconversion occurs by excitation of an electron in the lower energy transition, followed by intraband absorption of the hole, allowing it to cross the barrier to a higher energy state. An overall conversion efficiency of 0.1% per double excitation event is achieved.
UR - http://www.scopus.com/inward/record.url?scp=84883744133&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/nnano.2013.146
DO - https://doi.org/10.1038/nnano.2013.146
M3 - مقالة
SN - 1748-3387
VL - 8
SP - 649
EP - 653
JO - Nature Nanotechnology
JF - Nature Nanotechnology
IS - 9
ER -