Energy Transfer between Inorganic Perovskite Nanocrystals
Author(s) -
Chris de Weerd,
Leyre Gómez,
Hong Zhang,
Wybren Jan Buma,
Georgian Nedelcu,
Maksym V. Kovalenko,
T. Gregorkiewicz
Publication year - 2016
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/acs.jpcc.6b04768
Subject(s) - nanocrystal , perovskite (structure) , quantum dot , materials science , photovoltaics , band gap , nanotechnology , excited state , energy transfer , energy transformation , halide , optoelectronics , exciton , chemical physics , chemistry , physics , photovoltaic system , atomic physics , inorganic chemistry , condensed matter physics , ecology , biology , crystallography , thermodynamics
Cesium lead halide nanocrystals are a new attractive material for optoelectronic applications since they combine the advantageous properties of perovskites and quantum dots. For future applications in optoelectronics and photovoltaics, an efficient energy and/or carrier exchange is a necessary condition. Here, we explicitly demonstrate nonradiative energy transfer for colloidal CsPbBr3 nanocrystals. Using time-resolved optical characterization of purposefully prepared batches of nanocrystals with different sizes, we identify the energy transfer which can be driven by the concentration gradient of excited nanocrystals as well as by the bandgap energy difference. The latter process moves the energy from smaller to larger nanocrystals and opens a possibility of directional streaming of the excitation energy in these materials. The observed energy transfer is enabled in the colloids by proximity of individual nanocrystals due to clustering.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom