The optical properties of PbSe/CdSe core/shell quantum dots with core sizes smaller than 4 nm in the 5-300 K range are reported. The photoluminescence spectra show two peaks, which become increasingly separated in energy as the core diameter is reduced below 4 nm. It is shown that these peaks are due to intrinsic exciton transitions in each quantum dot, rather than emission from different quantum dot sub-ensembles. Most likely, the energy separation between the peaks is due to inter-valley coupling between the L-points of PbSe. The temperature dependence of the relative intensities of the peaks implies that the two emitting states are not in thermal equilibrium and that dark exciton states must play an important role.
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http://dx.doi.org/10.1002/smll.201101819 | DOI Listing |
Nat Mater
August 2023
Nanotechnology and Advanced Spectroscopy Team, C-PCS, Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM, USA.
Carrier multiplication is a process whereby a kinetic energy of a carrier relaxes via generation of additional electron-hole pairs (excitons). This effect has been extensively studied in the context of advanced photoconversion as it could boost the yield of generated excitons. Carrier multiplication is driven by carrier-carrier interactions that lead to excitation of a valence-band electron to the conduction band.
View Article and Find Full Text PDFJ Phys Chem Lett
April 2021
Department of Mechanical Engineering, Toyama National College of Technology, 13 Hongo-machi, Toyama 939-8630, Japan.
Photoluminescence (PL) emission of colloidal PbSe/CdSe core/shell quantum dots (QDs, CdSe shell thickness: 0.2 nm) at the lowest exciton state was investigated at room temperature and varying inter-QD distance ( = 7-240 nm) by changing the QD concentration. A distinct enhancement of the valley splitting of PbSe QDs was observed upon reducing .
View Article and Find Full Text PDFJ Phys Chem Lett
June 2020
Chemistry & Biochemistry Department, North Dakota State University, Fargo, North Dakota 58108, United States.
We study the impact of the chemical composition on phonon-mediated exciton relaxation in the core/shell quantum dots (QDs), with 1 nm core made of PbX and the monolayer shell made of CdX, where X = S and Se. For this, time-domain nonadiabatic molecular dynamics (NAMD) based on density functional theory (DFT) and surface hopping techniques are applied. Simulations reveal twice faster energy relaxation in PbS/CdS than PbSe/CdSe because of dominant couplings to higher-energy optical phonons in structures with sulfur anions.
View Article and Find Full Text PDFACS Nano
December 2016
Center for Advanced Solar Photophysics, Chemistry Division, Los Alamos National Laboratory , Los Alamos, New Mexico 87545, United States.
One source of efficiency losses in photovoltaic cells is their transparency toward solar photons with energies below the band gap of the absorbing layer. This loss can be reduced using a process of up-conversion whereby two or more sub-band-gap photons generate a single above-gap exciton. Traditional approaches to up-conversion, such as nonlinear two-photon absorption (2PA) or triplet fusion, suffer from low efficiency at solar light intensities, a narrow absorption bandwidth, nonoptimal absorption energies, and difficulties for implementing in practical devices.
View Article and Find Full Text PDFJ Phys Chem Lett
July 2015
§Schulich Faculty of Chemistry, Solid State Institute, Russell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa 3200025, Israel.
Lead chalcogenide colloidal quantum dots are attractive candidates for applications operating in the near infrared spectral range. However, their function is forestalled by limited stability under ambient conditions. Prolonged temperature-activated cation-exchange of Cd(2+) for Pb(2+) forms PbSe/CdSe core/shell heterostructures, unveiling a promising surface passivation route and a method to modify the dots' electronic properties.
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