scholarly journals Erratum: “Analysis of thermal band gap variations of PbS quantum dots by Fourier transform transmission and emission spectroscopy” [Appl. Phys. Lett. 99, 081901 (2011)]

2011 ◽  
Vol 99 (18) ◽  
pp. 189902 ◽  
Author(s):  
B. Ullrich ◽  
J. S. Wang ◽  
G. J. Brown
2006 ◽  
Vol 352 (32-35) ◽  
pp. 3633-3635 ◽  
Author(s):  
P.M. Naves ◽  
T.N. Gonzaga ◽  
A.F.G. Monte ◽  
N.O. Dantas

2019 ◽  
Vol 6 (11) ◽  
pp. 115908 ◽  
Author(s):  
Yun Zhao ◽  
Wei Li

2013 ◽  
Vol 1 (28) ◽  
pp. 4350
Author(s):  
Aurel Diacon ◽  
Edina Rusen ◽  
Alexandra Mocanu ◽  
Leona Cristina Nistor

2019 ◽  
Vol 10 (18) ◽  
pp. 4750-4760 ◽  
Author(s):  
Naoyuki Nishimura ◽  
Jesse R. Allardice ◽  
James Xiao ◽  
Qifei Gu ◽  
Victor Gray ◽  
...  

Photon upconversion with an excitation of energy below the band gap of crystalline silicon was demonstrated with a hybrid system consisting of molecules based on a thiophene conjugated acene (i.e., TES-ADT) and lead sulphide (PbS) quantum dots.


2013 ◽  
Vol 1436 ◽  
Author(s):  
Bruno Ullrich ◽  
Andrew R. Markelonis ◽  
Joanna S. Wang ◽  
Gail J. Brown

ABSTRACTCentrifuge enforced precipitation was used to disperse PbS quantum dots (diameter 4.7 nm) on polyethylene terephthalate. By employing double frequency Fourier transform spectroscopy, we studied the emission properties of the sample. Gaussian shaped emission spectra from cryogenic temperatures up to room temperatures were observed, demonstrating the potential of PbS quantum dots to be used as light emitters in combination with organic matrices. One interesting feature is that the linewidth of the emission spectrum does not follow the expected thermal broadening.


2020 ◽  
Author(s):  
Iván Mora-Seró ◽  
Sofia Masi ◽  
David Macias-Pinilla ◽  
Carlos Echeverría-Arrondo ◽  
Juan Ignacio Climente

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 419
Author(s):  
Saradh Prasad ◽  
Mamduh J. Aljaafreh ◽  
Mohamad S. AlSalhi ◽  
Abeer Alshammari

The notable photophysical characteristics of perovskite quantum dots (PQDs) (CsPbBr3) are suitable for optoelectronic devices. However, the performance of PQDs is unstable because of their surface defects. One way to address the instability is to passivate PQDs using different organic (polymers, oligomers, and dendrimers) or inorganic (ZnS, PbS) materials. In this study, we performed steady-state spectroscopic investigations to measure the photoluminescence (PL), absorption (A), transmission (T), and reflectance (R) of perovskite quantum dots (CsPbBr3) and ethylene vinyl acetate/terpene phenol (1%) (EVA-TPR (1%), or EVA) copolymer/perovskite composites in thin films with a thickness of 352 ± 5 nm. EVA is highly transparent because of its large band gap; furthermore, it is inexpensive and easy to process. However, the compatibility between PQDs and EVA should be established; therefore, a series of analyses was performed to compute parameters, such as the band gap, the coefficients of absorbance and extinction, the index of refractivity, and the dielectric constant (real and imaginary parts), from the data obtained from the above investigation. Finally, the optical conductivities of the films were studied. All these analyses showed that the EVA/PQDs were more efficient and stable both physically and optically. Hence, EVA/PQDs could become copolymer/perovskite active materials suitable for optoelectronic devices, such as solar cells and perovskite/polymer light-emitting diodes (PPLEDs).


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Tamara Sloboda ◽  
Sebastian Svanström ◽  
Fredrik O. L. Johansson ◽  
Aneta Andruszkiewicz ◽  
Xiaoliang Zhang ◽  
...  

AbstractTime-resolved photoelectron spectroscopy can give insights into carrier dynamics and offers the possibility of element and site-specific information through the measurements of core levels. In this paper, we demonstrate that this method can access electrons dynamics in PbS quantum dots over a wide time window spanning from pico- to microseconds in a single experiment carried out at the synchrotron facility BESSY II. The method is sensitive to small changes in core level positions. Fast measurements at low pump fluences are enabled by the use of a pump laser at a lower repetition frequency than the repetition frequency of the X-ray pulses used to probe the core level electrons: Through the use of a time-resolved spectrometer, time-dependent analysis of data from all synchrotron pulses is possible. Furthermore, by picosecond control of the pump laser arrival at the sample relative to the X-ray pulses, a time-resolution limited only by the length of the X-ray pulses is achieved. Using this method, we studied the charge dynamics in thin film samples of PbS quantum dots on n-type MgZnO substrates through time-resolved measurements of the Pb 5d core level. We found a time-resolved core level shift, which we could assign to electron injection and charge accumulation at the MgZnO/PbS quantum dots interface. This assignment was confirmed through the measurement of PbS films with different thicknesses. Our results therefore give insight into the magnitude of the photovoltage generated specifically at the MgZnO/PbS interface and into the timescale of charge transport and electron injection, as well as into the timescale of charge recombination at this interface. It is a unique feature of our method that the timescale of both these processes can be accessed in a single experiment and investigated for a specific interface.


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