Features of the influence of stabilizing ligands on luminescence properties of cadmium selenide colloidal quantum dots

2017 ◽  
Vol 51 (1) ◽  
pp. 38-45 ◽  
Author(s):  
M. G. Spirin ◽  
S. B. Brichkin ◽  
V. F. Razumov
2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Lifeng Wang ◽  
Zongwei Chen ◽  
Guijie Liang ◽  
Yulu Li ◽  
Runchen Lai ◽  
...  

Abstract Hot electrons can dramatically improve the efficiency of solar cells and sensitize energetically-demanding photochemical reactions. Efficient hot electron devices have been hindered by sub-picosecond intraband cooling of hot electrons in typical semiconductors via electron-phonon scattering. Semiconductor quantum dots were predicted to exhibit a “phonon bottleneck” for hot electron relaxation as their quantum-confined electrons would couple very inefficiently to phonons. However, typical cadmium selenide dots still exhibit sub-picosecond hot electron cooling, bypassing the phonon bottleneck possibly via an Auger-like process whereby the excessive energy of the hot electron is transferred to the hole. Here we demonstrate this cooling mechanism can be suppressed in copper-doped cadmium selenide colloidal quantum dots due to femtosecond hole capturing by copper-dopants. As a result, we observe a lifetime of ~8.6 picosecond for 1Pe hot electrons which is more than 30-fold longer than that in same-sized, undoped dots (~0.25 picosecond).


2014 ◽  
Vol 572 ◽  
pp. 012028 ◽  
Author(s):  
D S Mazing ◽  
L B Matyushkin ◽  
O A Aleksandrova ◽  
I I Mikhailov ◽  
V A Moshnikov ◽  
...  

2015 ◽  
Vol 661 ◽  
pp. 012033 ◽  
Author(s):  
D S Mazing ◽  
A M Brovko ◽  
L B Matyushkin ◽  
O A Aleksandrova ◽  
V A Moshnikov

2015 ◽  
Vol 643 ◽  
pp. 012080 ◽  
Author(s):  
I I Mikhailov ◽  
S A Tarasov ◽  
I I Lamkin ◽  
M Y Andreev ◽  
A V Solomonov

2008 ◽  
Vol 1133 ◽  
Author(s):  
Subhasish Chatterjee ◽  
Nikesh V. Valappil ◽  
Vinod M. Menon

Abstract Quantum dots play a promising role in the development of novel optical and biosensing devices. In this study, we investigated steady state and time-dependent luminescence properties of InGaP/ZnS core/shell colloidal quantum dots in a solution phase at room temperature. The steady state experiments exhibited an emission maximum at 650 nm with full width at half maximum of ~ 85 nm, and strong first-excitonic absorption peak at 600 nm. The time-resolved luminescence measurements depicted a bi-exponential decay profile with lifetimes of τ1 ~ 47 ns and τ2 ~ 142 ns at the emission maximum. Additionally, luminescence quenching and lifetime reduction due to resonance energy transfer between the quantum dot and an absorber are demonstrated. Our results support the plausibility of using these InGaP quantum dots as an effective alternative to highly toxic conventional Cd or Pb based colloidal quantum dots for biological applications.


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