scholarly journals Mechanisms of fluorescence decays of colloidal CdSe–CdS/ZnS quantum dots unraveled by time-resolved fluorescence measurement

2015 ◽  
Vol 17 (41) ◽  
pp. 27588-27595 ◽  
Author(s):  
Hao Xu ◽  
Volodymyr Chmyrov ◽  
Jerker Widengren ◽  
Hjalmar Brismar ◽  
Ying Fu

The fluorescence decay spectrum of colloidal CdSe-based quantum dots is characterized by energy relaxation and radiative recombination of photoexcited excitons.

1990 ◽  
Vol 68 (9) ◽  
pp. 1013-1022 ◽  
Author(s):  
Naoto Tamai ◽  
Tomoko Yamazaki ◽  
Iwao Yamazaki

Fluorescence-decay curves and time-resolved fluorescence spectra of N, N′-dioctadecylrhodamine B in Langmuir–Blodgett monolayers have been measured by means of a picosecond time-resolved fluorescence spectrophotometer. The excitation energy relaxation of the dye molecule in the monolayers was compared at 295 and 80 K in the concentration range from 0.02 to 31 mol%. The relaxation of the dynamic Stokes shift was found to decay logarithmically with time in longer time regions when the concentration of N, N′-dioctadecylrhodamine B < 5 mol%. The fluorescence decays can be analyzed by an equation including a stretched exponential function. The mechanisms of singlet excitation-energy relaxation were interpreted in terms of (i) the energy migration among energetically disordered monomer sites represented by ultrametric space (hierarchical energy distribution) or the Gaussian distribution of the density of excited states and (ii) the energy trapping by two-dimensional aggregates. It was found that the relaxation of the dynamic Stokes shift and the fluorescence decay can be estimated by the diffusion length of the excitation-energy transport.


2014 ◽  
Vol 289 (39) ◽  
pp. 26817-26828 ◽  
Author(s):  
Christoph Röthlein ◽  
Markus S. Miettinen ◽  
Tejas Borwankar ◽  
Jörg Bürger ◽  
Thorsten Mielke ◽  
...  

2020 ◽  
Vol 10 (3) ◽  
pp. 178-188
Author(s):  
Bipin Rooj ◽  
Ankita Dutta ◽  
Debojyoti Mukherjee ◽  
Sahidul Islam ◽  
Ujjwal Mandal

Background: Understanding the interaction between different organic dyes and carbon quantum dots helps us to understand several photo physical processes like electron transfer, energy transfer, molecular sensing, drug delivery and dye degradation processes etc. Objective: The primary objective of this study is to whether the carbon quantum dots can act as an electron donor and can participate in the different photo physical processes. Methods: In this work, Carbon Quantum Dots (CQDLs) are synthesized in most economical and simple carbonization method where petals of Nelumbo nucifera L. are used as a carbon precursor. The synthesized CQDLs were characterized by using experimental techniques like UV−Vis absorption, FT-IR, Transmission Electron Microscopy (TEM), steadystate and time-resolved fluorescence spectroscopy. Results: The spectral analysis shows that the so synthesized CQDLs are spherical in shape and its diameter is around 4.2 nm. It shows the fluorescence emission maximum at 495 nm with a quantum yield of 4%. In this work the interaction between Carbon Quantum Dots (CQDLs) and an organic dye Malachite Green (MG) is studied using fluorescence spectroscopic technique under ambient pH condition (At pH 7). The quenching mechanism of CQDLs with MG was investigated using Stern-Volmer equation and time-resolved fluorescence lifetime studies. The results show that the dominant process of fluorescence quenching is attributed to Forster Resonance Energy Transfer (FRET) having a donor acceptor distance of 53 Å where CQDLs act as a donor and MG acts as an acceptor. Conclusion: This work has a consequence that CQDLs can be used as a donor species for different photo physical processes such as photovoltaic cell, dye sensitized solar cell, and also for antioxidant activity study.


2017 ◽  
Vol 468 ◽  
pp. 300-307 ◽  
Author(s):  
Gregory E. LeCroy ◽  
K.A. Shiral Fernando ◽  
Christopher E. Bunker ◽  
Ping Wang ◽  
Nicholas Tomlinson ◽  
...  

1991 ◽  
Vol 20 (5) ◽  
pp. 247-262 ◽  
Author(s):  
?eljko Bajzer ◽  
Terry M. Therneau ◽  
Joseph C. Sharp ◽  
Franklin G. Prendergast

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