Transient Isoemissive Point Observed in the Temperature-Dependent Fluorescence Decay of J-Aggregates Adsorbed on Silica Gel

1990 ◽  
Vol 19 (10) ◽  
pp. 1785-1788 ◽  
Author(s):  
Klaus Kemnitz ◽  
Keitaro Yoshihara ◽  
Tadaaki Tani
2017 ◽  
Vol 53 (93) ◽  
pp. 12556-12559 ◽  
Author(s):  
Cecilia Cerretani ◽  
Miguel R. Carro-Temboury ◽  
Stefan Krause ◽  
Sidsel Ammitzbøll Bogh ◽  
Tom Vosch

The average fluorescence decay time of DNA-stabilized silver nanoclusters is temperature dependent and could find applications in nanothermometry.


2014 ◽  
Vol 118 (42) ◽  
pp. 24325-24334 ◽  
Author(s):  
Katie A. Clark ◽  
Emma L. Krueger ◽  
David A. Vanden Bout

1996 ◽  
Vol 16 (3) ◽  
pp. 179-196
Author(s):  
H. Glaeske ◽  
K.-H. Feller ◽  
E. Gaišaukas ◽  
L. Knöll

Quantum beats in transient absorption of PIC-J-aggregates, modelled by a modified 3-level-system are calculated. Experimental conditions for the possibility of their observation are investigated. The influence of the temperature dependent phase relaxation on the temporal evolution of quantum beat signals is considered.


1996 ◽  
Vol 100 (21) ◽  
pp. 8640-8644 ◽  
Author(s):  
Valey F. Kamalov ◽  
Irina A. Struganova ◽  
Keitaro Yoshihara

2021 ◽  
Author(s):  
Arundhati Deshmukh ◽  
Niklas Geue ◽  
Nadine Bardbury ◽  
Timothy Atallah ◽  
Chern Chuang ◽  
...  

Molecular aggregates with long-range excitonic couplings have drastically different photophysical properties compared to their monomer counterparts. From Kasha’s model for 1-dimensional systems, positive or negative excitonic couplings lead to blue or red shifted optical spectra with respect to the monomers, labelled H-and J-aggregates respectively. The overall excitonic couplings in higher dimensional systems are much more complicated and cannot be simply classified from their spectral shifts alone. Here, we provide a unified classification for extended 2D aggregates using temperature dependent peak shifts, thermal broadening and quantum yields. We discuss the examples of six 2D aggregates with J-like absorption spectra but quite drastic changes quantum yields and superradiance. We find the origin of the differences is, in fact, a different excitonic band structure where the bright state is lower energy than the monomer but still away from the band edge. We call this an ‘I-aggregate’. Our results provide a description of the complex excitonic behaviors that cannot be explained solely on Kasha’s model. Further, such properties can be tuned with the packing geometries within the aggregates providing supramolecular pathways for controlling them. This will allow for precise optimizations of aggregate properties in their applications across the areas of optoelectronics, photonics, excitonic energy transfer, and shortwave infrared technologies.


2021 ◽  
Author(s):  
Arundhati Deshmukh ◽  
Niklas Geue ◽  
Nadine Bradbury ◽  
Timothy Atallah ◽  
Chern Chuang ◽  
...  

Molecular aggregates with long-range excitonic couplings have drastically different photophysical properties compared to their monomer counterparts. From Kasha’s model for 1-dimensional systems, positive or negative excitonic couplings lead to blue or red shifted optical spectra with respect to the monomers, labelled H-and J-aggregates respectively. The overall excitonic couplings in higher dimensional systems are much more complicated and cannot be simply classified from their spectral shifts alone. Here, we provide a unified classification for extended 2D aggregates using temperature dependent peak shifts, thermal broadening and quantum yields. We discuss the examples of six 2D aggregates with J-like absorption spectra but quite drastic changes quantum yields and superradiance. We find the origin of the differences is, in fact, a different excitonic band structure where the bright state is lower energy than the monomer but still away from the band edge. We call this an ‘I-aggregate’. Our results provide a description of the complex excitonic behaviors that cannot be explained solely on Kasha’s model. Further, such properties can be tuned with the packing geometries within the aggregates providing supramolecular pathways for controlling them. This will allow for precise optimizations of aggregate properties in their applications across the areas of optoelectronics, photonics, excitonic energy transfer, and shortwave infrared technologies.


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