Nonlinear Absorption in Organic Dyes

1994 ◽  
Vol 374 ◽  
Author(s):  
K. R. Welford ◽  
S. N. R. Swatton ◽  
S. Hughes ◽  
S. J. Till ◽  
G. Spruce ◽  
...  

AbstractThe non-linear optical properties of chloro-aluminium phthalocyanine and 1,3,3,1′,3′,3′- hexamethylindotricarbocyanine have been studied as model systems using z-scan and time resolved experimental techniques. Excited state lifetimes and absorption cross sections have been measured as well as the spectral response of the induced absorption. Excited state lifetimes are critical in determining the performance of a reverse saturable absorber. Even though a first excited state absorption cross section may be large compared with the ground state absorption cross section the lifetimes and transition probabilities of higher lying states can lead to constraints upon how effective organic dyes are as optical limiting materials.Both novel saturation of the induced absorption at high laser fluences and intermolecular quantum beats in 1,3,3, 1′,3′,3′-hexamethylindotricarbocyanine are demonstrated experimentally and accounted for theoretically. Quantum chemical calculations have been developed to propose a probable inter-molecular mechanism for the observed quantum beats.

2019 ◽  
Vol 15 ◽  
pp. 2438-2446 ◽  
Author(s):  
Alessandro Iagatti ◽  
Baihao Shao ◽  
Alberto Credi ◽  
Barbara Ventura ◽  
Ivan Aprahamian ◽  
...  

In this work we apply a combination of steady state and time resolved luminescence and absorption spectroscopies to investigate the excited-state dynamics of a recently developed molecular photoswitch, belonging to the hydrazone family. The outstanding properties of this molecule, involving fluorescence toggling, bistability, high isomerization quantum yield and non-negligible two-photon absorption cross section, make it very promising for numerous applications. Here we show that the light induced Z/E isomerization occurs on a fast <1 ps timescale in both toluene and acetonitrile, while the excited state lifetime of the Z-form depends on solvent polarity, suggesting a partial charge transfer nature of its low lying excited state. Time-resolved luminescence measurements evidence the presence of a main emission component in the 500–520 nm spectral range, attributed to the Z-isomer, and a very short living blue-shifted emission, attributed to the E-isomer. Finally, transient absorption measurements performed upon far-red excitation are employed as an alternative method to determine the two-photon absorption cross-section of the molecule.


2011 ◽  
Vol 15 (09n10) ◽  
pp. 858-864 ◽  
Author(s):  
Jong Min Lim ◽  
Iti Gupta ◽  
Hiroyuki Furuta ◽  
Dongho Kim

We have investigated the photophysical properties of [22] π-conjugated pentapyrrolic systems, sapphyrin, N-confused and N-fused sapphyrins, with a particular focus on the effects of confused and fused pyrrole rings on their electronic structures using steady-state and time-resolved spectroscopic methods, two-photon absorption cross-section (σ(2)) measurements and quantum mechanical calculations. The absorption spectra of N-confused and N-fused sapphyrins exhibit relatively red-shifted features compared to sapphyrin. In parallel with these spectral features, the reduced HOMO–LUMO gaps were observed in going from sapphyrin to N-fused sapphyrin. In the analysis of the anisotropy of the induced current density (AICD), N-confused and N-fused sapphyrins show that extra π-electrons in confused and fused pyrrole rings contribute to the extension of their π-conjugation pathways. Slightly larger twophoton absorption cross-section values of N-confused and N-fused sapphyrins (3250 and 3900 GM) than that of sapphyrin (2900 GM) also reflect an enhanced π-conjugation effect due to bicyclic and endocyclic extensions in π-conjugation pathways, respectively. The excited singlet and triplet state lifetimes of N-confused sapphyrin were determined to be 60 ps and 1 μs, respectively, due to conformational change and acceleration of nonradiative decay processes, being in a sharp contrast with those of sapphyrin (2.4 ns and 13 μs, respectively). In the case of N-fused sapphyrin, very short singlet excited-state lifetime of 5 ps was detected probably due to the excited-state NH-tautomerization process which enhances nonradiative decay processes.


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