The effect of external applied fields on the third order nonlinear susceptibility and two-photon absorption cross-section of E5CN7@Fe3O4-CNT

2019 ◽  
Vol 119 ◽  
pp. 105653 ◽  
Author(s):  
M.H. Majles Ara ◽  
Z. Dehghani ◽  
M. Nadafan
2009 ◽  
Vol 18 (01) ◽  
pp. 161-166 ◽  
Author(s):  
ALEJANDRA ORTEGA ◽  
ANA LAURA PEREZ-MARTINEZ ◽  
TAKESHI OGAWA ◽  
FRANCIS SMITH ◽  
ARDIE WALSER ◽  
...  

A highly-conjugated polar dye with three aromatic rings connected with azo groups was prepared and it was incorporated in polycinnamate. It showed a third-order nonlinear susceptibility of 8 × 10-10 esu determined by a Z-scan technique. The unpoled and poled films show the same susceptibility indicating the polymer film could not be poled. The open aperture Z-scan showed negligible two-photon absorption at 1064 nm.


2004 ◽  
Vol 13 (03n04) ◽  
pp. 461-466 ◽  
Author(s):  
MARK G. KUZYK

Ever since researchers first probed materials with light, a natural question they have asked pertains to the strength of this interaction. Can materials be made to more strongly absorb light at certain wavelengths, thereby yielding vibrant colors? Can the nonlinear interaction between two beams be used to make an optical switching device? How efficiently can we convert the frequency of light through a nonlinear interaction? All of these questions, in effect, are the same. Equivalently, the question can be phrased as, "how large can we make the linear or the nonlinear susceptibility?" In this paper, we apply sum rules to calculate the maximum limit of the doubly resonant two-photon absorption cross-section. We find that even for a single electron system, the cross-section can exceed δ=105 GM .


2007 ◽  
Vol 11 (06) ◽  
pp. 406-417 ◽  
Author(s):  
Yusuke Inaba ◽  
Kazuya Ogawa ◽  
Yoshiaki Kobuke

Acetylene-bridged bisporphyrins and trisporphyrins having branched bulky bis(carboxylethyl)methyl meso-substituents were synthesized. These compounds showed large effective two-photon absorption cross-section values at 890 nm measured by using a nanosecond Z-scan method. Sodium salt of hydrolyzed trisporphyrins showed broad and red-shifted Q-bands over 900 nm. Two-photon absorption cross-section values of water-soluble dimers in water were similar to, or slightly larger than, those of ester forms evaluated in toluene. Furthermore, the generation of singlet oxygen upon one-photon irradiation for dimers in water was confirmed.


2018 ◽  
Vol 42 (17) ◽  
pp. 14325-14331 ◽  
Author(s):  
Ruiqing Feng ◽  
Longlong Li ◽  
Bing Li ◽  
Jinhui Li ◽  
Dan Peng ◽  
...  

DMI could light up the RNA of the nucleus and the cytoplasm in living systems, which not only exhibits larger two-photon absorption cross-sections (981 GM), but also displays high-permeability to plasma membranes of vigorous cells.


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.


Sign in / Sign up

Export Citation Format

Share Document