The nonlinear optical properties of organics with unsaturated bonds were compared with those of inorganics including semiconductors and dielectrics. Because of the mesomeric effect, namely quantum mechanical resonance effect among configurations, aromatic molecules and polymers have larger optical nonlinear parameters defined as δ(n)=X(n)/(X(l))n both for the second (n=2) and third-order (n=3) nonlinearities. Experimental results of ultrafast nonlinear response of conjugated polymers, especially polydiacetylenes, were described and a model is proposed to explain the relaxation processes of photoexcitations in the conjugated polymers. Applying the model constructed on the basis of the extensive experimental study, we propose model polymers to obtain ultrafast resonant optical nonlinearity.
The copyright of the original papers published on this site belongs to IEICE. Unauthorized use of the original or translated papers is prohibited. See IEICE Provisions on Copyright for details.
Copy
Takayoshi KOBAYASHI, "Nonlinear Optical Properties of Organics in Comparison with Semiconductors and Dielectrics" in IEICE TRANSACTIONS on Fundamentals,
vol. E75-A, no. 1, pp. 38-45, January 1992, doi: .
Abstract: The nonlinear optical properties of organics with unsaturated bonds were compared with those of inorganics including semiconductors and dielectrics. Because of the mesomeric effect, namely quantum mechanical resonance effect among configurations, aromatic molecules and polymers have larger optical nonlinear parameters defined as δ(n)=X(n)/(X(l))n both for the second (n=2) and third-order (n=3) nonlinearities. Experimental results of ultrafast nonlinear response of conjugated polymers, especially polydiacetylenes, were described and a model is proposed to explain the relaxation processes of photoexcitations in the conjugated polymers. Applying the model constructed on the basis of the extensive experimental study, we propose model polymers to obtain ultrafast resonant optical nonlinearity.
URL: https://globals.ieice.org/en_transactions/fundamentals/10.1587/e75-a_1_38/_p
Copy
@ARTICLE{e75-a_1_38,
author={Takayoshi KOBAYASHI, },
journal={IEICE TRANSACTIONS on Fundamentals},
title={Nonlinear Optical Properties of Organics in Comparison with Semiconductors and Dielectrics},
year={1992},
volume={E75-A},
number={1},
pages={38-45},
abstract={The nonlinear optical properties of organics with unsaturated bonds were compared with those of inorganics including semiconductors and dielectrics. Because of the mesomeric effect, namely quantum mechanical resonance effect among configurations, aromatic molecules and polymers have larger optical nonlinear parameters defined as δ(n)=X(n)/(X(l))n both for the second (n=2) and third-order (n=3) nonlinearities. Experimental results of ultrafast nonlinear response of conjugated polymers, especially polydiacetylenes, were described and a model is proposed to explain the relaxation processes of photoexcitations in the conjugated polymers. Applying the model constructed on the basis of the extensive experimental study, we propose model polymers to obtain ultrafast resonant optical nonlinearity.},
keywords={},
doi={},
ISSN={},
month={January},}
Copy
TY - JOUR
TI - Nonlinear Optical Properties of Organics in Comparison with Semiconductors and Dielectrics
T2 - IEICE TRANSACTIONS on Fundamentals
SP - 38
EP - 45
AU - Takayoshi KOBAYASHI
PY - 1992
DO -
JO - IEICE TRANSACTIONS on Fundamentals
SN -
VL - E75-A
IS - 1
JA - IEICE TRANSACTIONS on Fundamentals
Y1 - January 1992
AB - The nonlinear optical properties of organics with unsaturated bonds were compared with those of inorganics including semiconductors and dielectrics. Because of the mesomeric effect, namely quantum mechanical resonance effect among configurations, aromatic molecules and polymers have larger optical nonlinear parameters defined as δ(n)=X(n)/(X(l))n both for the second (n=2) and third-order (n=3) nonlinearities. Experimental results of ultrafast nonlinear response of conjugated polymers, especially polydiacetylenes, were described and a model is proposed to explain the relaxation processes of photoexcitations in the conjugated polymers. Applying the model constructed on the basis of the extensive experimental study, we propose model polymers to obtain ultrafast resonant optical nonlinearity.
ER -