WITHDRAWN: Third order nonlinear optical effects in copper phthalocyanines (CuPc) using DFWM and THG techniques

2006 ◽  
Author(s):  
B. Derkowska ◽  
M. Wojdyła ◽  
P. Rytlewski ◽  
R. Czaplicki ◽  
Z. Sofiani ◽  
...  
Keyword(s):  
Nonlinear Optical ◽  
Third Order ◽  
Optical Effects ◽  
Nonlinear Optical Effects ◽  
Copper Phthalocyanines

Magneto-conductive encryption assisted by third-order nonlinear optical effects in carbon/metal nanohybrids

2017 ◽  
Vol 4 (3) ◽  
pp. 035601 ◽  
Author(s):  
J A García-Merino ◽  
C Mercado-Zúñiga ◽  
C L Martínez-González ◽  
C R Torres-SanMiguel ◽  
J R Vargas-García ◽  
...  
Keyword(s):  
Nonlinear Optical ◽  
Third Order ◽  
Optical Effects ◽  
Nonlinear Optical Effects

Research progress of third-order nonlinear optical effects excited by vectorial light fields （Invited）

2020 ◽  
Vol 49 (12) ◽  
pp. 20201050-20201050
Author(s):  
顾兵 Bing Gu ◽  
胡月球 Yueqiu Hu ◽  
闻博 Bo Wen
Keyword(s):  
Nonlinear Optical ◽  
Research Progress ◽  
Light Fields ◽  
Third Order ◽  
Optical Effects ◽  
Nonlinear Optical Effects

ChemInform Abstract: Optical Limiting Behavior of Nanosized Polyicosahedral Gold-Silver Clusters Based on Third-Order Nonlinear Optical Effects.

ChemInform ◽  
2010 ◽  
Vol 33 (5) ◽  
pp. no-no
Author(s):  
Hong Zhang ◽  
David E. Zelmon ◽  
Luogen Deng ◽  
Hua-Kuang Liu ◽  
Boon K. Teo
Keyword(s):  
Nonlinear Optical ◽  
Optical Limiting ◽  
Silver Clusters ◽  
Third Order ◽  
Limiting Behavior ◽  
Gold Silver ◽  
Optical Effects ◽  
Nonlinear Optical Effects

Third Order Nonlinear Optical Effects in Conjugated Polymers and DYE Systems

1991 ◽  
pp. 335-343 ◽  
Author(s):  
C. Bubeck ◽  
A. Grund ◽  
A. Kaltbeitzel ◽  
D. Neher ◽  
A. Mathy ◽  
...  
Keyword(s):  
Conjugated Polymers ◽  
Nonlinear Optical ◽  
Third Order ◽  
Optical Effects ◽  
Nonlinear Optical Effects

Z-scan evaluation of the third-order nonlinear-optical effects of organic single crystals

2003 ◽  
Author(s):  
T. Iwamura ◽  
T. Aihara ◽  
S. Umegaki ◽  
H. Adachi ◽  
K. Nagaoka ◽  
...  
Keyword(s):  
Single Crystals ◽  
Nonlinear Optical ◽  
Third Order ◽  
The Third ◽  
Optical Effects ◽  
Nonlinear Optical Effects

NONLINEAR OPTICAL RESPONSE OF C60 AND C70 FULLERENES

1992 ◽  
Vol 06 (22) ◽  
pp. 1351-1360 ◽  
Author(s):  
W. J. BLAU ◽  
D. J. CARDIN
Keyword(s):  
Nonlinear Optical ◽  
Chemical Properties ◽  
Optical Response ◽  
Nonlinear Optical Response ◽  
Physical And Chemical Properties ◽  
Third Order ◽  
Optical Effects ◽  
Nonlinear Optical Effects ◽  
Physical And Chemical ◽  
And Chemical Properties

The macroscopic preparation of novel conjugated allotropes of carbon, the Fullerenes, has become easy to achieve and commonplace, leading to widespread study of their physical and chemical properties. In this paper we review the nonlinear optical effects observed in Fullerenes to date. Both second and third order response has been studied and the results indicate that this class of materials is highly promising for optoelectronic applications.

Optical Limiting Behavior of Nanosized Polyicosahedral Gold−Silver Clusters Based on Third-Order Nonlinear Optical Effects

2001 ◽  
Vol 123 (45) ◽  
pp. 11300-11301 ◽  
Author(s):  
Hong Zhang ◽  
David E. Zelmon ◽  
Luogen Deng ◽  
Hua-Kuang Liu ◽  
Boon K. Teo
Keyword(s):  
Nonlinear Optical ◽  
Optical Limiting ◽  
Silver Clusters ◽  
Third Order ◽  
Limiting Behavior ◽  
Gold Silver ◽  
Optical Effects ◽  
Nonlinear Optical Effects

scholarly journals Nonlinear Optical Effects in Polymeric Azoesters

2010 ◽  
Vol 4 (3) ◽  
pp. 185-190
Author(s):  
Oksana Nadtoka ◽  
Keyword(s):  
Nonlinear Optical ◽  
Electronic Effect ◽  
Wave Mixing ◽  
Third Order ◽  
The Third ◽  
Nlo Property ◽  
Optical Effects ◽  
Nonlinear Optical Effects ◽  
Chromophore Concentration ◽  
Photochromic Polymers

The new photochromic polymers based on methacrylic azoesters were synthesized. The azobenzene side chains of obtained polymers contain different groups of both acceptor and donor nature as well as flexible alkyl spacer. The third order nonlinear optical susceptibilities (3) of the studied solutions were measured by degenerating four wave mixing (DFWM) method. As a result, the enhancement of the molecular conjugation and the high NLO chromophore concentration in the molecular chain contribute much to heightening the third-order NLO effect. The electronic effect of the substituent on the azobenzol group and the push–pull electronic structure contributes much to enhancing the NLO property

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