Long term stability of a poled side-chain nonlinear optical polymer

1998 ◽  
Vol 72 (5) ◽  
pp. 540-541 ◽  
Author(s):  
Hong-Tai Man ◽  
Hyun Nam Yoon
1993 ◽  
Vol 328 ◽  
Author(s):  
C. Xu ◽  
B. Wu ◽  
L. R. Dalton ◽  
Y. Shi ◽  
P. M. Ranon ◽  
...  

ABSTRACTWe have developed a novel class of double-end crosslinkable (DEC) chromophores. Processible side-chain nonlinear optical (NLO) polymers with crosslinkable groups at the ends of chromophore pendants were synthesized from DEC Monomers. The polymers were processed into good quality films, which were subsequently poled with a corona setup and thermally cured to attain stable noncentrosymmetric order. Using this DEC approach, we have realized large optical nonlinearities (χ(2) = 90–220 pm/V) with long term stability at 125 °C.


1993 ◽  
Author(s):  
Yongqiang Shi ◽  
Peter M. Ranon ◽  
William H. Steier ◽  
Chengzeng Xu ◽  
Bo Wu ◽  
...  

1996 ◽  
Vol 446 ◽  
Author(s):  
Z. -Y. Cheng ◽  
R. S. Katiyar ◽  
S. Bauer ◽  
S. Bauer-Gogonea

AbstractAmorphous thin films of a typical side-chain nonlinear optical polymer were investigated by means of dielectric spectroscopy and thermally stimulated depolarization current (TSDC) within the temperature range -40°C to 230°C. Three distinct relaxation processes, labelled α, β and γ were observed. The α-relaxation, associated with the glass transition, is well described by the Vogel-Fulcher relation, while the sub glass transition β and γ-relaxation follow Arrhenius relations. The advantage of TSDC over dielectric spectroscopy is demonstrated for the investigation of the weak β-relaxation in the side-chain polymer. Furthermore, the β -relaxation is responsible for the initial, fast decay of the electro-optical response of the side-chain polymer at room temperature.


1995 ◽  
Vol 413 ◽  
Author(s):  
M. H. Lee ◽  
H. J. Lee ◽  
S. G. Han ◽  
H. -Y. Kim ◽  
Y. H. Won

ABSTRACTThe photobleaching mechanism of nonlinear optical polymers has been investigated; the PMMA based polymers with nonlinear optical chromophores, 4-dimethylamino-4'-nitro-stilbene (DANS), 4-dimethylamino-4'-hexylsulfone-stilbene (DASS), and 4'-(2-hexyloxyethyl) ethyl amino-4-nitro azobenzene (DR-16). The photobleaching was carried out using near-UV lines. FTIR spectra and UV-VIS absorption spectra were obtained after each photobleaching. Refractive indices were measured in the photobleaching processes. The results suggest that the photobleaching mechanism of two PMMA based side-chain polymers with DANS and DASS chromophores results from the photo-oxidation and that of the PMMA based host-guest polymer with DR-16 chromophore results from the combination of the photo-degradation and the trans-cis conformational transformation.


2005 ◽  
Author(s):  
Diyun Huang ◽  
Timothy Parker ◽  
Hann Wen Guan ◽  
Shuxin Cong ◽  
Danliang Jin ◽  
...  

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