Abstract:Carrier trapping in organic photorefractive (PR) composites is affected by the bulk state (which can be varied by modifying the molecule structure and processing method used) and the presence of dipolar molecules. Such situations complicate the understanding of carrier trapping in PR composites. The density of states (DOS) provides direct information about carrier trapping in materials. Here, the first attempt to directly measure the DOS in PR composites is performed to investigate the effect of the change of … Show more
“…Organic photorefractive (PR) polymers have wide potential for updatable holographic imaging and dynamic holographic displays. Dynamic holography is the ultimate in three-dimensional (3D) imaging and is expected to be key technology for a next-generation display system. − Photorefractive phenomena are based on refractive index modulation derived from the distributed space-charge field through the Pockels (first-order optical nonlinearity) effect. − Since the first study of organic photorefractive polymers was reported, numerous research investigations have focused on PR polymers. − ,− …”
The objective of the present study is to demonstrate and evaluate the photorefractive (PR) performance of an all-organic PR device with a self-assembled monolayer (SAM)-modified organic conductive electrode of PEDOT:PSS coated on polyethylene terephthalate (PET). The PR composite consisted of a triphenylamine-based photoconductive polymer: poly(4-(diphenylamino)benzyl acrylate) (PDAA), a triphenylamine photoconductive plasticizer: (4-(diphenylamino)phenyl)methanol (TPAOH), a nonlinear optical dye based on aminocyanostyrene: (4asacycloheptylbenzylidenemalononitrile) (7-DCST), and soluble fullerene: [6,6]-phenyl C 61 butyric acid-methyl ester (PCBM). For comparison with the all-organic PR device, the PR performances using PET/ITO, glass/ITO, and glass/PEDOT:PSS substrates were also evaluated. At an applied electric field of 40 V μm −1 , the diffraction efficiency and the response time of the PR device using the PET/PEDOT:PSS-SAM substrate were 21.9%, and 390 ms, respectively. As a result of repeating bending tests on this all-organic PR device, we found that the flexible PR device with the PET/PEDOT:PSS-SAM substrate had a potential to withstand bending 10 000 times and that the change in the haze value strongly influenced the degradation of PR performance.
“…Organic photorefractive (PR) polymers have wide potential for updatable holographic imaging and dynamic holographic displays. Dynamic holography is the ultimate in three-dimensional (3D) imaging and is expected to be key technology for a next-generation display system. − Photorefractive phenomena are based on refractive index modulation derived from the distributed space-charge field through the Pockels (first-order optical nonlinearity) effect. − Since the first study of organic photorefractive polymers was reported, numerous research investigations have focused on PR polymers. − ,− …”
The objective of the present study is to demonstrate and evaluate the photorefractive (PR) performance of an all-organic PR device with a self-assembled monolayer (SAM)-modified organic conductive electrode of PEDOT:PSS coated on polyethylene terephthalate (PET). The PR composite consisted of a triphenylamine-based photoconductive polymer: poly(4-(diphenylamino)benzyl acrylate) (PDAA), a triphenylamine photoconductive plasticizer: (4-(diphenylamino)phenyl)methanol (TPAOH), a nonlinear optical dye based on aminocyanostyrene: (4asacycloheptylbenzylidenemalononitrile) (7-DCST), and soluble fullerene: [6,6]-phenyl C 61 butyric acid-methyl ester (PCBM). For comparison with the all-organic PR device, the PR performances using PET/ITO, glass/ITO, and glass/PEDOT:PSS substrates were also evaluated. At an applied electric field of 40 V μm −1 , the diffraction efficiency and the response time of the PR device using the PET/PEDOT:PSS-SAM substrate were 21.9%, and 390 ms, respectively. As a result of repeating bending tests on this all-organic PR device, we found that the flexible PR device with the PET/PEDOT:PSS-SAM substrate had a potential to withstand bending 10 000 times and that the change in the haze value strongly influenced the degradation of PR performance.
“…Among various organic PR materials, gust-host systems, prepared by doping small molecular NLO chromophores into polymeric photoconductors, are the most studied for practical application because of their eases of fabrication. [7,8] However, with the increasing of NLO chromophore doping concentration, the unfavorable antiparallel packing of chromophores resulting from the strong interchromophore dipole-dipole interactions gradually appeared, leading to a decreased PR effect. [9] Recently, some nonlinear molecules such as hyper-structured molecules (HSMs), [10] star-shaped molecules, [11] dendritic molecules, [12] etc.…”
Seven C-methylcalix[4]resorcinarene (CRA)-based photorefractive (PR) hyper-structured molecular glasses (HSMGs) containing carbazole-based methine nonlinear optical (NLO) chromophores were designed and synthesized via esterification between carboxyl-containing asymmetric CRA core molecule and hydroxyl-containing functional compounds. When the feed ratio of hydroxyl-containing NLO functional compounds to carboxyl groups of CRA-COOH was kept at 1.5/1 by mole, the degree of introduction of NLO chromophore to the CRA core was above 70%. All the HSMGs show low glass transition temperatures (Tg), and good solubility in common low boiling point solvents such as THF, CHCl3, etc. Powder XRD and UV-vis absorption in films of HSMGs indicate that the aggregation, packing and crystallization of the NLO chromophores in these HSMGs had been effectively reduced. Doping with Nethyl-carbazole (ECz) as a plasticizer and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) as a photosensitizer, all the HSMGs composites showed good PR effects. All the coupling gain coefficients (Γ) of HSMGs-based composites are about twice to the corresponding small molecular NLO chromophores-based composites, thanks to the decreased NLO chromophores antiparallel packing caused by the asymmetric CRA core. Among them, CRA-CSN/ECz/PCBM (69:30:1, wt.%) composite exhibited the best performance with the Γ value of 78.2 cm-1 at the external electric field of 12.5 V μm-1 , which is one of the best performance in molecular glasses under the same test conditions. Coupled with their convenient synthesis, this work will provide a new simple design strategy for organic PR materials.
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