2011
DOI: 10.1002/adma.201100436
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Organic Photorefractive Materials and Applications

Abstract: This review describes recent advances and applications in the field of organic photorefractive materials, an interesting area in the field of organic electronics and promising candidate for various aspects of photonic applications. We describe the current state of knowledge about the processes involved in the formation of photorefractive gratings in organic materials and focus on the chemical and photo‐physical aspects of the material structures employed in low glass‐transition temperature amorphous composites… Show more

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Cited by 115 publications
(81 citation statements)
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References 242 publications
(319 reference statements)
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“…15. It should be remarked, that at present time different scientific groups have studied the organic photorefractive materials and have found the extended area of their application in the technique and biomedicine [18], [19]. But, it should be mentioned, that basically the authors have drawn the attention on the structuring process influence on the volume of the organics.…”
Section: Resultsmentioning
confidence: 96%
“…15. It should be remarked, that at present time different scientific groups have studied the organic photorefractive materials and have found the extended area of their application in the technique and biomedicine [18], [19]. But, it should be mentioned, that basically the authors have drawn the attention on the structuring process influence on the volume of the organics.…”
Section: Resultsmentioning
confidence: 96%
“…86 Polarizability anisotropy Δα, the ground-state dipole moment μ and the first hyperpolarizability β are significantly affected by structural modifications due to changes in the electron-donating and -accepting substituent groups. The two terms of FOM of the NLO chromophores with various π-conjugated structures with different electron-donating and -accepting substituent groups were individually evaluated as a function of the resonance parameter c 2 for two basic resonance states of push-pull chromophores, a neutral polyene limit (D-A, c 2 = 0), cyanine limit with c 2 = 0.5, zwitterionic limit (betaine type, D + -A − , c 2 = 1) 26,86,87 and as a function of π-bond-order alternations (BOAs). 27,88,89 For π-conjugated molecules with single-double bond series, bondlength alternation (BLA) is defined in terms of the difference between the average lengths of single bonds and that of double bonds, which is significantly related to the optimized geometries.…”
Section: Nlo Dyesmentioning
confidence: 99%
“…Namely, the contribution of the hyperpolarizability term due to the electro-optic effect (Pockels effect) was far outweighed by the contribution of the linear polarization term due to the birefringence of the NLO molecule by the space-charge field (molecular orientation enhancement). 26,27,[86][87][88][89] Beyond the cyanine limit (c 2 40.5, BOA40), some problems have been noted: 26,87 high-melting crystalline solids are generated, which lead to difficulties of dissolving the materials in rather non-polar polymeric matrices. Then, the molecular design around cyanine limits offers better NLO chromophores for enhanced PR performance.…”
Section: Nlo Dyesmentioning
confidence: 99%
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