Papers by Keyword: Azobenzene Derivatives

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Abstract: A new photochromic ZrO2 precursor solution was prepared using zirconium tetra-n-butoxide, 4-(phenylazo)benzoic acid and ethyleneglycol monomethylether. The density functional theory (DFT) calculation has identified that the structure of the synthesized precursor molecule changed by UV irradiation. The two kinds of thin films were prepared using the photosensitive ZrO2 precursor solution without and with UV irradiation. The surface morphology of thin films changed by UV irradiation. It was found that the surface morphology of thin films is controlled by the difference of precursor structure introduced by UV irradiation.
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Abstract: A new photochromic ZrO2 precursor solution was prepared using zirconium tetra-n-butoxide, 4-(phenylazo)benzoic acid and ethyleneglycol monomethylether. The ZrO2 precursor solution was irradiated with ultraviolet light (UV) at room temperature. After that, UV-irradiated precursor solution was irradiated with visible light (Vis) at room temperature. UV-Vis spectra were measured before irradiation, after UV irradiation and Vis irradiation. Changes of UV-Vis spectra indicated that the new ZrO2 precursor including 4-(phenylazo)benzoic acid shows photochromism. The phenomena have synchronized with reversible photoisomerization of 4-(phenylazo)benzoic acid in the precursor. In addition, the difference of peak position originated from Zr-O CT transition between before UV irradiation and after UV irradiation increased with increasing the concentration of 4-(phenylazo)benzoic acid. Furthermore, the optimized structure of the new ZrO2 precursor was derived by density functional theory (DFT) calculation.
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Abstract: The UV-Vis absorption spectrum of ZrO2 precursor solution containing 4-(phenylazo)benzoic acid (C6H5N=NC6H4COOH) reversibly changed accompanied with reversible change of the spectrum of 4-(phenylazo)benzoic acid by light irradiation. However, the spectrum of ZrO2 precursor solution containing azobenzene (C6H5N=NC6H5) did not change accompanied with reversible change of azobenzene by light irradiation. Furthermore, the back reaction of ZrO2 precursor solution containing 4-(phenylazo)benzoic acid by visible light irradiation was suppressed even if the back reaction of 4-(phenylazo)benzoic acid has occurred by visible light irradiation, when the hydrolysis of ZrO2 precursor was suitably controlled.
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