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Synthesis of a new photochromic ZrO{sub}2 precursor for preparation of functional thin films

机译:用于制备功能性薄膜的新光致变色ZrO {Sub} 2的合成

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A new photochromic ZrO{sub}2 precursor solution was prepared using zirconium tetra-n-butoxide, 4-(phenylazo)benzoic acid and ethyleneglycol monomethylether. The ZrO{sub}2 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 ZrO{sub}2 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 ZrO{sub}2 precursor was derived by density functional theory (DFT) calculation.
机译:使用锆四正丁醇氧化锆,4-(苯基氮杂)苯甲酸和乙二醇单甲基醚制备新的光致变色ZrO {亚} 2前体溶液。在室温下用紫外线(UV)照射ZrO {亚} 2前体溶液。之后,用在室温下用可见光(VI)照射UV辐照的前体溶液。在紫外线照射和辐射后测量UV-Vis光谱。 UV-Vis光谱的变化表明,包括4-(苯氮杂)苯甲酸的新ZrO {亚} 2前体显示光致变量。该现象与前体中4-(苯基氮杂)苯甲酸的可逆光学硅白化同步。另外,源自紫外线照射前的Zr-o CT转变的峰值的差异随着4-(苯基苯基)苯甲酸的浓度而增加。此外,通过密度泛函理论(DFT)计算来源的新Zro {Sub} 2前体的优化结构。

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