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首页> 外文期刊>RSC Advances >Synthesis, optical, electrochemical and photovoltaic properties of a D-pi-A fluorescent dye with triazine ring as electron-withdrawing anchoring group for dye-sensitized solar cells
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Synthesis, optical, electrochemical and photovoltaic properties of a D-pi-A fluorescent dye with triazine ring as electron-withdrawing anchoring group for dye-sensitized solar cells

机译:以三嗪环为吸电子锚定基团的D-pi-A荧光染料的合成,光学,电化学和光电性质

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摘要

The D-pi-A fluorescent dye OUJ-1 with 1,3,5-triazine ring as electron-withdrawing anchoring group and (diphenylamino) carbazole containing a thiophene ring as D-pi moiety have been newly developed and their optical and electrochemical properties, adsorption states on TiO2 nanoparticles, and photovoltaic performance in dye-sensitized solar cell (DSSC) were investigated. The absorption maximum (lambda(abs)(max)) for the intramolecular charge-transfer (ICT) absorption band of the D-pi-A dye OUJ-1 occurs at a longer wavelength than those of D-pi-A dye NI-6 with a pyridyl group and D-pi-A dye OUK-1 with a pyrzayl group. Moreover, the dye OUJ-1 exhibits significant fluorescence solvatochromic properties, that is, a bathochromic shift of the fluorescence band and a decrease in the fluorescence quantum yield (Phi) due to a change from the (ICT)-I-1 excited state to the twisted intramolecular charge transfer (TICT) excited state with increasing solvent polarity were observed. The photovoltaic performance of a DSSC based on OUJ-1 is lower than those of NI-6 and OUK-1 due to the low dye loading of OUJ-1 on TiO2 electrode. It was found that the dye OUJ-1 is adsorbed onto the TiO2 surface through the formation of trizainium ions at the Bronsted acid sites (surface-bound hydroxyl groups, Ti-OH) on the TiO2 surface, although the dye NI-6 was predominantly adsorbed on the TiO2 through coordinate bonding between the pyridyl group of the dye and the Lewis acid sites (exposed Tin+ cations) on the TiO2 surface, and the dye OUK-1 was adsorbed on the TiO2 surface through both the formations of hydrogen bonding of pyrazyl groups and pyrazinium ions at Bronsted acid sites on the TiO2 surface. This work revealed that the binding mode of D-pi-A dye sensitizers with azine rings on the TiO2 surface can be changed by control of the basicity and electron density of the azine rings.
机译:以1,3,5-三嗪环为吸电子锚定基团的D-pi-A荧光染料OUJ-1和以噻吩环为D-pi部分的(二苯氨基)咔唑为研究对象,对其光学和电化学性能进行了研究。 ,TiO2纳米粒子上的吸附状态和染料敏化太阳能电池(DSSC)的光伏性能进行了研究。 D-pi-A染料OUJ-1的分子内电荷转移(ICT)吸收带的最大吸收值(lambda(abs)(max))比D-pi-A染料NI-的更长的波长出现具有吡啶基的6和具有吡唑基的D-pi-A染料OUK-1。此外,染料OUJ-1表现出显着的荧光溶剂变色特性,即由于从(ICT)-I-1激发态变为荧光态而导致荧光带的红移和荧光量子产率(Phi)的降低。观察到随着溶剂极性的增加分子扭曲的分子内电荷转移(TICT)激发态。基于OUJ-1的DSSC的光伏性能低于NI-6和OUK-1的光伏性能,这是因为OUJ-1在TiO2电极上的染料负载量低。发现染料OUJ-1通过在TiO2表面上的布朗斯台德酸位点(表面结合的羟基,Ti-OH)上形成三嗪鎓离子而吸附在TiO2表面上,尽管染料NI-6主要是通过染料的吡啶基与TiO2表面上的路易斯酸位点(暴露的锡+阳离子)之间的配位键吸附在TiO2上,染料OUK-1通过吡唑基的氢键形成两种方式吸附在TiO2表面上在TiO2表面的布朗斯台德酸位上的基团和吡嗪鎓离子。这项工作表明D-pi-A染料敏化剂与TiO2表面上的嗪环的结合方式可以通过控制嗪环的碱度和电子密度来改变。

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