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Effects of Bulky Substituents of Push-Pull Porphyrins on Photovoltaic Properties of Dye-Sensitized Solar Cells

机译:推挽卟啉的大体积取代基对染料敏化太阳能电池光伏性能的影响

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摘要

To evaluate the effects of substituent bulkiness around a porphyrin core on the photovoltaic properties of porphyrin-sensitized solar cells, long alkoxy groups were introduced at the meso-phenyl group (ZnPBAT-o-C8) and the anchoring group (ZnPBAT-o-C8Cn, n = 4, 8) of an asymmetrically substituted push-pull porphyrin with double electron-donating diarylamino groups and a single electron-withdrawing carboxyphenylethynyl anchoring group. The spectroscopic and electrochemical properties of ZnPBAT-o-C8 and ZnPBAT-o-C8Cn were found to be superior to those of a push pull porphyrin reference (YD2-o-C8), demonstrating their excellent light-harvesting and redox properties for dye-sensitized solar cells. A power conversion efficiency (eta) of the ZnPBAT-o-C8-sensitized solar cell (eta = 9.1%) is higher than that of the YD2-o-C8-sensitized solar cell (eta = 8.6%) using iodine-based electrolyte due to the enhanced light-harvesting ability of ZnPBAT-o-C8. In contrast, the solar cells based on ZnPBAT-o-C8Cn, possessing the additional alkoxy chains in the anchoring group, revealed the lower eta values of 7.3% (n = 4) and 7.0% (n = 8). Although ZnPBAT-o-C8Cn exhibited higher resistance at the TiO2 dye electrolyte interface by virtue of the extra alkoxy chains, the reduced amount of the porphyrins on TiO2 by excessive addition of coadsorbent chenodeoxycholic acid (CDCA) for mitigating the aggregation on TiO2 resulted in the low eta values: Meanwhile, the ZnPBAT-o-C8-sensitized solar cell showed the lower eta value of 8.1% than the YD2-o-C8-sensitized solar cell (eta = 9.8%) using cobalt-based electrolyte. The smaller eta value of the ZnPBAT-o-C8-sensitized solar cell may be attributed to the insufficient blocking effect of the bulky substituents of ZnPBAT-o-C8 under the cobalt-based electrolyte conditions. Overall, the alkoxy chain length and substitution position around the porphyrin core are important factors to affect the cell performance.
机译:为了评估卟啉核心周围的取代基庞大对卟啉敏化太阳能电池的光伏性能的影响,在中苯基(ZnPBAT-o-C8)和锚定基团(ZnPBAT-o-C8Cn)处引入了长烷氧基,n = 4,8)的不对称取代推挽卟啉具有两个供电子的二芳基氨基和一个吸电子的羧基苯基乙炔基锚定基团。发现ZnPBAT-o-C8和ZnPBAT-o-C8Cn的光谱和电化学性能优于推拉式卟啉参比(YD2-o-C8),证明了它们对染料的优异的光吸收和氧化还原性能。敏化太阳能电池。使用基于碘的电解质的ZnPBAT-o-C8敏化的太阳能电池(eta = 9.1%)的功率转换效率(eta)高于YD2-o-C8敏化的太阳能电池(eta = 8.6%)由于增强了ZnPBAT-o-C8的光捕获能力。相反,基于ZnPBAT-o-C8Cn的太阳能电池在锚定基团中具有附加的烷氧基链,其eta值较低,分别为7.3%(n = 4)和7.0%(n = 8)。尽管ZnPBAT-o-C8Cn通过额外的烷氧基链在TiO2染料电解质界面处表现出更高的电阻,但通过过量添加共吸附性去氧胆酸(CDCA)来减轻TiO2上的聚集,减少了TiO2上的卟啉量。低eta值:同时,ZnPBAT-o-C8敏化的太阳能电池比使用钴基电解质的YD2-o-C8敏化的太阳能电池(eta = 9.8%)显示更低的eta值8.1%。 ZnPBAT-o-C8敏化的太阳能电池的eta值较小,可能是由于在钴基电解质条件下ZnPBAT-o-C8的大取代基的阻断作用不足所致。总体而言,卟啉核心周围的烷氧基链长度和取代位置是影响细胞性能的重要因素。

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