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Effects of anchoring groups in multi-anchoring organic dyes with thiophene bridge for dye-sensitized solar cells

机译:噻吩桥多锚定有机染料中锚固基团对染料敏化太阳能电池的影响

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摘要

Organic photo-sensitizers were designed and synthesized based on a phenothiazine framework containing single- and double-electron acceptors that were bridged with thiophene for the dye sensitized solar cells (DSSCs). The optimized geometries were determined with density functional theory (DFT) calculations to estimate the photovoltaic properties of the dyes in the design stage. The organic dye with the double electron acceptors exhibited a better light absorption at long wavelength and an effective electron extraction pathway from the electron donor to the TiO_2 surface, leading to an improved short-circuit current (11.6mA cm~(-2)), compared with that of the dye with the single electron acceptor (10.2 mAcm~(-2)) and the conventional N3 Ru-dye (10.4mAcm~(-2)). Contrarily, the open-circuit voltage of the organic dye with the double electron acceptors decreased because the additional protonated carboxylic groups caused a positive shift in the Fermi level of TiO_2.
机译:基于吩噻嗪骨架设计并合成了有机光敏剂,该骨架包含单电子和双电子受体,并与噻吩桥接,用于染料敏化太阳能电池(DSSC)。使用密度泛函理论(DFT)计算来确定优化的几何形状,以估计染料在设计阶段的光伏性质。具有双电子受体的有机染料在长波长下表现出更好的吸收光,并且从电子供体到TiO_2表面具有有效的电子提取路径,从而改善了短路电流(11.6mA cm〜(-2)),与具有单电子受体(10.2 mAcm〜(-2))和常规N3 Ru染料(10.4mAcm〜(-2))的染料相比。相反,具有双电子受体的有机染料的开路电压降低,因为附加的质子化的羧基导致TiO_2的费米能级发生正向偏移。

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