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不对称铂(II)双(芳基乙炔基)配合物作为染料敏化太阳能电池的光敏剂。

Unsymmetric platinum(II) bis(aryleneethynylene) complexes as photosensitizers for dye-sensitized solar cells.

机构信息

Institute of Molecular Functional Materials, Department of Chemistry and Institute of Advanced Materials, Hong Kong Baptist University, Waterloo Road, Kowloon Tong, Hong Kong, P.R. China.

出版信息

Chem Asian J. 2012 Jun;7(6):1426-34. doi: 10.1002/asia.201200027. Epub 2012 Apr 11.

Abstract

Four new unsymmetric platinum(II) bis(aryleneethynylene) derivatives have been designed and synthesized, which showed good light-harvesting capabilities for application as photosensitizers in dye-sensitized solar cells (DSSCs). The absorption, electrochemical, time-dependent density functional theory (TD-DFT), impedance spectroscopic, and photovoltaic properties of these platinum(II)-based sensitizers have been fully characterized. The optical and TD-DFT studies show that the incorporation of a strongly electron-donating group significantly enhances the absorption abilities of the complexes. The maximum absorption wavelength of these four organometallic dyes can be tuned by various structural modifications of the triphenylamine and/or thiophene electron donor, improving the light absorption range up to 650 nm. The photovoltaic performance of these dyes as photosensitizers in mesoporous TiO(2) solar cells was investigated, and a power conversion efficiency as high as 1.57% was achieved, with an open-circuit voltage of 0.59 V, short-circuit current density of 3.63 mA cm(-2), and fill factor of 0.73 under simulated AM 1.5G solar illumination.

摘要

已经设计并合成了四个新的不对称铂(II)双(芳基乙炔基)衍生物,它们具有良好的光捕获能力,可作为染料敏化太阳能电池(DSSC)中的光敏剂。这些基于铂(II)的敏化剂的吸收、电化学、时间依赖密度泛函理论(TD-DFT)、阻抗谱和光伏性能已得到充分表征。光学和 TD-DFT 研究表明,引入强供电子基团可显著增强配合物的吸收能力。通过对三苯胺和/或噻吩给体进行各种结构修饰,可以调节这四个金属有机染料的最大吸收波长,将光吸收范围提高到 650nm 左右。研究了这些染料作为介孔 TiO2 太阳能电池中的光敏剂的光伏性能,在模拟 AM 1.5G 太阳光照下,实现了高达 1.57%的功率转换效率,开路电压为 0.59V,短路电流密度为 3.63mA/cm-2,填充因子为 0.73。

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