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用于太阳能电池和非线性光学材料的新型芳基偶氮噻唑基噻吩染料的合成

Synthesis of Novel Arylazothiazolyl-thiophene Dyes for Solar Cell and Nonlinear Optical Materials.

作者信息

Khalifa Mohamed E, Al-Amoudi Muhammed S, Gobouri Adil A, Merazga Amar, Fadda Ahmed A

出版信息

Acta Chim Slov. 2016;63(1):121-8. doi: 10.17344/acsi.2015.2018.

Abstract

Synthesis and investigation of new donor-acceptor conjugated N-(5-arylazothiazol-2-yl)-2-aminothiophene derivatives with the aim to elucidate the contribution of their interaction with solvent molecules upon intramolecular charge transfer for their potential solar cells application. The UV-visible and emission spectra measurements indicated that the properties of the synthesized dyes had a significant effect on the visible absorption and emission maxima. The effect of the donor and acceptor groups were studied for the nonlinearity based on their HOMO-LUMO band gap energy. The dye-sensitized solar cells (DSSCs) were assembled by using the newly synthesized aryl thiazolyl-thiophene dyes as sensitizers. The promising results of J(SC) (2.46 × 10(-2) and 4.07 × 10(-2) mA/cm(2)), the V(OC) (0.429 V and 0.426 V) and the FF (0.66 %) values obtained comparing with other organic and natural sensitizer were due to the better interaction between the carboxyl and carbonyl groups of aryl azo molecule attached to the thiazolyl nucleus and the surface of TiO(2) porous film.

摘要

新型供体-受体共轭N-(5-芳基偶氮噻唑-2-基)-2-氨基噻吩衍生物的合成与研究,旨在阐明其与溶剂分子相互作用对分子内电荷转移的贡献,以用于潜在的太阳能电池应用。紫外可见光谱和发射光谱测量表明,合成染料的性质对可见光吸收和发射最大值有显著影响。基于其最高占据分子轨道-最低未占据分子轨道带隙能量,研究了供体和受体基团对非线性的影响。通过使用新合成的芳基噻唑基噻吩染料作为敏化剂组装了染料敏化太阳能电池(DSSC)。与其他有机和天然敏化剂相比,获得的J(SC)(2.46×10(-2)和4.07×10(-2) mA/cm(2))、V(OC)(0.429 V和0.426 V)以及填充因子(FF)(0.66%)的 promising 结果,归因于连接到噻唑核上的芳基偶氮分子的羧基和羰基与TiO(2)多孔膜表面之间更好的相互作用。

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