...
首页> 外文期刊>International Journal of Photoenergy >J-Aggregates of Amphiphilic Cyanine Dyes for Dye-Sensitized Solar Cells: A Combination between Computational Chemistry and Experimental Device Physics
【24h】

J-Aggregates of Amphiphilic Cyanine Dyes for Dye-Sensitized Solar Cells: A Combination between Computational Chemistry and Experimental Device Physics

机译:用于染料敏化太阳能电池的两性花青染料的J聚集体:计算化学与实验装置物理之间的组合

获取原文
获取原文并翻译 | 示例
           

摘要

We report on the design and structure principles of 5,5'-6,6'-tetrachloro-1,1'-dioctyl-3,3'-bis-(3-carboxypropyl)-benzimidacarbocyanine (Dye 1). Such metal-free amphiphilic cyanine dyes have many applications in dye-sensitized solar cells. AFM surface topographic investigation of amphiphilic molecules of Dye 1 adsorbed on TiO2 anode reveals the ability of spontaneous self-organization into highly ordered aggregates of fiber-like structure. These aggregates are known to exhibit outstanding optical properties of J-aggregates, namely, efficient exciton coupling and fast exciton energy migration, which are essential for building up artificial light harvesting to the photovoltaic device. A light-to-electricity conversion efficiency of DSSC based on the metal free amphiphilic Dye 1 is eta = 3.75 , which is about 50% of that based on metal-based N719 Ru-dye (Di-tetrabutylammoniumcis-bis(isothiocyanato)bis(2,2'-bipyridyl-4,4'-dicarboxylato)ruthenium(II)). DFT and TD-DFT studies show that large intramolecular charge transfer takes place from the HOMO to LUMO. HOMO is localized on a part of the molecule with almost no contribution from the carboxylic moiety. This clearly indicates that the anchoring carboxylic group plays a minor role.
机译:我们报告了5,5'-6,6'-四氯-1,1'-二辛基-3,3'-双-(3-羧丙基)-苯并咪唑基花菁(染料1)的设计和结构原理。这种无金属的两亲花青染料在染料敏化太阳能电池中具有许多应用。对TiO2阳极上吸附的Dye 1的两亲分子进行AFM表面形貌研究,揭示了自发自组织为纤维状结构的高度有序聚集体的能力。已知这些聚集体表现出J聚集体的优异光学性质,即有效的激子耦合和快速的激子能量迁移,这对于建立到光伏装置的人造光收集是必不可少的。基于不含金属的两性染料1的DSSC的光电转换效率为eta = 3.75,约为基于金属的N719 Ru-染料(Di-tetrabutylammonciscis-bis(isothiocyanato)bis( 2,2'-联吡啶基-4,4'-二羧基)钌(II))。 DFT和TD-DFT研究表明,大分子内电荷从HOMO转移到LUMO。 HOMO位于分子的一部分上,几乎没有羧基部分的贡献。这清楚地表明锚定羧基基团起次要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号