Jiang Miao, Wang Rui, Deng Zijian, Xu Gongchen, Shangguan Qing, Sun Licheng, Zhang Li, Yang Xichuan
Institute of Artificial Photosynthesis, State Key Laboratory of Fine Chemicals, DUT-KTH Joint Education and Research Centre on Molecular Devices, Dalian University of Technology (DUT), 2 Linggong Road, Dalian 116024, China.
Center of Artificial Photosynthesis for Solar Fuels, School of Science, Westlake University, Hangzhou 310024, China.
ACS Appl Mater Interfaces. 2024 Sep 25;16(38):51265-51273. doi: 10.1021/acsami.4c12311. Epub 2024 Sep 11.
Single dyes typically exhibit limited light absorption in dye-sensitized solar cells (DSSCs). Thus, cosensitization using two or more dyes to enhance light-harvesting efficiency has been explored; however, the aggregation of dyes can adversely affect electron injection capabilities. This study focused on the design and synthesis of three dyes with a common carbazole donor for DSSCs: , , and . broadens the absorption spectrum by replacing the benzoic acid electron acceptor of with acetylenic benzoic acid. A cosensitized DSSC device based on CO-1 [: = 1:1 (50 μM:50 μM)] achieved a short-circuit current density of 19.4 mA/cm and a power conversion efficiency of 10.9%. For the first time, the molecular interactions between the dyes in the photoanode were demonstrated using cyclic voltammetry, which revealed the presence of intermolecular forces. Adsorption kinetics further indicated that these forces promoted the self-assembly of dyes during adsorption, which resulted in a cosensitization adsorption amount greater than the sum of the individual dye adsorptions. This study provides novel insights into the selection of cosensitizing dyes for DSSCs.
在染料敏化太阳能电池(DSSC)中,单一染料通常表现出有限的光吸收。因此,人们探索了使用两种或更多种染料进行共敏化以提高光捕获效率;然而,染料的聚集会对电子注入能力产生不利影响。本研究聚焦于设计和合成三种用于DSSC的具有共同咔唑供体的染料: 、 和 。 通过用炔基苯甲酸取代 的苯甲酸电子受体来拓宽吸收光谱。基于CO - 1 [ := 1:1(50 μM:50 μM)]的共敏化DSSC器件实现了19.4 mA/cm的短路电流密度和10.9%的功率转换效率。首次使用循环伏安法证明了光阳极中染料之间的分子相互作用,这揭示了分子间力的存在。吸附动力学进一步表明,这些力在吸附过程中促进了染料的自组装,导致共敏化吸附量大于各单个染料吸附量之和。本研究为DSSC共敏化染料的选择提供了新的见解。