Chen Chia-Yuan, Lin Ting-Yi, Chiu Chi-Feng, Lee Mandy M, Li Wei-Long, Chen Min-Yu, Hung Tzu-Hao, Zhang Zhao-Jie, Tsai Hui-Hsu Gavin, Sun Shih-Sheng, Wu Chun-Guey
Research Center of New Generation Light Driven Photovoltaic Modules and, National Central University, Taoyuan 32001, Taiwan, R.O.C.
Department of Chemistry, National Central University, Taoyuan 32001, Taiwan, R.O.C.
ACS Appl Mater Interfaces. 2024 Mar 13;16(10):12647-12660. doi: 10.1021/acsami.3c19298. Epub 2024 Mar 4.
Three new heteroleptic Ru complexes, , , and , were prepared as sensitizers for coadsorbent-free, panchromatic, and efficient dye-sensitized solar cells. They are simultaneously functionalized with highly conjugated anchoring and ancillary ligands to explore the electronic and steric effects on their photovoltaic characteristics. The coadsorbent-free device based on achieved the best power conversion efficiency (PCE) of 8.63% and a panchromatic response extending to 850 nm. The two stereoisomers, and coordinated with an unsymmetrical anchoring ligand, display similar absorption properties and the same driving forces for electron injection as well as dye regeneration. Nevertheless, the devices show not only the remarkably distinct PCE (6.64% vs 8.38%) but also discernible stability. The molecular simulation for the two stereoisomers adsorbed on TiO clarifies the distinguishable distances (16.9 Å vs 19.0 Å) between the sulfur atoms in the NCS ligands and the surface of the TiO, dominating the charge recombination dynamics and iodine binding and therefore the PCE and stability of the devices. This study on the steric effects caused by the highly conjugated and unsymmetrical anchoring ligand on the adsorption geometry and photovoltaic performance of the dyes paves a new way for advancing the molecular design of polypyridyl metal complex sensitizers.
制备了三种新型杂配钌配合物,即[具体配合物1]、[具体配合物2]和[具体配合物3],作为无共吸附剂、全色且高效的染料敏化太阳能电池的敏化剂。它们同时用高度共轭的锚定配体和辅助配体进行功能化,以探究其对光伏特性的电子和空间效应。基于[具体配合物1]的无共吸附剂器件实现了8.63%的最佳功率转换效率(PCE)以及延伸至850 nm的全色响应。与不对称锚定配体配位的两种立体异构体[具体立体异构体1]和[具体立体异构体2],表现出相似的吸收特性以及相同的电子注入驱动力和染料再生能力。然而,这些器件不仅显示出显著不同的PCE(6.64%对8.38%),而且稳定性也可辨别。对吸附在TiO₂上的两种立体异构体进行的分子模拟表明,NCS配体中硫原子与TiO₂表面之间的距离存在明显差异(16.9 Å对19.0 Å),这主导了电荷复合动力学和碘结合,进而决定了器件的PCE和稳定性。这项关于高度共轭且不对称的锚定配体对染料吸附几何结构和光伏性能所产生的空间效应的研究,为推进多吡啶金属配合物敏化剂的分子设计开辟了一条新途径。