Nastasi Francesco, Mineo Placido Giuseppe, Barichello Jessica, La Ganga Giuseppina, Di Marco Gaetano, Calogero Giuseppe, Cordaro Massimiliano
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, V. le F. Stagno D'Alcontres 31, University of Messina, 98166 Messina, Italy.
Department of Chemical Sciences, University of Catania, V. A. Doria 6, 95100 Catania, Italy.
Biomimetics (Basel). 2022 Aug 11;7(3):110. doi: 10.3390/biomimetics7030110.
In this study, two boronic acid BODIPYs are obtained through a microwave-assisted Knoevenagel reaction. The aim is to use them for the first time as dyes in a photosensitized solar cell (DSSC) to mimic chlorophyll photosynthesis, harvesting solar light and converting it into electricity. The microwave-assisted Knoevenagel reaction is a straightforward approach to extending the molecular conjugation of the dye and is applied for the first time to synthesize BODIPY's boronic acid derivatives. These derivatives have proved to be very useful for covalent deposition on titania. This work studies the photo-physical and electrochemical properties. Moreover, the photovoltaic performances of these two new dyes as sensitizers for DSSC are discussed. Experimental data show that both dyes exhibit photosensitizing activities in acetonitrile and water. In particular, in all the experiments, distyryl BODIPY was more efficient than styryl BODIPY. In this study, demonstrating the use of a natural component as a water-based electrolyte for boronic BODIPY sensitizers, we open new possibilities for the development of water-based solar cells.
在本研究中,通过微波辅助的克诺文纳格尔反应获得了两种硼酸氟硼二吡咯。目的是首次将它们用作光敏太阳能电池(DSSC)中的染料,以模拟叶绿素光合作用,收集太阳光并将其转化为电能。微波辅助的克诺文纳格尔反应是一种扩展染料分子共轭的直接方法,并且首次应用于合成硼酸氟硼二吡咯的衍生物。这些衍生物已被证明对于在二氧化钛上进行共价沉积非常有用。这项工作研究了光物理和电化学性质。此外,还讨论了这两种新型染料作为DSSC敏化剂的光伏性能。实验数据表明,两种染料在乙腈和水中均表现出光敏活性。特别是,在所有实验中,二苯乙烯基硼酸氟硼二吡咯比苯乙烯基硼酸氟硼二吡咯更有效。在本研究中,我们展示了使用天然成分作为硼酸氟硼二吡咯敏化剂的水基电解质,为水基太阳能电池的开发开辟了新的可能性。