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New insights into the design of conjugated polymers for intramolecular singlet fission

机译:分子内单线裂变共轭聚合物设计的新见解

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摘要

Singlet fission (SF), a multiple exciton generation process that generates two triplet excitons after the absorption of one photon, can potentially enable more efficient solar cell designs by harvesting energy normally lost as heat. While low-bandgap conjugated polymers are highly promising candidates for efficient SF-based solar cells, few polymer materials capable of SF have been reported because the SF process in polymer chains is poorly understood. Using transient spectroscopy, we demonstrate a new, highly efficient (triplet yield of 160–200%) isoindigo-based donor–acceptor polymer and show that the triplet pairs are directly emissive and exhibit a time-dependent energy evolution. Importantly, aggregation in poor solvents and in films significantly lowers the singlet energy, suppressing triplet formation because the energy conservation criterion is no longer met. These results suggest a new design rule for developing intramolecular SF capable low-bandgap conjugated polymers, whereby inter-chain interactions must be carefully engineered.
机译:单态裂变(SF)是一种多激子产生过程,在吸收一个光子后会产生两个三重态激子,可以通过收集通常以热量形式损失的能量来实现更高效的太阳能电池设计。虽然低带隙共轭聚合物是高效基于SF的太阳能电池的高度有前途的候选者,但由于对聚合物链中SF过程的了解不多,因此几乎没有报道能够使用SF的聚合物材料。使用瞬态光谱法,我们证明了一种新型的,高效的(三重态产率为160-200%)基于异靛蓝的供体-受体聚合物,并表明三重态对是直接发射的,并且表现出随时间变化的能量演化。重要的是,不良溶剂和薄膜中的聚集会显着降低单线态能量,从而抑制三线态的形成,因为不再符合节能标准。这些结果为开发分子内具有SF功能的低带隙共轭聚合物提供了新的设计规则,因此必须仔细设计链间相互作用。

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