堆积
有机太阳能电池
三聚体
材料科学
分子间力
接受者
能量转换效率
异构化
光化学
光电子学
电致发光
光伏系统
激子
吸收(声学)
化学物理
二聚体
有机半导体
量子效率
电荷(物理)
聚合物太阳能电池
吸收光谱法
分子内力
有机发光二极管
混合太阳能电池
太阳能电池
密度泛函理论
重组
作者
Yuyang Bai,H. J. Yang,Jia Wang,Baofa Lan,Tianqi Chen,Yong Huo,Bin Kan
标识
DOI:10.1021/acs.chemmater.5c02690
摘要
The development of high-performance trimer acceptors (TMAs) for organic solar cells (OSCs) is often hampered by their blue-shifted absorption spectra. Consequently, to overcome this limitation and enhance device performance, we designed two propeller-shaped TMAs, TYSe-1 and TYSe-2, employing a multiselenophene strategy to achieve the desired redshift in absorption. In addition, side-chain isomerization was employed to tune the molecular packing and aggregation. The linear nonyl chains in TYSe-1 enabled tighter intermolecular stacking than the branched chains in TYSe-2, thus yielding an optimized blend morphology that enhanced exciton dissociation, charge transport, and charge extraction. Combined with its efficient absorption, TYSe-1-based OSCs achieved an outstanding short-circuit current density (JSC) value of 26.53 mA cm–2, ranking among the highest reported for TMA-based devices. Moreover, TYSe-1 exhibited higher electroluminescence quantum efficiency, leading to suppressed nonradiative recombination loss (ΔE3) and reduced overall energy loss. With an open-circuit voltage (VOC) value of approximately 0.857 V and an exceptional JSC value, TYSe-1-based OSCs attained a notable power conversion efficiency of 16.84%. These findings underscore the significant potential of the multiselenophene approach in designing red-shifted, high-performance TMA-based organic photovoltaics.
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