Guo Huijie, Wang Xinyue, Zhang Meixia, Pullerits Tõnu, Song Peng
College of Physics, Liaoning University, Shenyang 110036, China.
Department of Chemical Physics, Lund University, Box 124, Lund 22100, Sweden.
Spectrochim Acta A Mol Biomol Spectrosc. 2025 Jan 15;325:125058. doi: 10.1016/j.saa.2024.125058. Epub 2024 Aug 28.
In organic solar cells (OSCs), comprehending the charge transfer mechanism at D/A interfaces is crucial for photoinduced charge generation and enhancing power conversion efficiency (PCE). The charge transfer mechanism and photovoltaic performance of the parallel stacking interface configuration of the PTQ10 polymer donor and T2EH non-fullerene acceptor (NFA) are systematically studied at the microscopic scale. The analysis of the electron-hole distribution of the PTQ10/T2EH excited states revealed the presence of multiple charge excitation modes and charge transfer pathways. Using Marcus theory, we examine the charge separation rate (K) of PTQ10/T2EH under external electric field (F) modulation, and it is clarified that reorganization energy (λ) is the main factor that affects the K. Our results show that F has a positive impact on the photovoltaic properties of PTQ10/T2EH thin films, as evidenced by the modulation of the open circuit voltage (V), voltage loss (V) and fill factor (FF). Overall, this study provides valuable theoretical insights for F to accelerate the charge separation process and enhance photovoltaic efficiency.
在有机太阳能电池(OSC)中,理解给体/受体(D/A)界面处的电荷转移机制对于光生电荷的产生和提高功率转换效率(PCE)至关重要。在微观尺度上系统地研究了PTQ10聚合物给体和T2EH非富勒烯受体(NFA)的平行堆叠界面结构的电荷转移机制和光伏性能。对PTQ10/T2EH激发态的电子-空穴分布分析揭示了多种电荷激发模式和电荷转移途径的存在。利用Marcus理论,我们研究了外部电场(F)调制下PTQ10/T2EH的电荷分离速率(K),并阐明了重组能(λ)是影响K的主要因素。我们的结果表明,F对PTQ10/T2EH薄膜的光伏性能有积极影响,开路电压(V)、电压损失(V)和填充因子(FF)的调制证明了这一点。总体而言,本研究为F加速电荷分离过程和提高光伏效率提供了有价值的理论见解。