Tang Fu-Ching, Wu Fu-Chiao, Yen Chia-Te, Chang Jay, Chou Wei-Yang, Gilbert Chang Shih-Hui, Cheng Horng-Long
Department of Physics, National Cheng Kung University, Tainan 701, Taiwan.
Nanoscale. 2015 Jan 7;7(1):104-12. doi: 10.1039/c4nr03176h.
In the optimization of organic solar cells (OSCs), a key problem lies in the maximization of charge carriers from the active layer to the electrodes. Hence, this study focused on the interfacial molecular configurations in efficient OSC charge extraction by theoretical investigations and experiments, including small molecule-based bilayer-heterojunction (sm-BLHJ) and polymer-based bulk-heterojunction (p-BHJ) OSCs. We first examined a well-defined sm-BLHJ model system of OSC composed of p-type pentacene, an n-type perylene derivative, and a nanogroove-structured poly(3,4-ethylenedioxythiophene) (NS-PEDOT) hole extraction layer. The OSC with NS-PEDOT shows a 230% increment in the short circuit current density compared with that of the conventional planar PEDOT layer. Our theoretical calculations indicated that small variations in the microscopic intermolecular interaction among these interfacial configurations could induce significant differences in charge extraction efficiency. Experimentally, different interfacial configurations were generated between the photo-active layer and the nanostructured charge extraction layer with periodic nanogroove structures. In addition to pentacene, poly(3-hexylthiophene), the most commonly used electron-donor material system in p-BHJ OSCs was also explored in terms of its possible use as a photo-active layer. Local conductive atomic force microscopy was used to measure the nanoscale charge extraction efficiency at different locations within the nanogroove, thus highlighting the importance of interfacial molecular configurations in efficient charge extraction. This study enriches understanding regarding the optimization of the photovoltaic properties of several types of OSCs by conducting appropriate interfacial engineering based on organic/polymer molecular orientations. The ultimate power conversion efficiency beyond at least 15% is highly expected when the best state-of-the-art p-BHJ OSCs are combined with present arguments.
在有机太阳能电池(OSC)的优化过程中,一个关键问题在于如何使从活性层到电极的电荷载流子最大化。因此,本研究通过理论研究和实验,聚焦于高效OSC电荷提取中的界面分子构型,研究对象包括基于小分子的双层异质结(sm - BLHJ)和基于聚合物的本体异质结(p - BHJ)OSC。我们首先研究了一个由p型并五苯、n型苝衍生物和纳米沟槽结构的聚(3,4 - 亚乙基二氧噻吩)(NS - PEDOT)空穴提取层组成的定义明确的OSC的sm - BLHJ模型系统。与传统平面PEDOT层相比,具有NS - PEDOT的OSC短路电流密度提高了230%。我们的理论计算表明,这些界面构型之间微观分子间相互作用的微小变化会导致电荷提取效率的显著差异。实验上,通过具有周期性纳米沟槽结构在光活性层和纳米结构电荷提取层之间产生了不同的界面构型。除了并五苯,还研究了p - BHJ OSCs中最常用的电子给体材料体系聚(3 - 己基噻吩)作为光活性层的可能性。使用局部导电原子力显微镜测量纳米沟槽内不同位置的纳米级电荷提取效率,从而突出了界面分子构型在高效电荷提取中的重要性。本研究通过基于有机/聚合物分子取向进行适当的界面工程,丰富了对几种类型OSC光伏性能优化的理解。当将最先进的p - BHJ OSCs与当前观点相结合时,有望实现至少15%的最终功率转换效率。