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A nanoscale study of charge extraction in organic solar cells: the impact of interfacial molecular configurations

机译:有机太阳能电池中电荷提取的纳米级研究:界面分子构型的影响

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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.
机译:在优化有机太阳能电池(OSC)时,一个关键问题在于电荷载体从活性层到电极的最大化。因此,这项研究的重点是通过理论研究和实验,包括基于小分子的双层 - 异位结合结(SM-BLHJ)和聚合物基基体积 - 异位结构(P-BHJ)OSCS,介绍了有效的OSC电荷提取中的界面分子构型。我们首先检查了由P型五苯甲苯烯,N型perylene衍生物和纳米根结构的聚(3,4-乙基二苯乙烯)(NS-PEDOT)孔提取层组成的OSC的定义明确的SM-BLHJ模型系统。与常规平面PEDOT层相比,具有NS-PEDOT的OSC在短路电流密度中显示出230%的增量。我们的理论计算表明,这些界面构型之间微分子间相互作用的微小变化可能会引起电荷提取效率的显着差异。在实验上,使用周期性纳米植物结构在光活动层和纳米结构电荷提取层之间生成不同的界面构型。除五苯五烯,聚(3-己基噻吩)外,还探索了P-BHJ OSC中最常用的电子借方材料系统,它的可能用作光活性层。局部导电原子力显微镜用于测量纳米根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有效电荷提取中的重要性。这项研究丰富了人们通过基于有机/聚合物分子方向进行适当的界面工程来优化几种类型OSC的光伏特性的理解。当最佳最先进的P-BHJ OSC与当前的论点相结合时,高度预期的最终功率转换效率至少超过15%。

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