离域电子
有机太阳能电池
电荷(物理)
异质结
电子
接受者
化学物理
激子
电子结构
光电子学
材料科学
辐射传输
工程物理
原子物理学
化学
物理
凝聚态物理
光学
量子力学
复合材料
聚合物
作者
Veaceslav Coropceanu,Xiankai Chen,Tonghui Wang,Zilong Zheng,Jean‐Luc Brédas
标识
DOI:10.1038/s41578-019-0137-9
摘要
In organic solar cells, the charge-transfer (CT) electronic states that form at the interface between the electron-donor (D) and electron-acceptor (A) materials have a crucial role in exciton-dissociation, charge-separation and charge-recombination processes. Since the introduction of active layers consisting of D–A bulk heterojunctions, CT states have been the focus of extensive experimental and theoretical studies. In this Review, we assess the current understanding of CT states and describe how factors such as the geometry of the D–A interface, electronic polarization and the extent of electron delocalization affect their nature and influence the radiative and non-radiative decay processes. We focus on the description and application of fundamental concepts, which provides the framework to discuss the path to organic solar cells with efficiencies comparable to those in inorganic photovoltaic technologies. The charge-transfer electronic states that form at the interfaces between electron-donor and electron-acceptor components have a key role in the electronic processes in organic solar cells. This Review describes the current understanding of how these charge-transfer states affect device performance.
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