开路电压
材料科学
钙钛矿(结构)
光电子学
图层(电子)
带隙
接口(物质)
太阳能电池
电压
钙钛矿太阳能电池
偶极子
工程物理
纳米技术
电气工程
复合材料
化学
物理
结晶学
毛细管数
毛细管作用
工程类
有机化学
作者
Jihyeon Heo,Juan Anthony Prayogo,Seok Woo Lee,Hansol Park,Senthilkumar Muthu,JeeHee Hong,Haeun Kim,Young‐Hoon Kim,Dong Ryeol Whang,Dong Wook Chang,Hui Joon Park
出处
期刊:Small
[Wiley]
日期:2024-08-29
卷期号:20 (50)
被引量:2
标识
DOI:10.1002/smll.202404784
摘要
Abstract Wide‐bandgap perovskite solar cells (PSCs) with high open‐circuit voltage ( V oc ) represent a compelling and emerging technological advancement in high‐performing perovskite‐based tandem solar cells. Interfacial engineering is an effective strategy to enhance V oc in PSCs by tailoring the energy level alignments between the constituent layers. Herein, n‐type quinoxaline‐phosphine oxide‐based small molecules with strong dipole moments is designed and introduce them as effective cathode interfacial layers. Their strong dipole effect leads to appropriate energy level alignment by tuning the work function of the Ag electrode to form an ohmic contact and enhance the built‐in potential within the device, thereby improving charge‐carrier transport and mitigating charge recombination. The organic interfacial layer‐modified wide‐bandgap PSCs exhibit a high V oc of 1.31 V (deficit of <0.44 V) and a power conversion efficiency (PCE) of 20.3%, significantly improved from the device without an interface dipole layer ( V oc of 1.26 V and PCE of 16.7%). Furthermore, the hydrophobic characteristics of the small molecules contribute to improved device stability, retaining 95% of the initial PCE after 500 h in ambient air.
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