材料科学
掺杂剂
钙钛矿(结构)
扩散
能量转换效率
磁滞
离子键合
载流子寿命
兴奋剂
载流子
钙钛矿太阳能电池
光电子学
吸附
化学工程
纳米技术
化学物理
离子
凝聚态物理
物理化学
硅
热力学
化学
物理
量子力学
工程类
作者
Lipeng Wang,Jianxing Xia,Yan Zheng,Peiquan Song,Chao Zhen,Xin Jiang,Guang Shao,Zeliang Qiu,Zhanhua Wei,Jianhang Qiu,Mohammad Khaja Nazeeruddin
标识
DOI:10.1002/adfm.202204725
摘要
Abstract The under‐coordinated defects within perovskite and its relevant interfaces always attract and trap the free carriers via the electrostatic force, significantly limiting the charge extraction efficiency and the intrinsic stability of perovskite solar cells (PSCs). Herein, self‐diffusion interfacial doping by using ionic potassium L‐aspartate (PL‐A) is first reported to restrain the carrier trap induced recombination via the reconstruction of energy level structure at SnO 2 /perovskite interface in conventional n‐i‐p structured PSCs. Experiments and theories are consistent with the PL‐A anions that can remain at the SnO 2 surface due to strong chemical adsorption. During the spin‐coating of the perovskite film, the cations gradually diffuse into perovskite and endow an n ‐doping effect, which provides higher force and a better energy level alignment for the carrier transport. As a result, they obtained 23.74% power conversion efficiency for the PL‐A modified small‐area devices, with dramatically improved open‐circuit voltage of 1.19 V. The corresponding large‐area devices (1.05 cm 2 ) achieved an efficiency of 22.23%. Furthermore, the modified devices exhibited negligible hysteresis and enhanced ambient air stability exceeding 1500 h.
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