钝化
能量转换效率
钙钛矿(结构)
材料科学
盐(化学)
图层(电子)
光电子学
结晶度
降级(电信)
化学工程
纳米技术
化学
复合材料
有机化学
电子工程
工程类
作者
Hongru Ma,Minhuan Wang,Yudi Wang,Qingshun Dong,Jing Liu,Yanfeng Yin,Jie Zhang,Mingzhu Pei,Linghui Zhang,Wanxian Cai,Lei Shi,Wenming Tian,Shengye Jin,Jiming Bian,Yantao Shi
标识
DOI:10.1016/j.cej.2022.136291
摘要
For perovskite solar cells (PSCs), the presence of interfacial defects limits device’s efficiency and long-term stability. Reasonably passivating the interfacial defects and reducing the non-radiative recombination concerning perovskite layer are effective ways to achieve high-efficiency PSCs. Herein, we report an effective method by using an asymmetric diammonium salt of N, N-dimethyl-1,3-propanediamine dihydroiodide (DMAPAI2) buried in SnO2 layer to modify the interface between electron transport layer (ETL) and perovskite (PVK) layer. The burying of DMAPAI2 into SnO2 not only improves the electron mobility of SnO2 ETL, but also optimizes the energy level arrangement of ETL/PVK interface. In addition, the crystallinity of PVK is enhanced and the defects at the buried interface are passivated. Based on this strategy, the power conversion efficiency (PCE) of PSCs is significantly improved from 20.78% to 23.20%. Meanwhile, as compared to the control device, the DMAPAI2 modified PSCs exhibited better operational stability under 1-sun illumination at maximum power point, and retained over 85% of its initial PCE after 1200 h continuous irradiation. These results indicate that burying suitable ammonium salt in ETL is an effective interfacial modification strategy to boost the device’s PCE and stability.
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