Affiliation:
1. The Institute of Technological Sciences Wuhan University Wuhan 430072 P. R. China
2. School of Physics and Technology Wuhan University Wuhan 430072 P. R. China
3. Key Laboratory of Optoelectronic Chemical Materials and Devices (Ministry of Education) Flexible Display Materials and Technology Co-Innovation Centre of Hubei Province School of Optoelectronic Materials & Technology Jianghan University Wuhan 430056 China
4. College of Materials Science and Engineering & Institute of New Energy and Low-Carbon Technology Sichuan University Chengdu 610065 China
Abstract
AbstractLow band gap tin‐lead perovskite solar cells (Sn−Pb PSCs) are expected to achieve higher efficiencies than Pb‐PSCs and regarded as key components of tandem PSCs. However, the realization of high efficiency is challenged by the instability of Sn2+and the imperfections at the charge transfer interfaces. Here, we demonstrate an efficient ideal band gap formamidinium (FA)‐based Sn−Pb (FAPb0.5Sn0.5I3) PSC, by manipulating the buried NiOx/perovskite interface with 4‐hydroxyphenethyl ammonium halide (OH‐PEAX, X=Cl−, Br−, or I−) interlayer, which exhibits fascinating functions of reducing the surface defects of the NiOxhole transport layer (HTL), enhancing the perovskite film quality, and improving both the energy level matching and physical contact at the interface. The effects of different halide anions have been elaborated and a 20.53 % efficiency is obtained with OH‐PEABr, which is the highest one for FA‐based Sn−Pb PSCs using NiOxHTLs. Moreover, the device stability is also boosted.
Funder
National Natural Science Foundation of China
Subject
General Chemistry,Catalysis
Cited by
18 articles.
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