Interfacial Topochemical Fluoridation of MAPbI3 by Fluoropolymers

被引:3
|
作者
Lefler, Benjamin M. [1 ]
Houser, Theodore J. [2 ]
Chakrabarti, Arkita [2 ]
May, Steven J. [1 ]
Fafarman, Aaron T. [2 ]
机构
[1] Drexel Univ, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
[2] Drexel Univ, Dept Chem & Biol Engn, Philadelphia, PA 19104 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2023年 / 14卷 / 21期
基金
美国国家科学基金会;
关键词
PEROVSKITE SOLAR-CELLS; HIGH-EFFICIENCY; THIN-FILMS; FLUORINATION; DEGRADATION; LAMINATION; CHLORIDE; DEFECTS; OXIDES;
D O I
10.1021/acs.jpclett.3c00874
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Herein it is demonstrated that, under conditions relevantto perovskitesynthesis (>140 degrees C in air), fluoride can topochemically reactacross the interface between a halide perovskite and a fluoropolymerwhen in close contact, thereby creating a small quantity of stronglybonded lead fluoride species. The quantity increases with temperatureand processing duration. Photoinduced charge carrier lifetime providesa metric for the resulting changes in electronic structure of theperovskite. Under short-duration and/or moderate temperature processing,fluoride transfer to the perovskite yields increased carrier lifetimes,up to 3-fold longer than control samples, which is attributed to passivationof surface defects. Under more forcing conditions, the trend reverses:excessive fluoridation leads to shortened carrier lifetimes, whichis ascribed to substantial interfacial formation of PbF2. It is demonstrated that an interface with bulk crystalline PbF2 quenches perovskite photoluminescence, likely due to PbF2 serving as an electron acceptor for the conduction band ofMAPbI(3).
引用
收藏
页码:5040 / 5047
页数:8
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