Deciphering Reaction Products in Formamidine-Based Perovskites with Methylammonium Chloride Additive

被引:33
作者
Chen, Liang [1 ]
Hu, Manman [1 ]
Lee, Seonghwan [2 ]
Kim, Jaehui [1 ]
Zhao, Zhi-Ying [3 ,4 ]
Han, Sun-Phil [5 ]
Lah, Myoung Soo [2 ]
Seok, Sang Il [1 ]
机构
[1] Ulsan Natl Inst Sci & Technol UNIST, Dept Energy & Chem Engn, Ulsan 44919, South Korea
[2] Ulsan Natl Inst Sci & Technol UNIST, Dept Chem, Ulsan 44919, South Korea
[3] Chinese Acad Sci, CAS Key Lab Design & Assembly Funct Nanostruct, Fujian Prov Key Lab Nanomat, Fuzhou 350002, Peoples R China
[4] Chinese Acad Sci, Fujian Inst Res Struct Matter, Fujian Prov Key Lab Nanomat, Fuzhou 350002, Peoples R China
[5] Ulsan Natl Inst Sci & Technol UNIST, UNIST Cent Res Facil UCRF, Ulsan 44919, South Korea
基金
新加坡国家研究基金会;
关键词
CARRIER DYNAMICS; LEAD IODIDE; CRYSTALS;
D O I
10.1021/jacs.3c12755
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The fabrication of formamidinium lead iodide (FAPbI(3)) perovskite solar cells (PSCs) involves the addition of methylammonium chloride (MACl) to promote low-temperature alpha-phase formation and grain growth. However, as the added MACl deprotonates and volatilizes into methylamine (MA(0)) and HCl for removal, MA(0) can chemically interact with formamidinium (FA(+)), forming methyl formamidinium (MFA(+)) as a byproduct. Despite its significance, the chemical interactions among FAPbI(3) perovskites, MACl additives, and their byproducts remain poorly understood. Our findings reveal that the FA(+) and MA(0) reaction primarily yields a mixture of cis/trans-N-methyl formamidinium iodide (MFAI) isomers, with cis-MFAI prevailing as the dominant species. Moreover, MFAI subsequently reacts with PbI2 to yield fully formed cis-MFAPbI(3) 2H-phase perovskite. We elucidated the effects of MFAI on the crystal growth, phase stability, and band gap of formamidine-based perovskites through the growth of single crystals. This research offers valuable insights into the role of these byproducts in influencing the efficiency and long-term stability of future PSCs.
引用
收藏
页码:27900 / 27910
页数:11
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