Luminescent Intermediates and Humidity-Dependent Room-Temperature Conversion of the MAPbI3 Perovskite Precursor

被引:23
|
作者
Li, Jun [1 ,2 ]
Dobrovolsky, Alexander [1 ,2 ]
Merdasa, Aboma [3 ]
Unger, Eva L. [1 ,2 ,3 ]
Scheblykin, Ivan G. [1 ,2 ]
机构
[1] Lund Univ, Chem Phys, POB 124, S-22100 Lund, Sweden
[2] Lund Univ, NanoLund, POB 124, S-22100 Lund, Sweden
[3] Helmholtz Zentrum Berlin Mat & Energie GmbH, D-12489 Berlin, Germany
来源
ACS OMEGA | 2018年 / 3卷 / 10期
基金
瑞典研究理事会;
关键词
SOLAR-CELLS; THIN-FILMS; RELATIVE-HUMIDITY; 2-STEP DEPOSITION; LEAD(II) IODIDE; CH3NH3PBI3; DEGRADATION; PERFORMANCE; GROWTH; CH(3)NH(3)PBL(3);
D O I
10.1021/acsomega.8b01799
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Preparation of metal-halide perovskites under room temperature attracts attention because of energy saving by removing thermal annealing. Room-temperature transformation of spin-cast wet films consisting of methylammonium (MA) iodide, PbI2, and dimethylformamide toward solid MAPbI(3) perovskite proceeds via several intermediate crystalline states and is strongly dependent on ambient humidity. Light transmission and photoluminescence (PL) microscopy and spectroscopy were used to monitor the growth of crystals and transformation of their properties in time under nitrogen atmosphere at room temperature. Under low humidity, a highly luminescent intermediate phase with low absorption in the visible range appears, with the PL spectra composed of several bands in the range from 600 to 760 nm. We assign these bands to low-dimensional (nanocrystals and two-dimensional inclusions) MAPbI(3) intermediates, where the exciton confinement shifts the spectrum to higher energies in comparison with the bulk MAPbI(3). The intermediate levels of ambient humidity (10-50%) appear to catalyze the conversion of the intermediate phase to MAPbI(3). At a high ambient humidity (>80%), the initially formed MAPbI3 is quickly transformed to the transparent hydrate phase of MAPbI(3). The role of ambient water catalyzing the material transformation by competing for Pb coordination with the solvent molecules is discussed.
引用
收藏
页码:14494 / 14502
页数:9
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