Addition of Monovalent Silver Cations to CH3NH3PbBr3 Produces Crystallographically Oriented Perovskite Thin Films

被引:10
作者
Siegler, Timothy D. [1 ,2 ]
Zhang, Yangning [1 ,2 ]
Dolocan, Andrei [2 ]
Reimnitz, Lauren C. [1 ,2 ]
Torabi, Aida [4 ]
Abney, Michael K. [1 ,2 ]
Choi, Junho [3 ]
Cossio, Gabriel [5 ]
Houck, Daniel W. [1 ,2 ]
Yu, Edward T. [2 ,5 ]
Li, Xiaoqin [2 ,3 ]
Harvey, Taylor B. [4 ]
Milliron, Delia J. [1 ,2 ]
Korgel, Brian A. [1 ,2 ]
机构
[1] Univ Texas Austin, McKetta Dept Chem Engn, Complex Quantum Syst, Austin, TX 78712 USA
[2] Univ Texas Austin, Texas Mat Inst, Complex Quantum Syst, Austin, TX 78712 USA
[3] Univ Texas Austin, Dept Phys, Complex Quantum Syst, Austin, TX 78712 USA
[4] Texas A&M Univ Central Texas, Dept Sci & Math, Killeen, TX 76549 USA
[5] Univ Texas Austin, Dept Elect & Comp Engn, Microelect Res Ctr, Austin, TX 78758 USA
关键词
perovskite; methylammonium lead bromide (MAPBr); crystallographic texture; silver doping; surface segregation; perovskite photovoltaics; photoluminescence; POWER CONVERSION EFFICIENCY; SOLAR-CELLS; SINGLE-CRYSTAL; HALIDE PEROVSKITES; CRYSTALLIZATION; NANOCRYSTALS; DEGRADATION; PASSIVATION; PERFORMANCE; STABILITY;
D O I
10.1021/acsaem.9b01298
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
The incorporation of monovalent silver (Ag+) cations into methylammonium lead bromide (CH3NH3PbBr3) perovskite films leads to a strongly preferred (001) crystallographic orientation on a wide variety of substrates, ranging from glass to mesoporous TiO2. CH3NH3PbBr3 films deposited without Ag+ exhibit only a weakly preferred (011) orientation. Compositional maps and depth profiles from time-of-flight secondary ion mass spectrometry (TOF-SIMS) reveal Ag+ segregated to grain boundaries and interfaces. In photovoltaic devices (PVs), addition of Ag+ to MAPBr films resulted in poorer device performance, most likely because of the observed Ag+ segregation in the films.
引用
收藏
页码:6087 / 6096
页数:19
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