Time-resolved photoluminescence studies of perovskite chalcogenides

被引:0
|
作者
Ye, Kevin [1 ]
Zhao, Boyang [2 ]
Diroll, Benjamin T. [3 ]
Ravichandran, Jayakanth [2 ,4 ]
Jaramillo, R. [1 ]
机构
[1] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[2] Univ Southern Calif, Mork Family Dept Chem Engn & Mat Sci, Los Angeles, CA 90089 USA
[3] Argonne Natl Lab, Ctr Nanoscale Mat, Lemont, IL 60439 USA
[4] Univ Southern Calif, Ming Hsieh Dept Elect & Comp Engn, Los Angeles, CA 90089 USA
基金
美国国家科学基金会;
关键词
BAZRS3;
D O I
10.1039/d2fd00047d
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
Chalcogenides in the perovskite and related crystal structures ("chalcogenide perovskites" for brevity) may be useful for future optoelectronic and energy-conversion technologies inasmuch as they have good excited-state, ambipolar transport properties. In recent years, several studies have suggested that semiconductors in the Ba-Zr-S system have slow non-radiative recombination rates. Here, we present a time-resolved photoluminescence (TRPL) study of excited-state carrier mobility and recombination rates in the perovskite-structured material BaZrS3, and the related Ruddlesden-Popper phase Ba3Zr2S7. We measure state-of-the-art single crystal samples, to identify properties free from the influence of secondary phases and random grain boundaries. We model and fit the data using a semiconductor physics simulation, to enable more direct determination of key material parameters than is possible with empirical data modeling. We find that both materials have Shockley-Read-Hall recombination lifetimes on the order of 50 ns and excited-state diffusion lengths on the order of 5 mu m at room temperature, which bodes well for ambipolar device performance in optoelectronic technologies including thin-film solar cells.
引用
收藏
页码:146 / 159
页数:14
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