钙钛矿(结构)
材料科学
载流子
三卤化物
电子
千分尺
兴奋剂
卤化物
化学物理
光电效应
化学
吸收(声学)
光学
光电子学
扩散
纳米技术
物理
结晶学
无机化学
热力学
复合材料
量子力学
作者
Samuel D. Stranks,Giles E. Eperon,Giulia Grancini,Christopher Menelaou,Marcelo J. P. Alcocer,Tomas Leijtens,Laura M. Herz,Annamaria Petrozza,Henry J. Snaith
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2013-10-17
卷期号:342 (6156): 341-344
被引量:9288
标识
DOI:10.1126/science.1243982
摘要
Organic-inorganic perovskites have shown promise as high-performance absorbers in solar cells, first as a coating on a mesoporous metal oxide scaffold and more recently as a solid layer in planar heterojunction architectures. Here, we report transient absorption and photoluminescence-quenching measurements to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide (CH3NH3PbI(3-x)Cl(x)) and triiodide (CH3NH3PbI3) perovskite absorbers. We found that the diffusion lengths are greater than 1 micrometer in the mixed halide perovskite, which is an order of magnitude greater than the absorption depth. In contrast, the triiodide absorber has electron-hole diffusion lengths of ~100 nanometers. These results justify the high efficiency of planar heterojunction perovskite solar cells and identify a critical parameter to optimize for future perovskite absorber development.
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