光致发光
纳米晶
超晶格
材料科学
钙钛矿(结构)
卤化物
纳米技术
化学物理
光电子学
结晶学
化学
无机化学
作者
Dmitry Baranov,Antonio Fieramosca,Ruoxi Yang,Laura Polimeno,Giovanni Lerario,Stefano Toso,Carlo Giansante,Milena De Giorgi,Liang Z. Tan,D. Sanvitto,Liberato Manna
出处
期刊:ACS Nano
[American Chemical Society]
日期:2020-12-22
卷期号:15 (1): 650-664
被引量:76
标识
DOI:10.1021/acsnano.0c06595
摘要
Excitonic coupling, electronic coupling, and cooperative interactions in self-assembled lead halide perovskite nanocrystals were reported to give rise to a red-shifted collective emission peak with accelerated dynamics. Here we report that similar spectroscopic features could appear as a result of the nanocrystal reactivity within the self-assembled superlattices. This is demonstrated by studying CsPbBr3 nanocrystal superlattices over time with room-temperature and cryogenic micro-photoluminescence spectroscopy, X-ray diffraction, and electron microscopy. It is shown that a gradual contraction of the superlattices and subsequent coalescence of the nanocrystals occurs over several days of keeping such structures under vacuum. As a result, a narrow, low-energy emission peak is observed at 4 K with a concomitant shortening of the photoluminescence lifetime due to the energy transfer between nanocrystals. When exposed to air, self-assembled CsPbBr3 nanocrystals develop bulk-like CsPbBr3 particles on top of the superlattices. At 4 K, these particles produce a distribution of narrow, low-energy emission peaks with short lifetimes and excitation fluence-dependent, oscillatory decays. Overall, the aging of CsPbBr3 nanocrystal assemblies dramatically alters their emission properties and that should not be overlooked when studying collective optoelectronic phenomena nor confused with superfluorescence effects.
科研通智能强力驱动
Strongly Powered by AbleSci AI