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全无机钙钛矿纳米晶的光致可逆相转变。

Photoinduced, reversible phase transitions in all-inorganic perovskite nanocrystals.

机构信息

Department of Chemistry, Northwestern University, Evanston, IL, 60208, USA.

Center for Nanoscale Materials, Argonne National Laboratory, Lemont, IL, 60439, USA.

出版信息

Nat Commun. 2019 Jan 30;10(1):504. doi: 10.1038/s41467-019-08362-3.

Abstract

Significant interest exists in lead trihalides that present the perovskite structure owing to their demonstrated potential in photovoltaic, lasing, and display applications. These materials are also notable for their unusual phase behavior often displaying easily accessible phase transitions. In this work, time-resolved X-ray diffraction, performed on perovskite cesium lead bromide nanocrystals, maps the lattice response to controlled excitation fluence. These nanocrystals undergo a reversible, photoinduced orthorhombic-to-cubic phase transition which is discernible at fluences greater than 0.34 mJ cm through the loss of orthorhombic features and shifting of high-symmetry peaks. This transition recovers on the timescale of 510 ± 100 ps. A reversible crystalline-to-amorphous transition, observable through loss of Bragg diffraction intensity, occurs at higher fluences (greater than 2.5 mJ cm). These results demonstrate that light-driven phase transitions occur in perovskite materials, which will impact optoelectronic applications and enable the manipulation of non-equilibrium phase characteristics of the broad perovskite material class.

摘要

由于铅三卤化物具有钙钛矿结构,在光伏、激光和显示应用中表现出巨大的潜力,因此人们对其产生了浓厚的兴趣。这些材料还因其不寻常的相行为而引人注目,通常表现出易于接近的相变。在这项工作中,对钙钛矿型溴化铯铅纳米晶体进行了时间分辨的 X 射线衍射,绘制了晶格对受控激发通量的响应图。这些纳米晶体经历了一个可逆的、光诱导的正交-立方相转变,在大于 0.34mJ/cm 的通量下可以通过正交特征的消失和高对称峰的移动来识别。这种转变在 510±100ps 的时间尺度上恢复。通过布拉格衍射强度的损失可以观察到在更高的通量(大于 2.5mJ/cm)下发生的可逆的晶态到非晶态的转变。这些结果表明,光驱动的相转变发生在钙钛矿材料中,这将影响光电应用,并能够操纵广泛的钙钛矿材料类别的非平衡相特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f523/6353988/6f1f2f314fd0/41467_2019_8362_Fig1_HTML.jpg

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