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通过光谱椭偏仪研究原位退火对热共蒸发CsPbIBr薄膜的影响。

In Situ Annealing Effect on Thermally Co-Evaporated CsPbIBr Thin Films Studied via Spectroscopic Ellipsometry.

作者信息

Papadopoulou Athina, Saha Rafikul Ali, Pintor-Monroy Maria Isabel, Song Wenya, Lieberman Itai, Solano Eduardo, Roeffaers Maarten B J, Gehlhaar Robert, Genoe Jan

机构信息

imec, Kapeldreef 75, Leuven 3001, Belgium.

Department of Electrical Engineering (ESAT), KU Leuven, Kasteelpark Arenberg 10, Leuven 3001, Belgium.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 11;16(36):47889-47901. doi: 10.1021/acsami.4c09283. Epub 2024 Aug 27.

Abstract

All-inorganic cesium lead halide perovskites possess excellent thermal stability, a feature that renders them highly favorable for optoelectronic applications with an elevated thermal budget. Employing a coevaporation approach for their deposition holds promise for manufacturing at an industrial level, owing to improvements in device scalability and reproducibility. For unlocking the full potential of vacuum-evaporated perovskite thin films, it is crucial to delve deeper into their crystallization process, which, as a solid-state reaction, has been less investigated compared to the crystallization process of, most commonly used, solution-based methods. In this work, we employ spectroscopic ellipsometry, a nondestructive, high speed, and high accuracy characterization method, to study the real time annealing effect on thermally coevaporated CsPbIBr thin films in a temperature range between 25 and 300 °C. We achieve this by developing a singular dynamic model that can be fitted in real time as a function of temperature, providing insights into how thermal annealing influences the perovskite film's morphology and optical constants. Based on the latter, we derive the temperature dependence of the thermo-optic coefficient and Urbach energy as well as analyze the interband transition energies via critical point analysis. We demonstrate that the γ- to β-phase transition can be identified through a pronounced shift in the bandgap energy, whereas the β- to α-phase transition can be discerned by a sharp increase in the film's roughness. We corroborate the obtained fit results with additional in- and ex situ measurements, such as in situ grazing incidence wide-angle X-ray scattering, atomic force microscopy, reflectance/transmittance, and profilometry.

摘要

全无机铯铅卤化物钙钛矿具有出色的热稳定性,这一特性使其非常适合用于具有较高热预算的光电子应用。采用共蒸发方法沉积它们有望实现工业化生产,因为这可以提高器件的可扩展性和可重复性。为了充分发挥真空蒸发钙钛矿薄膜的潜力,深入研究其结晶过程至关重要,作为一种固态反应,与最常用的基于溶液的方法的结晶过程相比,它的研究较少。在这项工作中,我们采用光谱椭偏仪,一种无损、高速且高精度的表征方法,来研究在25至300°C温度范围内热共蒸发CsPbIBr薄膜的实时退火效果。我们通过开发一个奇异动态模型来实现这一点,该模型可以作为温度的函数实时拟合,从而深入了解热退火如何影响钙钛矿薄膜的形态和光学常数。基于此,我们推导了热光系数和乌尔巴赫能量的温度依赖性,并通过临界点分析来分析带间跃迁能量。我们证明,γ相向β相的转变可以通过带隙能量的明显变化来识别,而β相向α相的转变可以通过薄膜粗糙度的急剧增加来辨别。我们用额外的原位和非原位测量,如原位掠入射广角X射线散射、原子力显微镜、反射率/透射率和轮廓仪,来证实所获得的拟合结果。

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