Papadopoulou Athina, Saha Rafikul Ali, Pintor-Monroy Maria Isabel, Song Wenya, Lieberman Itai, Solano Eduardo, Roeffaers Maarten B J, Gehlhaar Robert, Genoe Jan
imec, Kapeldreef 75, Leuven 3001, Belgium.
Department of Electrical Engineering (ESAT), KU Leuven, Kasteelpark Arenberg 10, Leuven 3001, Belgium.
ACS Appl Mater Interfaces. 2024 Sep 11;16(36):47889-47901. doi: 10.1021/acsami.4c09283. Epub 2024 Aug 27.
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.
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。