García-Benito Inés, Quarti Claudio, Queloz Valentin I E, Hofstetter Yvonne J, Becker-Koch David, Caprioglio Pietro, Neher Dieter, Orlandi Simonetta, Cavazzini Marco, Pozzi Gianluca, Even Jacky, Nazeeruddin Mohammad Khaja, Vaynzof Yana, Grancini Giulia
Group for Molecular Engineering of Functional Materials, Institute of Chemical Sciences and Engineering, EPFL Valais Wallis, Sion, Switzerland.
Laboratory for Chemistry of Novel Materials, Department of Chemistry, Université de Mons, Mons, Belgium.
Front Chem. 2020 Jan 28;7:946. doi: 10.3389/fchem.2019.00946. eCollection 2019.
Low-dimensional hybrid perovskites have triggered significant research interest due to their intrinsically tunable optoelectronic properties and technologically relevant material stability. In particular, the role of the organic spacer on the inherent structural and optical features in two-dimensional (2D) perovskites is paramount for material optimization. To obtain a deeper understanding of the relationship between spacers and the corresponding 2D perovskite film properties, we explore the influence of the partial substitution of hydrogen atoms by fluorine in an alkylammonium organic cation, resulting in (Lc)PbI and (Lf)PbI 2D perovskites, respectively. Consequently, optical analysis reveals a clear 0.2 eV blue-shift in the excitonic position at room temperature. This result can be mainly attributed to a band gap opening, with negligible effects on the exciton binding energy. According to Density Functional Theory (DFT) calculations, the band gap increases due to a larger distortion of the structure that decreases the atomic overlap of the wavefunctions and correspondingly bandwidth of the valence and conduction bands. In addition, fluorination impacts the structural rigidity of the 2D perovskite, resulting in a stable structure at room temperature and the absence of phase transitions at a low temperature, in contrast to the widely reported polymorphism in some non-fluorinated materials that exhibit such a phase transition. This indicates that a small perturbation in the material structure can strongly influence the overall structural stability and related phase transition of 2D perovskites, making them more robust to any phase change. This work provides key information on how the fluorine content in organic spacer influence the structural distortion of 2D perovskites and their optical properties which possess remarkable importance for future optoelectronic applications, for instance in the field of light-emitting devices or sensors.
低维混合钙钛矿因其固有的可调节光电特性和与技术相关的材料稳定性而引发了广泛的研究兴趣。特别是,有机间隔基团对二维(2D)钙钛矿固有结构和光学特性的作用对于材料优化至关重要。为了更深入地理解间隔基团与相应二维钙钛矿薄膜特性之间的关系,我们研究了在烷基铵有机阳离子中用氟部分取代氢原子的影响,分别得到了(Lc)PbI和(Lf)PbI二维钙钛矿。因此,光学分析表明室温下激子位置有明显的0.2 eV蓝移。这一结果主要归因于带隙的打开,而对激子结合能的影响可忽略不计。根据密度泛函理论(DFT)计算,带隙增加是由于结构的更大畸变,这降低了波函数的原子重叠以及价带和导带相应的带宽。此外,氟化影响二维钙钛矿的结构刚性,导致在室温下结构稳定且在低温下无相变,这与一些非氟化材料中广泛报道的多晶型现象形成对比,后者会出现这种相变。这表明材料结构中的微小扰动会强烈影响二维钙钛矿的整体结构稳定性和相关相变,使其对任何相变更具抗性。这项工作提供了关键信息,即有机间隔基团中的氟含量如何影响二维钙钛矿的结构畸变及其光学特性,这对于未来的光电应用,例如发光器件或传感器领域,具有重要意义。