Eledath-Changarath Mahesh, Gualdrón-Reyes Andrés F, Rodríguez-Romero Jesús, Mora-Seró Iván, Suárez Isaac, Canet-Albiach Rodolfo, Asensio Maria C, P Martínez-Pastor Juan, Boichuk Andrii, Boichuk Tetiana, Sánchez-Royo Juan F, Krečmarová Marie
Instituto de Ciencia de Materiales, Universidad de Valencia (ICMUV), Valencia 46071, Spain.
Institute of Advanced Materials (INAM), Universitat Jaume I, Castellón 12006, Spain.
ACS Appl Mater Interfaces. 2024 Nov 20;16(46):64123-64135. doi: 10.1021/acsami.4c11096. Epub 2024 Nov 5.
Two-dimensional halide perovskites are promising for advanced photonic, optoelectronic, and photovoltaic applications. However, their long-term stability is still a critical factor limiting their implementation into further commercial applications. Here, we present an environmental stability analysis of BA(MA)PbI (BA = CHN, MA = CHN) two-dimensional perovskites with the lowest quantum well thicknesses of = 1 and = 2, after 1 year of aging under ambient humidity, oxygen content, and light conditions. We observed that both crystal phases ( = 1 and 2) degraded similarly, resulting in the removal of organic components and crystal decomposition into PbI, Pb oxides, and Pb hydroxides. However, we have found a significant difference between their aging under ambient light and dark conditions, affecting their degraded morphology and photoactivity. Both crystal phases exposed to ambient light aged into a morphology characterized by the formation of several pinholes and voids, accompanied by photoluminescence degradation. Samples stored under dark conditions surprisingly preserved their photoluminescence activity, which morphologically aged into microrod structures. We conclude that the observed loss of photoactivity of 2D perovskites aged under ambient light is attributed to photoaccelerated degradation processes causing faster crystal surface photo-oxidation accompanied by a creation of multiple I vacancies and hydration of the inner crystal. The retainment of photoactivity in 2D perovskites aged under dark conditions is attributed to slower surface oxidation processes into Pb salts, as confirmed by X-ray photoemission spectroscopy. The formed surface layer even allows for a layer-by-layer degradation and acts as a protection barrier against further additional loss of I atoms and the consequent hydration of the inner part of samples. We demonstrate that light is the most critical external factor accelerating 2D perovskite degradation processes in ambient air and thus affecting their long-term stability. We conclude in this work that perovskite material structural engineering together with their surface passivation or encapsulation strategical techniques applied is an essential step for their further application into long-term stable commercial devices.
二维卤化物钙钛矿在先进的光子、光电子和光伏应用中具有广阔前景。然而,它们的长期稳定性仍是限制其进一步商业化应用的关键因素。在此,我们展示了在环境湿度、氧气含量和光照条件下老化1年后,量子阱厚度最低分别为 = 1和 = 2的BA(MA)PbI(BA = CHN,MA = CHN)二维钙钛矿的环境稳定性分析。我们观察到两种晶相( = 1和 = 2)的降解情况相似,导致有机成分去除,晶体分解为PbI、Pb氧化物和Pb氢氧化物。然而,我们发现它们在环境光照和黑暗条件下老化存在显著差异,这影响了它们的降解形态和光活性。暴露在环境光下的两种晶相老化后形成的形态特征是出现多个针孔和空隙,同时伴随着光致发光降解。在黑暗条件下储存的样品出人意料地保留了其光致发光活性,其形态老化为微棒结构。我们得出结论,在环境光下老化的二维钙钛矿观察到的光活性损失归因于光加速降解过程,该过程导致晶体表面更快的光氧化,同时产生多个I空位并使内部晶体水合。黑暗条件下老化的二维钙钛矿光活性的保留归因于向Pb盐的较慢表面氧化过程,这通过X射线光电子能谱得到证实。形成表面层甚至允许逐层降解,并作为防止样品内部进一步额外损失I原子和随之而来的水合作用的保护屏障。我们证明,光是加速二维钙钛矿在环境空气中降解过程并因此影响其长期稳定性最关键的外部因素。我们在这项工作中得出结论,钙钛矿材料结构工程及其表面钝化或封装策略技术的应用是其进一步应用于长期稳定商业器件的关键步骤。