Gao Lili, Li Xiaotong, Traoré Boubacar, Zhang Yalan, Fang Junjie, Han Yu, Even Jacky, Katan Claudine, Zhao Kui, Liu Shengzhong, Kanatzidis Mercouri G
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, Shaanxi Key Laboratory for Advanced Energy Devices, Shaanxi Engineering Lab for Advanced Energy Technology, Institute for Advanced Energy Materials, School of Materials Science and Engineering, Shaanxi Normal University, Xi'an 710119, China.
Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.
J Am Chem Soc. 2021 Aug 11;143(31):12063-12073. doi: 10.1021/jacs.1c03687. Epub 2021 Aug 3.
Two-dimensional (2D) halide perovskites have several distinct structural classes and exhibit great tunability, stability, and high potential for photovoltaic applications. Here, we report a new series of hybrid 2D perovskites in the Dion-Jacobson (DJ) class based on aromatic -phenylenediammonium (mPDA) dications. The crystal structures of the DJ perovskite materials (mPDA)MAPbI ( = 1-3) were solved and refined using single-crystal X-ray crystallography. The results indicate a short I···I interlayer distance of 4.00-4.04 Å for the (mPDA)MAPbI ( = 2 and 3) structures, which is the shortest among DJ perovskites. However, Pb-I-Pb angles are as small as 158-160°, reflecting the large distortion of the inorganic framework, which results in larger band gaps for these materials than those in other DJ analogues. Density functional theory calculations suggest appreciable dispersion in the stacking direction, unlike the band structures of the Ruddlesden-Popper phases, which exhibit flat bands along the stacking direction. This is a consequence of the short interlayer I···I distances that can lead to interlayer electronic coupling across the layers. The solution-deposited films (nominal (mPDA)MAPbI compositions of = 1-6) reveal improved surface coverage with increasing nominal value with the higher films being composed of a mixture of = 1 and bulk three-dimensional MAPbI perovskites. The films made from solutions of these materials behave differently from those of other 2D iodide perovskites, and their solar cells have a mixture of = 1 DJ and MAPbI as light-absorbing semiconductors.
二维(2D)卤化物钙钛矿具有几种不同的结构类型,并展现出极大的可调控性、稳定性以及在光伏应用方面的巨大潜力。在此,我们报道了基于芳族 - 苯二铵(mPDA)双阳离子的狄翁 - 雅各布森(DJ)类新型混合2D钙钛矿系列。利用单晶X射线晶体学解析并精修了DJ钙钛矿材料(mPDA)MAPbI₃(n = 1 - 3)的晶体结构。结果表明,(mPDA)MAPbI₃(n = 2和3)结构的I···I层间距离短至4.00 - 4.04 Å,这是DJ钙钛矿中最短的。然而,Pb - I - Pb角小至158 - 160°,反映出无机骨架的大畸变,这导致这些材料的带隙比其他DJ类似物的带隙更大。密度泛函理论计算表明,与沿堆叠方向呈现平带的Ruddlesden - Popper相的能带结构不同,在堆叠方向上存在可观的色散。这是层间I···I距离短的结果,其可导致跨层的层间电子耦合。溶液沉积膜(标称(mPDA)MAPbI₃组成n = 1 - 6)显示,随着标称n值增加,表面覆盖率提高,较高n值的膜由n = 1和体相三维MAPbI₃钙钛矿的混合物组成。由这些材料溶液制成的膜与其他2D碘化物钙钛矿的膜表现不同,并且它们的太阳能电池具有n = 1的DJ和MAPbI₃作为吸光半导体的混合物。