分子升华使定向FAPbI3钙钛矿实现2D-3D转化

0 CHEMISTRY, MULTIDISCIPLINARY
Zihui Liang, Jinguo Cao, Zezhu Zhou, Lizhi Ren, Haodong Wu, Zhen Wang, Changhai Yi, Dong Yang, Kai Wang, Congcong Wu
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引用次数: 0

摘要

晶体面的精确排列和战略性定位对于提高钙钛矿材料的稳定性和光伏效率至关重要。然而,由于传统方法中溶剂去除后随机成核以及随之而来的不可控晶体生长,优选面取向的合成和生长机制的解构是具有挑战性的。为了减轻溶剂诱导的无序效应,本文介绍了一种涉及二维(2D)层状钙钛矿的方法,该方法在分子升华时启动晶体学控制的晶格生长。这种直接的全固体合成途径被称为“2D-to-3D (α)”,是传统的“δ-to-α”相变途径的补充。高取向α-甲脒碘化铅(α-FAPbI3)钙钛矿薄膜的生长具有精确控制面排列和最小化晶格失配的特点。太阳能电池效率达到25.01%,该方法为钙钛矿太阳能电池的升级到组件级制造提供了优势,在70平方厘米的有效面积上,效率超过20%。由于随机成核,具有优选面取向的钙钛矿材料的合成具有挑战性。本文合成了一种二维层状钙钛矿,该层状钙钛矿在分子升华后引发可控的晶格生长,使α-FAPbI3钙钛矿形成具有长程晶格有序的大面积薄膜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular sublimation enables 2D–3D transformation of orientational FAPbI3 perovskites

Molecular sublimation enables 2D–3D transformation of orientational FAPbI3 perovskites
The precise alignment and strategic positioning of crystal facets are essential for enhancing the stability and photovoltaic efficacy of perovskite materials. However, the synthesis of preferred facet orientations and the deconstruction of growth mechanisms are challenging due to randomized nucleation upon solvent removal and the consequent uncontrollable crystalline growth in traditional approaches. To mitigate solvent-induced disorder effects, here we introduce an approach involving a two-dimensional (2D) layered perovskite that initiates crystallographically controlled lattice growth upon molecular sublimation. This direct all-solid synthetic pathway is termed ‘2D-to-3D (α)’ and complements the traditional ‘δ-to-α’ phase transformation route. The growth of highly oriented α-formamidinium lead iodide (α-FAPbI3) perovskite films is facilitated, characterized by precise control over facet alignment and minimized lattice mismatch. A solar cell efficiency of 25.01% is achieved and the method offers advantages for the upscaling of perovskite solar cells to module-level manufacturing, demonstrating an efficiency of over 20% for an active area of 70 cm2. The synthesis of perovskite materials with preferred facet orientations is challenging due to randomized nucleation. Here a two-dimensional layered perovskite that initiates controlled lattice growth upon molecular sublimation is synthesized, enabling the formation of large-area films of α-FAPbI3 perovskite with long-range lattice order.
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