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混合阳离子卤化物钙钛矿中相变和玻璃相特征的抑制

Suppression of phase transitions and glass phase signatures in mixed cation halide perovskites.

作者信息

Simenas Mantas, Balciunas Sergejus, Wilson Jacob N, Svirskas Sarunas, Kinka Martynas, Garbaras Andrius, Kalendra Vidmantas, Gagor Anna, Szewczyk Daria, Sieradzki Adam, Maczka Miroslaw, Samulionis Vytautas, Walsh Aron, Grigalaitis Robertas, Banys Juras

机构信息

Faculty of Physics, Vilnius University, Sauletekio 3, 10257, Vilnius, Lithuania.

Thomas Young Centre and Department of Materials, Imperial College London, SW7 2AZ, London, UK.

出版信息

Nat Commun. 2020 Oct 9;11(1):5103. doi: 10.1038/s41467-020-18938-z.

Abstract

Cation engineering provides a route to control the structure and properties of hybrid halide perovskites, which has resulted in the highest performance solar cells based on mixtures of Cs, methylammonium, and formamidinium. Here, we present a multi-technique experimental and theoretical study of structural phase transitions, structural phases and dipolar dynamics in the mixed methylammonium/dimethylammonium MADMAPbBr hybrid perovskites (0 ≤ x ≤ 1). Our results demonstrate a significant suppression of the structural phase transitions, enhanced disorder and stabilization of the cubic phase even for a small amount of dimethylammonium cations. As the dimethylammonium concentration approaches the solubility limit in MAPbBr, we observe the disappearance of the structural phase transitions and indications of a glassy dipolar phase. We also reveal a significant tunability of the dielectric permittivity upon mixing of the molecular cations that arises from frustrated electric dipoles.

摘要

阳离子工程为控制混合卤化物钙钛矿的结构和性质提供了一条途径,这已促成了基于铯、甲铵和甲脒混合物的高性能太阳能电池。在此,我们对混合甲铵/二甲铵MADMAPbBr杂化钙钛矿(0≤x≤1)中的结构相变、结构相和偶极动力学进行了多技术实验和理论研究。我们的结果表明,即使对于少量的二甲铵阳离子,结构相变也受到显著抑制,无序性增强且立方相得以稳定。当二甲铵浓度接近其在MAPbBr中的溶解度极限时,我们观察到结构相变消失以及玻璃态偶极相的迹象。我们还揭示了分子阳离子混合时介电常数的显著可调性,这源于受挫的电偶极。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f2/7547736/05d6f3e46765/41467_2020_18938_Fig1_HTML.jpg

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