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CsPbBrI纳米晶体薄膜中从光诱导相重构到卤化物偏析的转变。

Transition from Light-Induced Phase Reconstruction to Halide Segregation in CsPbBrI Nanocrystal Thin Films.

作者信息

da Cunha Thiago Rodrigues, Ferreira Diego Lourençoni, Magalhães Letícia Ferreira, de Souza Carvalho Thaís Adriany, de Souza Gabriel Fabrício, Bettini Jefferson, Faceto Angelo Danilo, Mendonça Cleber Renato, de Boni Leonardo, Schiavon Marco Antônio, Vivas Marcelo Gonçalves

机构信息

Laboratório de Espectroscopia Óptica e Fotônica, Universidade Federal de Alfenas, 37715-400 Poços de Caldas, MG, Brazil.

Grupo de Pesquisa em Química de Materiais, Universidade Federal de São João del-Rei, 36301-160 São João del-Rei, MG, Brazil.

出版信息

ACS Appl Mater Interfaces. 2025 Mar 5;17(9):14389-14403. doi: 10.1021/acsami.4c19234. Epub 2025 Feb 20.

Abstract

Inorganic metal-halide perovskite materials pave the way for many applications ranging from optoelectronics to quantum information due to their low cost, high photoluminescence and energy conversion efficiencies. However, light-induced bandgap instability due to ion migration in mixed-halide perovskites remains a significant challenge to the efficiency of optoelectronic devices. Thus, we combined hyperspectral fluorescence microspectroscopy and computational methods to understand the underlying transition mechanism between phase reconstruction and segregation in CsPbBrI (0 < < 3) nanocrystal thin films. Our outcomes have shown that samples with x = 1.0 and x = 1.5 exhibit halide migration, favoring Br enrichment locally. In this case, an interplay between photo and thermal activation promotes the expulsion of I from the perovskite lattice and generates a reconstruction of Br-rich domains, forming the CsPbBr phase. Thus, thermodynamic parameters such as the halide activation energy and phase reconstruction diffusibility were obtained by combining the kinetic parameters from linear unmixing data and Fick's second law. Moreover, we observed that the Br-I interdiffusion followed an Arrhenius-like behavior over laser-induced temperature increase. On the other hand, for samples with x = 2.0, phase segregation occurred due to the larger CsPbBrI nanocrystal size, iodine content and the high laser intensity employed. These three combined effects modify transport and recombination due to the reduction of charge carrier diffusion length (L = 10.2 nm) and bandgap. Thus, iodide ions diffuse from the nanocrystal surface to the core forming a "type-II heterostructure", promoting a red shift in the fluorescence spectrum, which is characteristic of phase segregation. Furthermore, real-time dark recovery of light-induced halide segregation is reported for CsPbBrI nanocrystal thin films. Finally, the possible halide migration mechanism and physical origins of the transition between these phenomena are pointed out.

摘要

无机金属卤化物钙钛矿材料因其低成本、高光致发光和能量转换效率,为从光电子学到量子信息等诸多应用铺平了道路。然而,混合卤化物钙钛矿中由于离子迁移导致的光致带隙不稳定性仍然是光电器件效率的重大挑战。因此,我们结合了高光谱荧光显微光谱法和计算方法,以了解CsPbBrI(0 < < 3)纳米晶体薄膜中相重构和相分离之间的潜在转变机制。我们的结果表明,x = 1.0和x = 1.5的样品表现出卤化物迁移,局部有利于Br富集。在这种情况下,光激活和热激活之间的相互作用促进了I从钙钛矿晶格中排出,并产生富含Br的区域的重构,形成CsPbBr相。因此,通过结合线性分解数据的动力学参数和菲克第二定律,获得了诸如卤化物活化能和相重构扩散率等热力学参数。此外,我们观察到在激光诱导的温度升高过程中,Br-I互扩散遵循类似阿仑尼乌斯的行为。另一方面,对于x = 2.0的样品,由于CsPbBrI纳米晶体尺寸较大、碘含量较高以及所采用的激光强度较高,发生了相分离。这三种综合效应由于载流子扩散长度(L = 10.2 nm)的减小和带隙的减小而改变了输运和复合。因此,碘离子从纳米晶体表面扩散到核心,形成“II型异质结构”,促进荧光光谱的红移,这是相分离的特征。此外,报道了CsPbBrI纳米晶体薄膜光致卤化物分离的实时暗恢复。最后,指出了这些现象之间转变的可能卤化物迁移机制和物理起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/11891859/d74ca26710ac/am4c19234_0001.jpg

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