Inter-Layer Diffusion of Excitations in 2D Perovskites Revealed by Photoluminescence Reabsorption

IF 19 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Functional Materials Pub Date : 2025-02-16 DOI:10.1002/adfm.202421817
Jiaxing Du, Marcello Righetto, Manuel Kober-Czerny, Siyu Yan, Karim A. Elmestekawy, Henry J. Snaith, Michael B. Johnston, Laura M. Herz
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Abstract

2D lead halide perovskites (2DPs) offer chemical compatibility with 3D perovskites and enhanced stability, which are attractive for applications in photovoltaic and light-emitting devices. However, such lowered structural dimensionality causes increased excitonic effects and highly anisotropic charge-carrier transport. Determining the diffusivity of excitations, in particular for out-of-plane or inter-layer transport, is therefore crucial, yet challenging to achieve. Here, an effective method is demonstrated for monitoring inter-layer diffusion of photoexcitations in (PEA)2PbI4 thin films by tracking time-dependent changes in photoluminescence spectra induced by photon reabsorption effects. Selective photoexcitation from either substrate- or air-side of the films reveals differences in diffusion dynamics encountered through the film profile. Time-dependent diffusion coefficients are extracted from spectral dynamics through a 1D diffusion model coupled with an interference correction for refractive index variations arising from the strong excitonic resonance of 2DPs. Such analysis, together with structural probes, shows that minute misalignment of 2DPs planes occurs at distances far from the substrate, where efficient in-plane transport consequently overshadows the less efficient out-of-plane transport in the direction perpendicular to the substrate. Through detailed analysis, a low out-of-plane excitation diffusion coefficient of (0.26 ± 0.03) ×10−4 cm2 s−1 is determined, consistent with a diffusion anisotropy of ≈4 orders of magnitude.

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光致发光重吸收揭示二维钙钛矿中激发的层间扩散
2D卤化铅钙钛矿(2DPs)与3D钙钛矿具有化学相容性和增强的稳定性,这对于光伏和发光器件的应用具有吸引力。然而,这种降低的结构维度导致了激子效应的增加和高度各向异性的载流子输运。因此,确定激发的扩散率,特别是对于面外或层间传输,是至关重要的,但很难实现。本文提出了一种监测(PEA)2PbI4薄膜中光激发层间扩散的有效方法,即跟踪光子重吸收效应引起的光致发光光谱的随时间变化。薄膜的衬底侧或空气侧的选择性光激发揭示了通过薄膜剖面遇到的扩散动力学的差异。时间相关的扩散系数通过一维扩散模型从光谱动力学中提取,并对由2dp的强激子共振引起的折射率变化进行干涉校正。这种分析与结构探针一起表明,在远离衬底的距离处,2dp平面的微小错位发生,在那里,有效的面内传输因此掩盖了垂直于衬底方向上效率较低的面外传输。通过详细分析,确定了低的面外激发扩散系数为(0.26±0.03)×10−4 cm2 s−1,与≈4个数量级的扩散各向异性相一致。
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来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
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