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Light-Induced Halide Segregation in 2D and Quasi-2D Mixed-Halide Perovskites AITranslate

Eindhoven University of Technology; Eindhoven University of Technology;Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne; Eindhoven University of Technology;Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne;Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne; Eindhoven University of Technology;Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne; Eindhoven University of Technology; Eindhoven University of Technology
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Publisher: ACS
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Abstract AITranslate

Photoinduced halide segregation hinders widespread application of three-dimensional (3D) mixed-halide perovskites. Much less is known about this phenomenon in lower-dimensional systems. Here, we study photoinduced halide segregation in lower-dimensional mixed iodide-bromide perovskites (PEA2MAn–1Pbn(BrxI1–x)3n+1, with PEA+: phenethylammonium and MA+: methylammonium) through time-dependent photoluminescence (PL) spectroscopy. We show that layered two-dimensional (2D) structures render additional stability against the demixing of halide phases under illumination. We ascribe this behavior to reduced halide mobility due to the intrinsic heterogeneity of 2D mixed-halide perovskites, which we demonstrate via 207Pb solid-state NMR. However, the dimensionality of the 2D phase is critical in regulating photostability. By tracking the PL of multidimensional perovskite films under illumination, we find that while halide segregation is largely inhibited in 2D perovskites (n = 1), it is not suppressed in quasi-2D phases (n = 2), which display a behavior intermediate between 2D and 3D and a peculiar absence of halide redistribution in the dark that is only induced at higher temperature for the quasi-2D phase.

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DOI:https://doi.org/10.1021/acsenergylett.3c00160

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Citation Information:

Photoinduced halide segregation hinders widespread application of three-dimensional (3D) mixed-halide perovskites. Much less is known about this phenomenon in lower-dimensional systems. Here, we study photoinduced halide segregation in lower-dimensional mixed iodide-bromide perovskites (PEA2MAn–1Pbn(BrxI1–x)3n+1, with PEA+: phenethylammonium and MA+: methylammonium) through time-dependent photoluminescence (PL) spectroscopy. We show that layered two-dimensional (2D) structures render additional stability against the demixing of halide phases under illumination. We ascribe this behavior to reduced halide mobility due to the intrinsic heterogeneity of 2D mixed-halide perovskites, which we demonstrate via 207Pb solid-state NMR. However, the dimensionality of the 2D phase is critical in regulating photostability. By tracking the PL of multidimensional perovskite films under illumination, we find that while halide segregation is largely inhibited in 2D perovskites (n = 1), it is not suppressed in quasi-2D phases (n = 2), which display a behavior intermediate between 2D and 3D and a peculiar absence of halide redistribution in the dark that is only induced at higher temperature for the quasi-2D phase.

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GB/T 7714-2015 [1] Kunal Datta, Alessandro Caiazzo, Michael A. Hope, et al. ACS Energy Letters, 2023(8). DOI:10.1021/acsenergylett.3c00160.
MLA [1] Kunal Datta, et al., ACS Energy Letters, no. 8, 2023, https://doi.org/10.1021/acsenergylett.3c00160.
APA [1] Kunal Datta, Alessandro Caiazzo, Michael A. Hope, Junyu Li, Aditya Mishra, Manuel Cordova, Zehua Chen, Lyndon Emsley, Martijn M. Wienk, & René A. J. Janssen. (2023). ACS Energy Letters(8). https://doi.org/10.1021/acsenergylett.3c00160
IEEE [1] Kunal Datta, Alessandro Caiazzo, Michael A. Hope, Junyu Li, Aditya Mishra, Manuel Cordova, Zehua Chen, Lyndon Emsley, Martijn M. Wienk, and René A. J. Janssen, ACS Energy Letters, no. 8, 2023, doi: 10.1021/acsenergylett.3c00160.