2D Halide Perovskite Phase Formation Dynamics and Their Regulation by Co‐Additives for Efficient Solar Cells

Abstract The incorporation of large organic ammonium ions renders the crystallization dynamics and layer formation process of halide perovskites complex, difficult to control, and leads to problems of suppressed charge transport with the formation of tiny‐sized grains. In this paper, the use of meth...

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Main Authors: Min Liu, Daming Zheng, Tao Zhu, Karol Vegso, Peter Siffalovic, Thierry Pauporté
Format: Article
Language:English
Published: Wiley-VCH 2024-02-01
Series:Advanced Materials Interfaces
Subjects:
Online Access:https://doi.org/10.1002/admi.202300773
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author Min Liu
Daming Zheng
Tao Zhu
Karol Vegso
Peter Siffalovic
Thierry Pauporté
author_facet Min Liu
Daming Zheng
Tao Zhu
Karol Vegso
Peter Siffalovic
Thierry Pauporté
author_sort Min Liu
collection DOAJ
description Abstract The incorporation of large organic ammonium ions renders the crystallization dynamics and layer formation process of halide perovskites complex, difficult to control, and leads to problems of suppressed charge transport with the formation of tiny‐sized grains. In this paper, the use of methylammonium chloride (MACl) and an excess of PbI2 is introduced as a co‐additives in the precursor solution for the control of phenylmethylammonium or benzylammonium (PMA+ spacer) and formamidinium (FA+)‐based quasi‐2D PMA2FAn−1PbnI3n+1 (n = 5) perovskite layers formation. By this method, the morphology of the layer, the inner phase distribution, and the charge transport properties are improved. By employing glow discharge‐optical emission spectroscopy (GD‐OES) and other techniques, it is revealed that the quasi‐2D perovskites prepared in the presence of co‐additives exhibit uniform removal dynamics of the solvent across the film. Furthermore, the grain growth mode, upon thermal annealing, is lateral. It results in large, monolithic grains with low‐trap state density and excellent substrate coverage. Particularly, co‐additives improve the cations dispersion upon the crystallization process, thus suppressing the low‐n phase formed through the aggregation of spacer cations and accelerating the formation of the high‐n phase.
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spelling doaj.art-f6a5278da441421f838fee4f35fab2012024-02-24T04:11:01ZengWiley-VCHAdvanced Materials Interfaces2196-73502024-02-01116n/an/a10.1002/admi.2023007732D Halide Perovskite Phase Formation Dynamics and Their Regulation by Co‐Additives for Efficient Solar CellsMin Liu0Daming Zheng1Tao Zhu2Karol Vegso3Peter Siffalovic4Thierry Pauporté5Chimie ParisTech PSL Research University CNRS Institut de Recherche de Chimie Paris (IRCP) UMR8247, 11 rue P. et M. Curie Paris F‐75005 FranceChimie ParisTech PSL Research University CNRS Institut de Recherche de Chimie Paris (IRCP) UMR8247, 11 rue P. et M. Curie Paris F‐75005 FranceChimie ParisTech PSL Research University CNRS Institut de Recherche de Chimie Paris (IRCP) UMR8247, 11 rue P. et M. Curie Paris F‐75005 FranceInstitute of Physics Slovak Academy of Sciences Dubravska cesta 9 Bratislava 84511 SlovakiaInstitute of Physics Slovak Academy of Sciences Dubravska cesta 9 Bratislava 84511 SlovakiaChimie ParisTech PSL Research University CNRS Institut de Recherche de Chimie Paris (IRCP) UMR8247, 11 rue P. et M. Curie Paris F‐75005 FranceAbstract The incorporation of large organic ammonium ions renders the crystallization dynamics and layer formation process of halide perovskites complex, difficult to control, and leads to problems of suppressed charge transport with the formation of tiny‐sized grains. In this paper, the use of methylammonium chloride (MACl) and an excess of PbI2 is introduced as a co‐additives in the precursor solution for the control of phenylmethylammonium or benzylammonium (PMA+ spacer) and formamidinium (FA+)‐based quasi‐2D PMA2FAn−1PbnI3n+1 (n = 5) perovskite layers formation. By this method, the morphology of the layer, the inner phase distribution, and the charge transport properties are improved. By employing glow discharge‐optical emission spectroscopy (GD‐OES) and other techniques, it is revealed that the quasi‐2D perovskites prepared in the presence of co‐additives exhibit uniform removal dynamics of the solvent across the film. Furthermore, the grain growth mode, upon thermal annealing, is lateral. It results in large, monolithic grains with low‐trap state density and excellent substrate coverage. Particularly, co‐additives improve the cations dispersion upon the crystallization process, thus suppressing the low‐n phase formed through the aggregation of spacer cations and accelerating the formation of the high‐n phase.https://doi.org/10.1002/admi.202300773additive compoundscrystallization mechanismphase distributionRudlesden–Popper 2D perovskitesolar cells
spellingShingle Min Liu
Daming Zheng
Tao Zhu
Karol Vegso
Peter Siffalovic
Thierry Pauporté
2D Halide Perovskite Phase Formation Dynamics and Their Regulation by Co‐Additives for Efficient Solar Cells
Advanced Materials Interfaces
additive compounds
crystallization mechanism
phase distribution
Rudlesden–Popper 2D perovskite
solar cells
title 2D Halide Perovskite Phase Formation Dynamics and Their Regulation by Co‐Additives for Efficient Solar Cells
title_full 2D Halide Perovskite Phase Formation Dynamics and Their Regulation by Co‐Additives for Efficient Solar Cells
title_fullStr 2D Halide Perovskite Phase Formation Dynamics and Their Regulation by Co‐Additives for Efficient Solar Cells
title_full_unstemmed 2D Halide Perovskite Phase Formation Dynamics and Their Regulation by Co‐Additives for Efficient Solar Cells
title_short 2D Halide Perovskite Phase Formation Dynamics and Their Regulation by Co‐Additives for Efficient Solar Cells
title_sort 2d halide perovskite phase formation dynamics and their regulation by co additives for efficient solar cells
topic additive compounds
crystallization mechanism
phase distribution
Rudlesden–Popper 2D perovskite
solar cells
url https://doi.org/10.1002/admi.202300773
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