Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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Eindhoven University of Technology

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2023Effect of the Precursor Chemistry on the Crystallization of Triple Cation Mixed Halide Perovskites14citations

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Slack, Jonathan L.
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Arnold, Simon
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Ceratti, Davide R.
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2023

Co-Authors (by relevance)

  • Slack, Jonathan L.
  • Arnold, Simon
  • Ceratti, Davide R.
  • Brabec, Christoph J.
  • Singh, Mriganka
  • Tao, Shuxia
  • Lee, Do Kyoung
  • Sutter-Fella, Carolin M.
  • Abdelsamie, Maged
  • Schwartz, Craig P.
  • Kodalle, Tim
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article

Effect of the Precursor Chemistry on the Crystallization of Triple Cation Mixed Halide Perovskites

  • Slack, Jonathan L.
  • Arnold, Simon
  • Ceratti, Davide R.
  • Li, Qihua
  • Brabec, Christoph J.
  • Singh, Mriganka
  • Tao, Shuxia
  • Lee, Do Kyoung
  • Sutter-Fella, Carolin M.
  • Abdelsamie, Maged
  • Schwartz, Craig P.
  • Kodalle, Tim
Abstract

Triple cation, mixed halide perovskite compositions have been reported to be more thermally stable, exhibit fewer phase impurities, and show higher power conversion efficiency and better reproducibility than single cation perovskites. In this work, we explain the formation of Cs 0.05 FA 0.81 MA 0.14 Pb(I 0.85 Br 0.15 ) 3 via a multimodal in situ study combining structural information from synchrotron grazing-incidence wide-angle X-ray scattering (GIWAXS) and optical properties from photoluminescence (PL) spectroscopy with density functional theory calculations (DFT). The focus here is on the effects of the solvent and antisolvent during crystallization. The predominantly used solvents N,N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), and the antisolvent chlorobenzene (CB) as well as the solvent-antisolvent-precursor interactions are investigated. Given the high elemental complexity and mutual interdependencies between solvent, antisolvent, and perovskite precursors, we found significant differences in the crystallization pathways. DMF-pure precursors show the formation of the DMF-containing intermediate phase and the nucleation of compositionally distinct perovskite phases, while when DMSO is added, only crystalline α- and δ-phases were found. In addition, the presence of DMSO helps the formation of α-perovskite. Coordination energy and bond order (BO) calculations support our experimental findings. Dripping of CB induces nucleation at room temperature, slows the α-phase formation rate, and appears to reduce the nucleation radius. These findings provide novel insights into solvent, antisolvent, and perovskite precursor interactions and their formation pathways. The complexity of interactions between solvents and reagents highlights the importance of understanding these effects to further improve the reproducibility and optimize processing conditions.

Topics
  • density
  • perovskite
  • impedance spectroscopy
  • photoluminescence
  • phase
  • theory
  • density functional theory
  • crystallization
  • wide-angle X-ray scattering
  • power conversion efficiency