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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2016High Chloride Doping Levels Stabilize the Perovskite Phase of Cesium Lead Iodide273citations

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Chart of shared publication
Egger, David A.
1 / 9 shared
Liu, Shi
1 / 1 shared
Dillon, Andrew D.
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Tan, Liang Z.
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Fafarman, Aaron T.
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Rappe, Andrew M.
1 / 11 shared
Kronik, Leeor
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Dastidar, Subham
1 / 2 shared
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2016

Co-Authors (by relevance)

  • Egger, David A.
  • Liu, Shi
  • Dillon, Andrew D.
  • Tan, Liang Z.
  • Fafarman, Aaron T.
  • Rappe, Andrew M.
  • Kronik, Leeor
  • Dastidar, Subham
OrganizationsLocationPeople

article

High Chloride Doping Levels Stabilize the Perovskite Phase of Cesium Lead Iodide

  • Cromer, Samuel B.
  • Egger, David A.
  • Liu, Shi
  • Dillon, Andrew D.
  • Tan, Liang Z.
  • Fafarman, Aaron T.
  • Rappe, Andrew M.
  • Kronik, Leeor
  • Dastidar, Subham
Abstract

<p>Cesium lead iodide possesses an excellent combination of band gap and absorption coefficient for photovoltaic applications in its perovskite phase. However, this is not its equilibrium structure under ambient conditions. In air, at ambient temperature it rapidly transforms to a nonfunctional, so-called yellow phase. Here we show that chloride doping, particularly at levels near the solubility limit for chloride in a cesium lead iodide host, provides a new approach to stabilizing the functional perovskite phase. In order to achieve high doping levels, we first co-deposit colloidal nanocrystals of pure cesium lead chloride and cesium lead iodide, thereby ensuring nanometer-scale mixing even at compositions that potentially exceed the bulk miscibility of the two phases. The resulting nanocrystal solid is subsequently fused into a polycrystalline thin film by chemically induced, room-temperature sintering. Spectroscopy and X-ray diffraction indicate that the chloride is further dispersed during sintering and a polycrystalline mixed phase is formed. Using density functional theory (DFT) methods in conjunction with nudged elastic band techniques, low-energy pathways for interstitial chlorine diffusion into a majority-iodide lattice were identified, consistent with the facile diffusion and fast halide exchange reactions observed. By comparison to DFT-calculated values (with the PBE exchange-correlation functional), the relative change in band gap and the lattice contraction are shown to be consistent with a Cl/I ratio of a few percent in the mixed phase. At these incorporation levels, the half-life of the functional perovskite phase in a humid atmosphere increases by more than an order of magnitude.</p>

Topics
  • density
  • perovskite
  • impedance spectroscopy
  • phase
  • x-ray diffraction
  • theory
  • thin film
  • density functional theory
  • interstitial
  • sintering