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Surface Passivation Suppresses Local Ion Motion in Halide Perovskites.
Pothoof, Justin; Westbrook, Robert J E; Giridharagopal, Rajiv; Breshears, Madeleine D; Ginger, David S.
Afiliação
  • Pothoof J; Department of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195-1700, United States.
  • Westbrook RJE; Department of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195-1700, United States.
  • Giridharagopal R; Department of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195-1700, United States.
  • Breshears MD; Department of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195-1700, United States.
  • Ginger DS; Department of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195-1700, United States.
J Phys Chem Lett ; 14(26): 6092-6098, 2023 Jul 06.
Article em En | MEDLINE | ID: mdl-37364056
ABSTRACT
We use scanning probe microscopy to study ion migration in formamidinium (FA)-containing halide perovskite semiconductor Cs0.22FA0.78Pb(I0.85Br0.15)3 in the presence and absence of chemical surface passivation. We measure the evolving contact potential difference (CPD) using scanning Kelvin probe microscopy (SKPM) following voltage poling. We find that ion migration leads to a ∼100 mV shift in the CPD of control films after poling with 3 V for only a few seconds. Moreover, we find that ion migration is heterogeneous, with domain interfaces leading to a larger CPD shift than domain interiors. Application of (3-aminopropyl)trimethoxysilane (APTMS) as a surface passivator further leads to 5-fold reduction in the CPD shift from ∼100 to ∼20 mV. We use hyperspectral microscopy to confirm that APTMS-treated perovskite films undergo less photoinduced halide migration than control films. We interpret these results as due to a reduction in the halide vacancy concentration after APTMS passivation.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2023 Tipo de documento: Article