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Speciation of Lanthanide Metal Ion Dopants in Microcrystalline All-Inorganic Halide Perovskite CsPbCl3.
Kubicki, Dominik J; Prochowicz, Daniel; Hofstetter, Albert; Ummadisingu, Amita; Emsley, Lyndon.
  • Kubicki DJ; School of Chemistry, University of Birmingham, B15 2TT Birmingham, U.K.
  • Prochowicz D; Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.
  • Hofstetter A; Laboratory of Magnetic Resonance, Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.
  • Ummadisingu A; Manufacturing Futures Laboratory, Department of Chemical Engineering, University College London, Torrington Place, WC1E 7JE London, United Kingdom.
  • Emsley L; Laboratory of Magnetic Resonance, Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.
J Am Chem Soc ; 146(14): 9554-9563, 2024 Apr 10.
Article en En | MEDLINE | ID: mdl-38548624
ABSTRACT
Lanthanides are versatile modulators of optoelectronic properties owing to their narrow optical emission spectra across the visible and near-infrared range. Their use in metal halide perovskites (MHPs) has recently gained prominence, although their fate in these materials has not yet been established at the atomic level. We use cesium-133 solid-state NMR to establish the speciation of all nonradioactive lanthanide ions (La3+, Ce3+, Pr3+, Nd3+, Sm3+, Sm2+, Eu3+, Eu2+, Gd3+, Tb3+, Dy3+, Ho3+, Er3+, Tm3+, Yb3+, Lu3+) in microcrystalline CsPbCl3. Our results show that all lanthanides incorporate into the perovskite structure of CsPbCl3 regardless of their oxidation state (+2, +3).