Kubicki Dominik J, Prochowicz Daniel, Hofstetter Albert, Ummadisingu Amita, Emsley Lyndon
School of Chemistry, University of Birmingham, B15 2TT Birmingham, U.K.
Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.
J Am Chem Soc. 2024 Apr 10;146(14):9554-9563. doi: 10.1021/jacs.3c11427. Epub 2024 Mar 28.
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 (La, Ce, Pr, Nd, Sm, Sm, Eu, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) in microcrystalline CsPbCl. Our results show that all lanthanides incorporate into the perovskite structure of CsPbCl regardless of their oxidation state (+2, +3).
镧系元素因其在可见光和近红外范围内狭窄的光发射光谱而成为光电子特性的多功能调节剂。它们在金属卤化物钙钛矿(MHP)中的应用最近备受关注,尽管它们在这些材料中的原子级命运尚未确定。我们使用铯-133固态核磁共振来确定微晶CsPbCl中所有非放射性镧系离子(La、Ce、Pr、Nd、Sm、Sm、Eu、Eu、Gd、Tb、Dy、Ho、Er、Tm、Yb、Lu)的形态。我们的结果表明,所有镧系元素都能融入CsPbCl的钙钛矿结构,无论其氧化态是+2还是+3。