UC Berkeley

Paramagnetic solid-state NMR of lanthanide (Ln) containing materials can be challenging due to the high electron spin states possible for the Ln f electrons, which result in large paramagnetic shifts, and these difficulties are compounded for ¹⁷O due to the low natural abundance and quadrupolar character. In this work, we present examples of ¹⁷O NMR experiments for lanthanide oxides and strategies to overcome these difficulties. In particular, we record and assign the ¹⁷O NMR spectra of monoclinic Sm₂O₃ and Eu₂O₃ for the first time, as well as performing density functional theory (DFT) calculations to gain further insight into the spectra. The temperature dependence of the Sm³⁺ and Eu³⁺ magnetic susceptibilities are investigated by measuring the ¹⁷O shift of the cubic sesquioxides over a wide temperature range, which reveal non-Curie temperature dependence due to the presence of low-lying electronic states. This behaviour is reproduced by calculating the electron spin as a function of temperature, yielding shifts which agree well with the experimental values. Using the understanding of the magnetic behaviour gained from the sesquioxides, we then explore the local oxygen environments in 15 at% Sm- and Eu-substituted CeO₂, with the ¹⁷O NMR spectrum exhibiting signals due to environments with zero, one and two nearest neighbour Ln ions, as well as further splitting due to oxygen vacancies. Finally, we extract an activation energy for oxygen vacancy motion in these systems of 0.35 ± 0.02 eV from the Arrhenius temperature dependence of the ¹⁷O T₁ relaxation constants, which is found to be independent of the Ln ion within error. The relation of this activation energy to literature values for oxygen diffusion in Ln-substituted CeO₂ is discussed to infer mechanistic information which can be applied to further develop these materials as solid-state oxide-ion conductors.