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.

Vertically aligned nanocomposite (VAN) films, comprising nanopillars of one phase embedded in a matrix of another, have shown great promise for a range of applications due to their high interfacial areas oriented perpendicular to the substrate. In particular, oxide VANs show enhanced oxide-ion conductivity in directions that are orthogonal to those found in more conventional thin-film heterostructures; however, the structure of the interfaces and its influence on conductivity remain unclear. In this work, ¹⁷O NMR spectroscopy is used to study CeO₂-SrTiO₃ VAN thin films: selective isotopic enrichment is combined with a lift-off technique to remove the substrate, facilitating detection of the ¹⁷O NMR signal from single atomic layer interfaces. By performing the isotopic enrichment at variable temperatures, the superior oxide-ion conductivity of the VAN films compared to the bulk materials is shown to arise from enhanced oxygen mobility at this interface; oxygen motion at the interface is further identified from ¹⁷O relaxometry experiments. The structure of this interface is solved by calculating the NMR parameters using density functional theory combined with random structure searching, allowing the chemistry underpinning the enhanced oxide-ion transport to be proposed. Finally, a comparison is made with 1% Gd-doped CeO₂-SrTiO₃ VAN films, for which greater NMR signal can be obtained due to paramagnetic relaxation enhancement, while the relative oxide-ion conductivities of the phases remain similar. These results highlight the information that can be obtained on interfacial structure and dynamics with solid-state NMR spectroscopy, in this and other nanostructured systems, our methodology being generally applicable to overcome sensitivity limitations in thin-film studies.

While solid-state NMR spectroscopic techniques have helped clarify the local structure and dynamics of ionic conductors, similar studies of mixed ionic-electronic conductors (MIECs) have been hampered by the paramagnetic behavior of these systems. Here we report high-resolution (17)O (I = 5/2) solid-state NMR spectra of the mixed-conducting solid oxide fuel cell (SOFC) cathode material La2NiO4+δ, a paramagnetic transition-metal oxide. Three distinct oxygen environments (equatorial, axial, and interstitial) can be assigned on the basis of hyperfine (Fermi contact) shifts and quadrupolar nutation behavior, aided by results from periodic DFT calculations. Distinct structural distortions among the axial sites, arising from the nonstoichiometric incorporation of interstitial oxygen, can be resolved by advanced magic angle turning and phase-adjusted sideband separation (MATPASS) NMR experiments. Finally, variable-temperature spectra reveal the onset of rapid interstitial oxide motion and exchange with axial sites at ∼130 °C, associated with the reported orthorhombic-to-tetragonal phase transition of La2NiO4+δ. From the variable-temperature spectra, we develop a model of oxide-ion dynamics on the spectral time scale that accounts for motional differences of all distinct oxygen sites. Though we treat La2NiO4+δ as a model system for a combined paramagnetic (17)O NMR and DFT methodology, the approach presented herein should prove applicable to MIECs and other functionally important paramagnetic oxides.

Large-scale electric energy storage is fundamental to the use of renewable energy. Recently, research and development efforts on room-temperature sodium-ion batteries (NIBs) have been revitalized, as NIBs are considered promising, low-cost alternatives to the current Li-ion battery technology for large-scale applications. Herein, we introduce a novel layered oxide cathode material, Na_0.78Ni_0.23Mn_0.69O₂. This new compound provides a high reversible capacity of 138 mAh g^-1 and an average potential of 3.25 V vs Na⁺/Na with a single smooth voltage profile. Its remarkable rate and cycling performances are attributed to the elimination of the P2-O2 phase transition upon cycling to 4.5 V. The first charge process yields an abnormally excess capacity, which has yet to be observed in other P2 layered oxides. Metal K-edge XANES results show that the major charge compensation at the metal site during Na-ion deintercalation is achieved via the oxidation of nickel (Ni²⁺) ions, whereas, to a large extent, manganese (Mn) ions remain in their Mn⁴⁺ state. Interestingly, electron energy loss spectroscopy (EELS) and soft X-ray absorption spectroscopy (sXAS) results reveal differences in electronic structures in the bulk and at the surface of electrochemically cycled particles. At the surface, transition metal ions (TM ions) are in a lower valence state than in the bulk, and the O K-edge prepeak disappears. On the basis of previous reports on related Li-excess LIB cathodes, it is proposed that part of the charge compensation mechanism during the first cycle takes place at the lattice oxygen site, resulting in a surface to bulk transition metal gradient. We believe that by optimizing and controlling oxygen activity, Na layered oxide materials with higher capacities can be designed.

Hybrid organic-inorganic perovskites represent a special class of metal-organic framework where a molecular cation is encased in an anionic cage. The molecule-cage interaction influences phase stability, phase transformations, and the molecular dynamics. We examine the hydrogen bonding in four AmBX₃ formate perovskites: [Am]Zn(HCOO)₃, with Am⁺ = hydrazinium (NH₂NH₃⁺), guanidinium (C(NH₂)₃⁺), dimethylammonium (CH₃)₂NH₂⁺, and azetidinium (CH₂)₃NH₂⁺. We develop a scheme to quantify the strength of hydrogen bonding in these systems from first-principles, which separates the electrostatic interactions between the amine (Am⁺) and the BX₃^- cage. The hydrogen-bonding strengths of formate perovskites range from 0.36 to 1.40 eV/cation (8-32 kcalmol^-1). Complementary solid-state nuclear magnetic resonance spectroscopy confirms that strong hydrogen bonding hinders cation mobility. Application of the procedure to hybrid lead halide perovskites (X = Cl, Br, I, Am⁺ = CH₃NH₃⁺, CH(NH₂)₂⁺) shows that these compounds have significantly weaker hydrogen-bonding energies of 0.09 to 0.27 eV/cation (2-6 kcalmol^-1), correlating with lower order-disorder transition temperatures.

MgMnB2O5, Mg2/3Mn4/3B2O5, and Mg4/3Mn2/3B2O5 pyroborates have been prepared via a ceramic method. When charging MgMnB2O5 vs Li, all of the Mg2+ can be removed, and with subsequent cycles, 1.4 Li ions, corresponding to a capacity of 250 mAhg-1, can be reversibly intercalated. This is achieved at a C/25 rate with 99.6% Coulombic efficiency. Significant capacity is retained at high rates with 97 mAhg-1 at a rate of 2C. Continuous cycling at moderate rates gradually improves performance leading to insertion of 1.8 Li, 314 mAhg-1 with a specific energy of 802 Whkg-1, after 1000 cycles at C/5. Ex situ X-ray and neutron diffraction demonstrate the retention of the pyroborate structure on cycling vs Li and a small volume change (1%) between the fully lithiated and delithiated structures. Mg2/3Mn4/3B2O5 and Mg4/3Mn2/3B2O5 are also shown to reversibly intercalate Li at 17.8 and 188.6 mAhg-1, respectively, with Mn ions likely blocking Mg/Li transport in the Mg2/3Mn4/3B2O5 material. The electrochemical ion-exchange of polyanion materials with labile Mg ions could prove to be a route to high energy density Li-ion cathodes.

Li-substituted layered P2-Na0.80[Li0.12Ni 0.22Mn0.66]O2 is investigated as an advanced cathode material for Na-ion batteries. Both neutron diffraction and nuclear magnetic resonance (NMR) spectroscopy are used to elucidate the local structure, and they reveal that most of the Li ions are located in transition metal (TM) sites, preferably surrounded by Mn ions. To characterize structural changes occurring upon electrochemical cycling, in situ synchrotron X-ray diffraction is conducted. It is clearly demonstrated that no significant phase transformation is observed up to 4.4 V charge for this material, unlike Li-free P2-type Na cathodes. The presence of monovalent Li ions in the TM layers allows more Na ions to reside in the prismatic sites, stabilizing the overall charge balance of the compound. Consequently, more Na ions remain in the compound upon charge, the P2 structure is retained in the high voltage region, and the phase transformation is delayed. Ex situ NMR is conducted on samples at different states of charge/discharge to track Li-ion site occupation changes. Surprisingly, Li is found to be mobile, some Li ions migrate from the TM layer to the Na layer at high voltage, and yet this process is highly reversible. Novel design principles for Na cathode materials are proposed on the basis of an atomistic level understanding of the underlying electrochemical processes. These principles enable us to devise an optimized, high capacity, and structurally stable compound as a potential cathode material for high-energy Na-ion batteries. © 2014 American Chemical Society.