Investigating materials with disordered structures using total neutron scattering

The structures of a variety of disordered materials were determined using the technique of total neutron scattering. The synthesis of various polymorphs of Ga2O3 and related materials was investigated and the structures of the hitherto uncharacterised polymorphs were examined in detail. The structure of y-Ga2O3 was found to be a cubic defect spinel with four partially occupied Ga sites, however, the octahedral Ga coordination environments were found to be distorted from the average cubic structure. The cation distribution in y-Ga2O3 was found to depend on particle size and synthesis method. Examination of the structure of E-Ga2O3 revealed that it is analogous to a disordered, hexagonal form of E-Fe2O3. The poorly crystalline product of the thermal decomposition of Ga(NO3)3.9H2O was found to be a nanocrystalline modification of E-Ga2O3, rather than a distinct phase with the bixbyite structure, as had been previously reported. The structure of a novel gallium oxyhydroxide, Ga5O7(OH), was determined to be analogous to tohdite, Al5O7(OH), and in its thermal decomposition pathway was revealed a new Ga2O3 polymorph: orthorhombic K-Ga2O3. A solvothermal synthetic route to spinel structured ternary gallium oxides, of general formula MxGa3-xO4-y, was developed. The structures of the materials where M = Zn or Ni were found to be consistent with those previously published. The materials where M = Co or Fe possess novel, oxygen-deficient compositions and exhibit interesting magnetic behaviour. A series of cerium bismuth oxides of formula Ce1-xBixO2-1/2x were found to adopt the cubic fluorite structure with significant local distortion due to the preference of Bi3+ for an asymmetric coordination environment. A sodium cerium titanate pyrochlore was also structurally characterised and it was determined that, due to the presence of three different cations on the A site, the local structure required a model with reduced symmetry. In situ neutron scattering experiments were carried out on amorphous zeolite precursor gels in the presence of the reaction liquid. These experiments revealed structural features unique to the gel, and proved that the gel undergoes irreversible structural changes on drying. Preliminary analysis of the gel structure indicated that the Na+ cations play an important role in the development of the ordered zeolitic framework, and revealed no strong evidence for the existence of discrete structural building units in the gel

Structural disorder in (Bi,M)2(Fe,Mn,Bi)2O6+x (M = Na or K) pyrochlores seen from reverse Monte Carlo analysis of neutron total scattering

The average structures of the polycrystalline pyrochlores (Na0.60Bi1.40)(Fe1.06Mn0.17Bi0.77)O6.87 and (K0.24Bi1.51)(Fe1.07Mn0.15Bi0.78)O6.86 can be refined through Rietveld refinement against Bragg scattering data using cubic space group Fd3 ̅m, with off-centred 96h and 32e positions describing the A2Oʹ network. Investigation of their local structures through neutron total scattering confirms the extent of disorder within these materials, and furthermore shows significant deviation from the average structure, which is not accounted for through analysis of Bragg data alone. Reverse Monte Carlo (RMC) analysis with a 6 × 6 × 6 supercell was used to model accurately this local disorder, revealing ellipsoidal distributions for A-site potassium, distinctly different to the hollow torus-shaped distributions for the sodium and bismuth cations. It is shown through bond valence sum analysis that whilst these atomic displacements allow for the steric preferences of Bi3+, they are also necessary to satisfy the valence of both the bismuth and the alkali metals on the A sites. Analysis of the final RMC configuration showed the BO6 octahedra for the separate B site metals to be more regular (O–B–O ≈ 90°) than those in the Rietveld model (O–B–O ≈ 85/95°) which describes an average of the three different environments

Structure–property insights into nanostructured electrodes for Li-ion batteries from local structural and diffusional probes

Microwave heating presents a faster, lower energy synthetic methodology for the realization of functional materials. Here, we demonstrate for the first time that employing this method also leads to a decrease in the occurrence of defects in olivine structured LiFe1−xMnxPO4. For example, the presence of antisite defects in this structure precludes Li+ diffusion along the b-axis leading to a significant decrease in reversible capacities. Total scattering measurements, in combination with Li+ diffusion studies using muon spin relaxation (μ+SR) spectroscopy, reveal that this synthetic method generates fewer defects in the nanostructures compared to traditional solvothermal routes. Our interest in developing these routes to mixed-metal phosphate LiFe1−xMnxPO4 olivines is due to the higher Mn2+/3+ redox potential in comparison to the Fe2+/3+ pair. Here, single-phase LiFe1−xMnxPO4 (x = 0, 0.25, 0.5, 0.75 and 1) olivines have been prepared following a microwave-assisted approach which allows for up to 4 times faster reaction times compared to traditional solvothermal methods. Interestingly, the resulting particle morphology is dependent on the Mn content. We also examine their electrochemical performance as active electrodes in Li-ion batteries. These results present microwave routes as highly attractive for reproducible, gram-scale syntheses of high quality nanostructured electrodes which display close to theoretical capacity for the full iron phase

Orbital Dimer Model for Spin-Glass State in Y2_2Mo2_2O7_7

The formation of a spin glass usually requires both structural disorder and frustrated magnetic interactions. Consequently, the origin of spin-glass behaviour in Y$_2$Mo$_2$O$_7$ $-$ in which magnetic Mo$^{4+}$ ions occupy a frustrated pyrochlore lattice with minimal compositional disorder $-$ has been a longstanding question. Here, we use neutron and X-ray pair-distribution function (PDF) analysis to develop a disorder model that resolves apparent incompatibilities between previously-reported PDF, EXAFS and NMR studies and provides a new and physical mechanism for spin-glass formation. We show that Mo$^{4+}$ ions displace according to a local "2-in/2-out" rule on each Mo$_4$ tetrahedron, driven by orbital dimerisation of Jahn-Teller active Mo$^{4+}$ ions. Long-range orbital order is prevented by the macroscopic degeneracy of dimer coverings permitted by the pyrochlore lattice. Cooperative O$^{2-}$ displacements yield a distribution of Mo$-$O$-$Mo angles, which in turn introduces disorder into magnetic interactions. Our study demonstrates experimentally how frustration of atomic displacements can assume the role of compositional disorder in driving a spin-glass transition.Comment: 6 pages, 3 figure

The upgraded Polaris powder diffractometer at the ISIS neutron source

This paper describes the design and operation of the Polaris time-of-flight powder neutron diffractometer at the ISIS pulsed spallation neutron source, Rutherford Appleton Laboratory, UK. Following a major upgrade to the diffractometer in 2010-2011, its detector provision now comprises five large ZnS scintillator-based banks, covering an angular range of 6\ub0 ≤ 2θ ≤ 168\ub0, with only minimal gaps between each bank. These detectors have a substantially increased solid angle coverage (ω ∼5.67 sr) compared to the previous instrument (ω ∼0.82 sr), resulting in increases in count rate of between 2 7 and 10 7, depending on 2θ angle. The benefits arising from the high count rates achieved are illustrated using selected examples of experiments studying small sample volumes and performing rapid, time-resolved investigations. In addition, the enhanced capabilities of the diffractometer in the areas of in situ studies (which are facilitated by the installation of a novel design of radial collimator around the sample position and by a complementary programme of advanced sample environment developments) and in total scattering studies (to probe the nature of short-range atomic correlations within disordered crystalline solids) are demonstrated

Study of the B-site ion behaviour in the multiferroic perovskite bismuth iron chromium oxide

A simple, near-ambient pressure solid-state method was developed to nominally synthesize BiFe0.5Cr0.5O3. The procedure allowed the gram-scale production of multiferroic samples with appreciable purity and large amounts of Cr incorporation that were suitable for systematic structural investigation by neutron, X-ray, and electron diffraction in tandem with physical characterization of magnetic and ferroelectric properties. The rhombohedrally distorted perovskite phase was assigned to the space group R3c by way of X-ray and neutron powder diffraction analysis. Through a combination of magnetometry and muon spin relaxation, it is evident that there is magnetic ordering in the BFCO phase consistent with G-type antiferromagnetism and a TN 400 K. There is no clear evidence for chemical ordering of Fe and Cr in the B-site of the perovskite structure and this result is rationalized by density functional theory and bond valence simulations that show a lowered energy associated with a B-site disordered structure. We believe that our contribution of a new, low-complexity method for the synthesis of BFO type samples, and dialogue about realising certain types of ordering in oxide perovskite systems, will assist in the further development of multiferroics for next-generation devices. Published by AIP Publishing. https://doi.org/10.1063/1.5020305B.R.M., J.L., A.B., D.L.C., T.L., R.L.W., N.N., and Y.L. acknowledge the support of the Australian Research Council (ARC) in the form of Discovery Projects (No. DP160104780). A.B., D.L.C., N.N., D.Y. and authors thank the Australian Nuclear Science and Technology Organisation (ANSTO) for facilities and financial support and also thank the Echidna instrument scientists for their expertise

Local structure and order-disorder transitions in "empty" ferroelectric tetragonal tungsten bronzes

JAM would like to acknowledge the School of Chemistry, University of St Andrews for the allocation of a PhD studentship through the EPSRC doctoral training grant (EP/K503162/1). AR would like to acknowledge support through the Strategic Grant POSDRU/159/1.5/S/133255, Project ID 133255 (2014), co-financed by the European Social Fund within the Sectorial Operational Program Human Resources Development 2007–2013 and also the University of Craiova and University of Cambridge for the mobility grant “Resonant ultrasound spectroscopy. (RUS) characterization of dielectric and ferroelectric tetragonal tungsten bronzes”. The work carried out at the University of St Andrews and University of Cambridge is part of an EPSRC- funded collaboration (EP/P02453X/1 and EP/P024904/1).The ‘empty’ tetragonal tungsten bronze Ba4La0.67 1.33Nb10O30 displays both relaxor-like and normal dielectric anomalies as a function of temperature; the former is associated with loss of ferroelectricity and was proposed to originate from anion disordering [Chem. Mater., 2016, 28 , 4616-4627]. Here we present total neutron scattering and pair distribution function (PDF) analysis which shows an increase in the distribution of oxygen-oxygen distances at the relaxor transition and which supports the proposed anion disordering mechanism. The disordering process can be destabilised by reducing the average A-cation size (i.e. Nd-doping: Ba4(La1-xNdx)0.67Nb10O30); this introduces a more strongly propagating tilt system in line with the previously reported crystal-chemical framework model [Chem. Mater., 2015, 27 , 3250-3261]. Mechanical loss data obtained using resonant ultrasound spectroscopy also indicate destabilisation of the disordering process with increasing Nd-substitution.PostprintPeer reviewe

Redox Chemistry and the Role of Trapped Molecular O₂in Li-Rich Disordered Rocksalt Oxyfluoride Cathodes

In the search for high energy density cathodes for next-generation lithium-ion batteries, the disordered rocksalt oxyfluorides are receiving significant attention due to their high capacity and lower voltage hysteresis compared with ordered Li-rich layered compounds. However, a deep understanding of these phenomena and their redox chemistry remains incomplete. Using the archetypal oxyfluoride, Li2MnO2F, we show that the oxygen redox process in such materials involves the formation of molecular O2 trapped in the bulk structure of the charged cathode, which is reduced on discharge. The molecular O2 is trapped rigidly within vacancy clusters and exhibits minimal mobility unlike free gaseous O2, making it more characteristic of a solid-like environment. The Mn redox process occurs between octahedral Mn3+ and Mn4+ with no evidence of tetrahedral Mn5+ or Mn7+. We furthermore derive the relationship between local coordination environment and redox potential; this gives rise to the observed overlap in Mn and O redox couples and reveals that the onset potential of oxide ion oxidation is determined by the degree of ionicity around oxygen, which extends models based on linear Li-O-Li configurations. This study advances our fundamental understanding of redox mechanisms in disordered rocksalt oxyfluorides, highlighting their promise as high capacity cathodes

Redox Chemistry and the Role of Trapped Molecular O₂in Li-Rich Disordered Rocksalt Oxyfluoride Cathodes

In the search for high energy density cathodes for next-generation lithium-ion batteries, the disordered rocksalt oxyfluorides are receiving significant attention due to their high capacity and lower voltage hysteresis compared with ordered Li-rich layered compounds. However, a deep understanding of these phenomena and their redox chemistry remains incomplete. Using the archetypal oxyfluoride, Li2MnO2F, we show that the oxygen redox process in such materials involves the formation of molecular O2 trapped in the bulk structure of the charged cathode, which is reduced on discharge. The molecular O2 is trapped rigidly within vacancy clusters and exhibits minimal mobility unlike free gaseous O2, making it more characteristic of a solid-like environment. The Mn redox process occurs between octahedral Mn3+ and Mn4+ with no evidence of tetrahedral Mn5+ or Mn7+. We furthermore derive the relationship between local coordination environment and redox potential; this gives rise to the observed overlap in Mn and O redox couples and reveals that the onset potential of oxide ion oxidation is determined by the degree of ionicity around oxygen, which extends models based on linear Li-O-Li configurations. This study advances our fundamental understanding of redox mechanisms in disordered rocksalt oxyfluorides, highlighting their promise as high capacity cathodes.</p

Structure, Spin Correlations, and Magnetism of the S = 1/2 Square-Lattice Antiferromagnet Sr2CuTe1-xWxO6 (0 ≤ x ≤ 1)

Quantum spin liquids are highly entangled magnetic states with exotic properties. The S = 1/2 square-lattice Heisenberg model is one of the foundational models in frustrated magnetism with a predicted, but never observed, quantum spin liquid state. Isostructural double perovskites Sr2CuTeO6 and Sr2CuWO6 are physical realizations of this model but have distinctly different types of magnetic order and interactions due to a d10/d0 effect. Long-range magnetic order is suppressed in the solid solution Sr2CuTe1-xWxO6 in a wide region of x = 0.05-0.6, where the ground state has been proposed to be a disorder-induced spin liquid. Here, we present a comprehensive neutron scattering study of this system. We show using polarized neutron scattering that the spin liquid-like x = 0.2 and x = 0.5 samples have distinctly different local spin correlations, which suggests that they have different ground states. Low-temperature neutron diffraction measurements of the magnetically ordered W-rich samples reveal magnetic phase separation, which suggests that the previously ignored interlayer coupling between the square planes plays a role in the suppression of magnetic order at x ≈ 0.6. These results highlight the complex magnetism of Sr2CuTe1-xWxO6 and hint at a new quantum critical point between 0.2 &lt; x &lt; 0.4.</p