: reverse Monte Carlo for multiphase systems.

This work introduces a completely rewritten version of the program (version 7), big-box, reverse Monte Carlo modelling software for analysis of total scattering data. The major new feature of is the ability to refine multiple phases simultaneously, which is relevant for many current research areas such as energy materials, catalysis and engineering. Other new features include improved support for molecular potentials and rigid-body refinements, as well as multiple different data sets.

Melt-quenched glass formation of a family of metal-carboxylate frameworks.

Metal-organic framework (MOF) glasses are an emerging class of glasses which complement traditional inorganic, organic and metallic counterparts due to their hybrid nature. Although a few zeolitic imidazolate frameworks have been made into glasses, how to melt and quench the largest subclass of MOFs, metal carboxylate frameworks, into glasses remains challenging. Here, we develop a strategy by grafting the zwitterions on the carboxylate ligands and incorporating organic acids in the framework channels to enable the glass formation.

Electronic origin of negative thermal expansion in samarium hexaboride revealed by X-ray diffraction and total scattering.

Samarium hexaboride, SmB, is a negative thermal expansion (NTE) material whose structure is similar to other known NTE materials such as the family of Prussian blues. In the Prussian blues, NTE is due to a phonon mechanism, but we recently showed from DFT calculations that this is unlikely in SmB (Li , . 2023, , 10749).

Observation of the mixed magneto-optical Kerr effects using weak measurement.

In this paper, we use weak measurement to study the mixed magneto-optical Kerr effects (MOKEs) in a magnetic single layer of Co and in organic/Co bilayer films. The relationship between the amplified shift and the MOKE parameters is theoretically established and then experimentally observed as a function of both the magnetization intensity and the magnetization direction in magnetic thin films with an arbitrary magnetization. Furthermore, we experimentally observe a magnetic coupling at the organic/ferromagnetic interface.

Phonon mechanism for the negative thermal expansion of zirconium tungstate, ZrWO.

Negative thermal expansion (NTE) in ZrWO was investigated using a flexibility analysis of phonons. It was shown that no previously proposed mechanism adequately describes the atomic-scale origin of NTE in this material. Instead it was found that the NTE in ZrWO is driven, not by a single mechanism, but by wide bands of phonons that resemble vibrations of near-rigid WO units and Zr-O bonds at low frequency, with deformation of O-W-O and O-Zr-O bond angles steadily increasing with increasing NTE-phonon frequency.

The contribution of phonons to the thermal expansion of some simple cubic hexaboride structures: SmB, CaB, SrB and BaB.

We have performed first-principles calculations of the structure and lattice dynamics in the metal hexaborides SmB, CaB, SrB and BaB using Density Functional Theory in an attempt to understand the negative thermal expansion in the first of these materials. The focus is on the role of Rigid Unit Modes involving rotations of the B octahedra similar to the rotations of structural polyhedra connected by bonds in Zn(CN), Prussian Blue and Si(NCN). However, it was found that there is very low flexibility of the network of connected B octahedra, and the lattice dynamics do not support negative thermal expansion except possibly at very low temperature.

The rigid unit mode model: review of ideas and applications.

We review a set of ideas concerning the flexibility of network materials, broadly defined as structures in which atoms form small polyhedral units that are connected at corners. One clear example is represented by the family of silica polymorphs, with structures composed of corner-linked SiOtetrahedra. The rigid unit mode (RUM) is defined as any normal mode in which the structural polyhedra can translate and/or rotate without distortion, and since forces associated with changing the size and shape of the polyhedra are much stronger than those associated with rotations of two polyhedra around a shared vertex, the RUMs might be expected to have low frequencies compared to all other phonon modes.

Unique features of the structural phase transition in acetylene showing simultaneous characteristics of reconstructive, displacive and order-disorder.

We have studied the two phases of the molecular crystal acetylene, CH, using calculations of the lattice dynamics by Density Functional Theory methods. together with the use of classical molecular dynamics (MD) simulation methods. The two phases share the same simple face-centred cubic lattice arrangement of the molecular centres of mass, but with different molecular orientations.

Orientational disorder in sulfur hexafluoride: a neutron total scattering and reverse Monte Carlo study.

The orientational disorder in crystalline sulfur hexafluoride, SF, has been studied using a combination of neutron total scattering and the reverse Monte Carlo method. Analysis of the atomic configurations has shown the extent of the disorder through the evaluation of the S-F bond orientational distribution function, consistent with, but improving upon, the results of earlier neutron powder diffraction data. The correlations between orientations of neighbouring molecules have been studied through analysis of the distributions of F-F distances, showing that nearest-neighbour F-F close contacts are avoided, consistent with previous molecular dynamics simulation results.

Neutron powder-diffraction study of phase transitions in strontium-doped bismuth ferrite: 1. Variation with chemical composition.

We report results from a study of the crystal and magnetic structures of strontium-doped BiFeOusing neutron powder diffraction and the Rietveld method. Measurements were obtained over a wide range of temperatures from 300-800 K for compositions between 10%-16% replacement of bismuth by strontium. The results show a clear variation of the two main structural deformations-symmetry-breaking rotations of the FeOoctahedra and polar ionic displacements that give ferroelectricity-with chemical composition, but relatively little variation with temperature.

Neutron powder diffraction study of the phase transitions in deuterated methylammonium lead iodide.

We report the results of a neutron powder diffraction study of the phase transitions in deuterated methylammonium lead iodide, with a focus on the system of orientational distortions of the framework of PbIoctahedra. The results are analysed in terms of symmetry-adapted lattice strains and normal mode distortions. The higher-temperature cubic-tetragonal phase transition at 327 K is weakly discontinuous and nearly tricritical.

Origin of Ferroelectricity in Two Prototypical Hybrid Organic-Inorganic Perovskites.

Hybrid organic-inorganic perovskite (HOIP) ferroelectrics are attracting considerable interest because of their high performance, ease of synthesis, and lightweight. However, the intrinsic thermodynamic origins of their ferroelectric transitions remain insufficiently understood. Here, we identify the nature of the ferroelectric phase transitions in displacive [(CH)NH][Mn(N)] and order-disorder type [(CH)NH][Mn(HCOO)] via spatially resolved structural analysis and lattice dynamics calculations.

The ferroelastic phase transition in hydrogen cyanide studied by density functional theory.

We report calculations of the crystal structures and lattice dynamics of the tetragonal and orthorhombic phases of the molecular crystal hydrogen cyanide, HCN, using density functional theory methods. By treating negative pressure as a proxy for raising temperature we show that the ferroelastic phase transition involves softening of a transverse acoustic mode, and confirm that the phase transition is discontinuous. Analysis of the complete phonon spectrum shows that the acoustic modes are responsible both for the very large thermal expansion seen in HCN and also for the thermodynamic driving force for the phase transition.

Orientational order and phase transitions in deuterated methane: a neutron total scattering and reverse Monte Carlo study.

We report a study of the orientational order and phase transitions in crystalline deuterated methane, carried out using neutron total scattering and the reverse Monte Carlo method. The resultant atomic configurations are consistent with the average structures obtained from Rietveld refinement of the powder diffraction data, but additionally enable us to determine the C-D bond orientational distribution functions (ODF) for the disordered molecules in the high-temperature phase, and for both ordered and disordered molecules in the intermediate-temperature phase. We show that this approach gives more accurate information than can been obtained from fitting a bond ODF to diffraction data.

Analysis of the atomic structure of CdS magic-size clusters by X-ray absorption spectroscopy.

Magic-size clusters are ultra-small colloidal semiconductor systems that are intensively studied due to their monodisperse nature and sharp UV-vis absorption peak compared with regular quantum dots. However, the small size of such clusters (<2 nm), and the large surface-to-bulk ratio significantly limit characterisation techniques that can be utilised. Here we demonstrate how a combination of EXAFS and XANES analyses can be used to obtain information about sample stoichiometry and cluster symmetry.

Negative thermal expansion of cubic silicon dicarbodiimide, Si(NCN), studied bylattice dynamics.

We report ancalculation of crystal structure and lattice dynamics of cubic silicon dicarbodiimide, Si(NCN), using density functional theory methods. The calculations reveal a low-energy spectrum of rigid unit modes that are shown to be associated with negative thermal expansion. Comparisons are drawn with the closely-related materials Zn(CN)and the cubic-cristobalite phase of SiO.

Colossal Pressure-Induced Softening in Scandium Fluoride.

The counterintuitive phenomenon of pressure-induced softening in materials is likely to be caused by the same dynamical behavior that produces negative thermal expansion. Through a combination of molecular dynamics simulation on an idealized model and neutron diffraction at variable temperature and pressure, we show the existence of extraordinary and unprecedented pressure-induced softening in the negative thermal expansion material scandium fluoride ScF_{3}. The pressure derivative of the bulk modulus B, B^{'}=(∂B/∂P)_{P=0}, reaches values as low as -220±30 at 50 K, and is constant at -50 between 150 and 250 K.

Neutron scattering study of the orientational disorder and phase transitions in barium carbonate.

Orientational disorder of the molecularCO32-anions in BaCO, which occurs naturally as the mineral witherite, has been studied using a combination of neutron total scattering analysed by the reverse Monte Carlo method and molecular dynamics simulations. The primary focus is on the phase transition to the cubic phase, which assumes a rocksalt structure (Strukturbericht type B1) with highly disordered orientations consistent with the mismatch between the site (m3¯m) and molecular (3/) symmetries. Both experiment and simulation show a high degree of disorder, with the C-O bond orientation distribution never exceeding 25% variation from that of a completely uniform distribution, although there are differences between the two methods regarding the nature of these variations.

Adjustable uniaxial zero thermal expansion and zero linear compressibility in unique hybrid semiconductors: the role of the organic chain.

Zero thermal expansion (ZTE) and zero linear compressibility (ZLC) are unique and rare properties. Materials combining ZTE and ZLC will have promising prospects. A novel route is proposed in this work to design the coexistence of uniaxial-ZTE and ZLC based on layered hybrid semiconductors [ZnTe(L)0.

First-Principles Many-Body Nonadditive Polarization Energies from Monomer and Dimer Calculations Only: A Case Study on Water.

The many-body polarization energy is the major source of nonadditivity in strongly polar systems such as water. This nonadditivity is often considerable and must be included, if only in an average manner, to correctly describe the physical properties of the system. Models for the polarization energy are usually parametrized using experimental data, or theoretical estimates of the many-body effects.

X-ray total scattering study of magic-size clusters and quantum dots of cadmium sulphide.

Four types of magic-size CdS clusters and three different CdS quantum dots have been studied using the technique of X-ray total scattering and pair distribution function analysis. We found that the CdS quantum dots could be modelled as a mixed phase of atomic structures based on the two bulk crystalline phases, which is interpreted as representing the effects of random stacking of layers. However, the results for the magic-size clusters are significantly different.

Flexibility of network materials and the Rigid Unit Mode model: a personal perspective.

The Rigid Unit Mode model was initially developed to understand the origin of displacive phase transitions in network silicate structures. Here, we review the successes of the model, and consider how it might apply to a wider range of network structures. This article is part of the theme issue 'Mineralomimesis: natural and synthetic frameworks in science and technology'.

Hydrogen-bond-mediated structural variation of metal guanidinium formate hybrid perovskites under pressure.

The hybrid perovskites are coordination frameworks with the same topology as the inorganic perovskites, but with properties driven by different chemistry, including host-framework hydrogen bonding. Like the inorganic perovskites, these materials exhibit many different phases, including structures with potentially exploitable functionality. However, their phase transformations under pressure are more complex and less well understood.

Structural phase transitions in malononitrile, CH(CN): crystal structure of the δ phase by neutron powder diffraction, and ab initio calculations of the structures and phonons of the α and δ phases.

The crystal structure of the low-temperature [Formula: see text] phase of crystalline malononitrile, CH(CN) (stable phase below 260 K), has been determined using Rietveld refinement on neutron powder diffraction data. The [Formula: see text] phase has a slightly lower density than the other three low-pressure phases, and unlike those phases it has a polar structure. The transition from the [Formula: see text] to [Formula: see text] phase involves a major reconstruction of the structure, including establishing a network of hydrogen bonds.

Adsorption and migration of alkali metals (Li, Na, and K) on pristine and defective graphene surfaces.

In this paper, a computational study of Li, Na, and K adsorption and migration on pristine and defective graphene surfaces is conducted to gain insight into the metal storage and mobility in carbon-based anodes for alkali metal batteries. Atomic level studies of the metal adsorption and migration on the graphene surface can help address the challenges faced in the development of novel alkali metal battery technologies, as these systems act as convenient proxies of the crystalline carbon surface in carbon-based materials including graphite, hard carbons and graphene. The adsorption of Li and K ions on the pristine graphene surface is shown to be more energetically favourable than Na adsorption.