Chemical bonding in phase-change chalcogenides.

Almost all phase-change memory materials (PCM) contain chalcogen atoms, and their chemical bonds have been denoted both as 'electron-deficient' [sometimes referred to as 'metavalent'] and 'electron-rich' ['hypervalent', multicentre]. The latter involve lone-pair electrons. We have performed calculations that can discriminate unambiguously between these two classes of bond and have shown that PCM have electron-rich, 3c-4e ('hypervalent') bonds. Plots of charge transferred between (ET) and shared with (ES) neighbouring atoms cannot on their own distinguish between 'metavalent' and 'hypervalent' bonds, both of which involve single-electron bonds. PCM do not exhibit 'metavalent' bonding and are not electron-deficient; the bonding is electron-rich of the 'hypervalent' or multicentre type.

The gapless energy spectrum and spin-Peierls instability of 1D Heisenberg spin systems in polymeric complexes of transition metals and hypothetical carbon allotropes.

We investigate the spin-Peierls instability of some periodic 1D Heisenberg spin systems having a gapless energy spectrum at different values of coupling J between the unit cells. Using the density-matrix renormalization group method we numerically study the dependence of critical exponents p  of spin-Peierls transition of above spin systems on the value of J. In contrast to chain systems, we find significantly non-monotonous dependence p (J) for three-legs ladder system. In the limit of weak coupling J we derive effective spin s chain Hamiltonians describing the low-energy states of the system considered by means of perturbation theory. The value of site spin s coincides with the value of the ground-state spin of the isolated unit cell of the system considered. This means that at small J values all the systems with the singlet ground state and the same half-integer value of s should have a similar critical behavior which is in agreement with our numerical study. The presence of gapped excitations inside the unit cells at small values of J should give, for our spin systems, at least one intermediate plateau in field dependence of magnetization at low temperatures. The stability of this plateau against the increase of the values of J and temperature is studied using the quantum Monte-Carlo method.

Construction of a hybrid clamped cell for high-pressure neutron-diffraction experiments with a large diamond window.

A hybrid pressure cell was fabricated from commercially available copper-beryllium and custom-made Ni-Cr-Al Russian alloy, tailored for usage as a reaction vessel supplying a volume of about 400 mm3. In order to directly (in situ) monitor pressure and chemical reactions within the chamber, a large diamond window suitable for spectroscopic sample analysis was implemented. The performance of the hybrid cell was validated from high-pressure neutron-diffraction measurements on carbon dioxide.

The low-temperature heat capacity of the Sb2Te3-x Se x solid solution from experiment and theory.

The lattice dynamics of Sb2Te3-x Se x (x = 0, 0.6, 1.2, 1.8, 3) mixed crystals have been studied by a combination of low-temperature heat-capacity measurements between 2-300 K and first-principles calculations. The results from the experimental and theoretical investigations are in excellent agreement. While Sb2Se3 can be considered as a harmonic lattice oscillator in this temperature range, for the isostructural compounds Sb2Te3, Sb2Se0.6Te2.4, Sb2Se1.2Te1.8 and Sb2Se1.8Te1.2 (tetradymite structure type; R [Formula: see text] m) a small anharmonic contribution to the total heat capacity has to be taken into account at temperatures above 250 K. For the compounds which crystallize in the tetradymite structure type the experimental and theoretical data show unambiguously that the exchange of Te by Se leads to an increase of the bonding polarity and consequently to a hardening of the bonding which is reflected in an increase of the Debye temperatures with increasing Se contents. In addition, our studies clearly demonstrate that the mixed crystals in the stability field of the tetradymite structure type are characterized by a strong non-ideal mixing behavior.

Note: Efficient, low-cost cooling system for gloveboxes.

Cooling within gloveboxes is often restricted to expensive refrigerated bath circulators or small temperature differences. Here, we present a sturdy, inexpensive cooling system which matches various glovebox types and can be readily fabricated by a mechanical workshop in a few days. The system is suitable for cold plates of areas up to 150 cm2 and temperatures as low as -100 °C.

Low-temperature structure anomalies in CuNCN. Manifestations of RVB phase transitions?

We propose a new frustrated Heisenberg antiferromagnetic model with spatially anisotropic exchange parameters Jc, Ja, and Jac, extending along the c, a, and a ± c (c-a-ca model) lattice directions, and apply it to describe the fascinating physics of copper carbodiimide, CuNCN, assuming the resonating valence bond (RVB) type of its phases. This explains within a unified picture the intriguing absence of magnetic order in CuNCN. We further present a parameters-temperature phase diagram of the c-a-ca-RVB model in the high-temperature approximation. Eight different phases including Curie and Pauli paramagnets (respectively, in disordered and 1D- or Q1D-RVB phases) and (pseudo)gapped (quasi-Arrhenius) paramagnets (2D-RVB phases) are possible. By adding magnetostriction and elastic terms to the model, we derive possible structural manifestations of RVB phase transitions. Assuming a sequence of RVB phase transitions to occur in CuNCN with decreasing temperature, several anomalies observed in the temperature course of the lattice constants are explained.

Systematic study on the electronic structure and mechanical properties of X2BC (X = Mo, Ti, V, Zr, Nb, Hf, Ta and W).

In this work the electronic structure and mechanical properties of the phases X(2)BC with X =Ti, V, Zr, Nb, Mo, Hf, Ta, W (Mo(2)BC-prototype) were studied using ab initio calculations. As the valence electron concentration (VEC) per atom is increased by substitution of the transition metal X, the six very strong bonds between the transition metal and the carbon shift to lower energies relative to the Fermi level, thereby increasing the bulk modulus to values of up to 350 GPa, which corresponds to 93% of the value reported for c-BN. Systems with higher VEC appear to be ductile as inferred from both the more positive Cauchy pressure and the larger value of the bulk to shear modulus ratio (B/G). The more ductile behavior is a result of the more delocalized interatomic interactions due to larger orbital overlap in smaller unit cells. The calculated phase stabilities show an increasing trend as the VEC is decreased. This rather unusual combination of high stiffness and moderate ductility renders X(2)BC compounds with X = Ta, Mo and W as promising candidates for protection of cutting and forming tools.

Anosovite-type V3O5: a new binary oxide of vanadium.

The reaction of either V(2)F(6)·4H(2)O or a mixture of 60 wt % VF(2)·4H(2)O and 40 wt % VF(3)·3H(2)O with a water-saturated gaseous mixture of 15-20 vol % hydrogen in argon leads to the formation of a new polymorph of V(3)O(5) crystallizing in the orthorhombic anosovite-type structure. Quantum-chemical calculations show that the anosovite-type structure is about 15 kJ/mol less stable than the corresponding monoclinic Magnéli phase. In addition, there are no imaginary modes in the phonon density of states, supporting the classification of the anosovite-type phase as a metastable V(3)O(5) polymorph. Susceptibility measurements down to 3 K reveal no hint for magnetic ordering.

Electronic structure and thermodynamics of V2O3 polymorphs.

A metastable bixbyite-type polymorph of vanadium sesquioxide, V(2)O(3), has recently been synthesized, and it transforms to the corundum-type phase at temperatures around 550 °C. The possibility of a paramagnetic to canted antiferromagnetic or even spin-glass-like transition has been discussed. Quantum-chemical calculations on the density-functional theory level including explicit electronic correlation confirm the metastability as well as the semiconducting behavior of the material and predict that the bixbyite-type structure is about 0.1 eV less stable than the well-known corundum-type phase. Nonetheless, quasiharmonic phonon calculations manifest that bixbyite-type vanadium sesquioxide is a dynamically stable compound. Other possible V(2)O(3) polymorphs are shown to be even less suitable candidates for the composition V(2)O(3).

Unconventional magnetism in a nitrogen-containing analog of cupric oxide.

We have investigated the magnetic properties of CuNCN, the first nitrogen-based analog of cupric oxide CuO. Our muon-spin relaxation, nuclear magnetic resonance, and electron-spin resonance studies reveal that classical magnetic ordering is absent down to the lowest temperatures. However, a large enhancement of spin correlations and an unexpected inhomogeneous magnetism have been observed below 80 K. We attribute this to a peculiar fragility of the electronic state against weak perturbations due to geometrical frustration, which selects between competing spin-liquid and more conventional frozen states.

Bixbyite-type V2O3--a metastable polymorph of vanadium sesquioxide.

A metastable polymorph of vanadium sesquioxide was prepared by the reaction of vanadium trifluoride with a water-saturated gaseous mixture of 10 vol % hydrogen in argon. The new polymorph crystallizes in the bixbyite-type structure. At temperatures around 823 K a transformation to the well-known corundum-type phase is observed. Quantum-chemical calculations show that the bixbyite-type structure is about 9 kJ/mol less stable than the known corundum-based one. This result, in combination with the absence of imaginary modes in the phonon density of states, supports the classification of the bixbyite-type phase as a metastable V(2)O(3) polymorph. At ~50 K a paramagnetic to canted antiferromagnetic transition is detected.

Hydrogen-bond networks in finite ice nanotubes.

An exhaustive analysis of all H-bond networks for finite elements of ice nanotubes formed by up to 32 water molecules (3,660,732 configurations in total) is performed. The results constitute a unique database and demonstrate the H-bond network formation and changes with the growth of the ice nanotube. The statistical analysis shows that H-bonds can be classified according to their structural positions, and there are remarkable dependencies of the cooperativity energy and bond lengths on the system's morphology. The study of low-energy configurations supports the conclusion about the ferroelectric order in ice nanotubes with odd numbers of water molecules in the ring.

Multipole model for the electron group functions method.

Electron groups provide a natural way to introduce local concepts into quantum chemistry, and the wave functions based on the group products can be considered as a framework for constructing efficient computational methods in terms of "observable" parts of molecular systems. The elements of the group wave functions (electronic structure variables) can be optimized by requiring the number of operations proportional to the size of the molecule. This directly leads to computational methods linearly scaling for large molecular systems. In the present work we consider a particular case of such a wave function implemented for the semiempirical NDDO Hamiltonian. The electron groups are expressed in terms of optimized atomic (hybrid) orbitals with chemical bonds described by geminals and the delocalized groups described by Slater determinants (with or without spin restriction). This scheme is very fast by itself but its speed is considerably limited by the computations of the interatomic Coulomb interactions. Here we develop a consistent method based on group functions which uses the multipole scheme for interatomic interactions. The explicit usage of the atomic multipoles makes the method extremely fast, although the numerical efficiency is largely achieved due to the local character of the electron groups involved. We discuss numerical characteristics of the new method as well as its possible parametrization. We apply this method to study dodecahedral water clusters with hydrogen fluoride substitution and base the analysis on the exhaustive calculation of all symmetry-independent hydrogen-bond networks.

Electron group functions for the analysis of the electronic structures of molecules.

The electronic structure of a vast majority of molecular systems can be understood in terms of electron groups and their wave functions. They serve as a natural basis for bringing intuitive chemical and physical concepts into quantum chemical calculations. This article considers the general electron group functions formalism as well as its simple geminal version. We try to characterize the wave function with the group structure and its capabilities in actual calculations. For this purpose we implement a variational method based on the wave function in the form of an antisymmetrized product of strongly orthogonal group functions and perform a series of electronic structure calculations for small molecules and model systems. The most important point studied is the relation between the choice of electron groups and the results obtained. We consider energetic characteristics as well as optimal geometry parameters. In view of practical importance, the structure of variationally optimized local one-electron states is considered in detail as well as intuitive characteristics of chemical bonds.

The Orbital Origins of Magnetism: From Atoms to Molecules to Ferromagnetic Alloys.

A chemical view of spin magnetic phenomena in finite (atoms and molecules) and infinite (transition metals and their alloys) systems using the concepts of bonding and electronic shielding is presented. The concept is intended to serve as a semiquantitative signpost for the synthesis of new ferromagnets. After a concise overview of the historic development of related theories developed within the physics community, the consequences of spin-spin coupling (made manifest in the exchange or Fermi hole) in atoms and molecules are explored. Upon moving to a paramagnetic state, the majority/minority spin species become more/less tightly bound to the nucleus, resulting in differences in the energies and spatial extents of the two sets of spin orbitals. By extrapolating well-known arguments from ligand-field theory, the paucity of ferromagnetic transition metals arises from quenching the paramagnetism of the free atoms due to strong interatomic interactions in the solid state. Critical valence electron concentrations in Fe, Co, and Ni, however, result in local electronic instabilities due to the population of antibonding states at the Fermi level varepsilon(F). Removal of these antibonding states from the vicinity of varepsilon(F) is the origin of ferromagnetism; in the pure metals this results in strengthening the chemical bonds. In the 4d and 5d transition metals, the valence d orbitals are too well shielded from the nucleus, so a transition to a ferromagnetic state does not result in sufficiently large changes to occur. Thus, the exceptional occurence of ferromagnetism only in the first transition series appears to parallel the special main-group chemistry of the first long period. A connection between ferromagnetism in the transition metals and Pearson's absolute hardness eta is easily established and shows that ferromagnetism appears only when eta<0.2 eV in the nonmagnetic calculation. As expected from the principle of maximum hardness, Fe, Co, and Ni all become harder upon moving to the more stable ferromagnetic state. Magnetism in intermetallic alloys follows the same path. Whether or not an alloy contains ferromagnetic elements, the presence of antibonding states at varepsilon(F) serves as a "fingerprint" to indicate a ferromagnetic instability. The differences in the sizes of the local magnetic moments on the constituent atoms of a ferromagnetic alloy can be understood in terms of the relative contributions to the density of states at varepsilon(F) in the nonmagnetic calculations. Appropriately parameterized, nonmagnetic, semi-empirical calculations can also be used to expose the ferromagnetic instability in elements and alloys. These techniques, which have become relatively commonplace, can be used to guide the synthetic chemist in search of new ferromagnetic materials.