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Peter Schwerdtfeger

Publications and source records attributed to Peter Schwerdtfeger.

At least 19 recordsLinked to original sources

Lattice Instabilities Along the Transformation from Hexagonal to Cuboidal Structures in Hard- and Soft-Sphere Models

The diffusionless Burgers-Bain phase transition from a hcp arrangement to a cuboidal lattice (fcc and bcc) is analysed in great detail for Lennard-Jones solids. From the lattice vectors of an underlying bi-lattice smoothly connecting these phases, we are able to express the corresponding lattice sums for inverse power potentials in terms of fast converging Bessel function expansions resulting in an efficient evaluation to computer accuracy for cohesive energies. From the kissing hard-sphere limit we derive exact analytical expressions for the lattice parameters varying along the minimum energy path of the phase transition. This simple model suggests that for the Burgers-Bain transformation of a LJ solid requires a minimum of four lattice parameters, $(a,α,β,γ=c/a)$, describing the change in the base lattice lengths $a$ and $c$, the shear force acting on the hexagonal base plane ($α$), the sliding force of the middle layer of the original hexagonal packing arrangement($β$), and the cuboidal transformation ($γ=c/a$). This choice results in a two-step process: hcp$\to$fcc$\to$bcc. However, a further extension of the parameter space including an additional slide parameter for the middle layer, one suddenly observes a distinct symmetry-breaking effect along the hcp$\rightarrow$fcc transition path with a bifurcation point appearing joining the original Burgers with the Bain path of the bcc$\rightarrow$fcc cuboidal transition. Furthermore, for soft LJ potentials the bcc phase appears as a local minimum along the Burgers hcp$\rightarrow$fcc path with two transition states to either the hcp or fcc phase. The underlying topology of the Burgers-Bain phase transition also incorporates the rhombohedral distortion of the bcc phase, which is analyzed in detail.

cond-mat.mtrl-sci

Exact lattice summations for Lennard-Jones potentials coupled to a three-body Axilrod-Teller-Muto term applied to cuboidal phase transitions

This work provides a rigorous analysis of Bain-type cuboidal lattice transformations, which connect the face-centered cubic (fcc), mean-centered cubic (mcc), body-centered cubic (bcc) and axially centered cubic (acc) lattices. Our study incorporates a general $(n,m)$ Lennard-Jones two-body potential and a long-range repulsive Axilrod-Teller-Muto (ATM) three-body potential. The two-body lattice sums and their meromorphic continuations are evaluated to full precision using super-exponentially convergent series expansions. Furthermore, we introduce a novel approach to computing three-body lattice sums by converting the multi-dimensional sum into an integral involving products of Epstein zeta functions. This enables us to evaluate three-body lattice sums and their meromorphic continuations to machine precision within minutes on a standard laptop. Using our computational framework, we analyze the stability of cuboidal lattice phases relative to the close-packed fcc structure along a Bain transformation path for varying ATM coupling strengths. We analytically demonstrate that the ATM cohesive energy exhibits an extremum at the bcc phase and show numerically that it corresponds to a minimum for repulsive three-body forces along the Bain path. Our results indicate that strong repulsive three-body interactions can destabilize the fcc phase and render bcc energetically favorable for soft LJ potentials. However, even in this scenario, the bcc phase remains susceptible to further cuboidal distortions. These results suggest that the stability of the bcc phase is, besides vibrational, temperature, and pressure effects, strongly influenced by higher than two-body forces. Because of the wrong short-range behavior of the triple-dipole ATM model the LJ potential is limited to exponents $n>9$ for the repulsive wall, otherwise one observes distortion into a set of linear chains collapsing to the origin.

cond-mat.mtrl-sci

A Minimum Property for Cuboidal Lattice Sums

We analyse a family of lattices considered by Conway and Sloane and show that the corresponding Epstein zeta function attains a local minimum for the body-centred cubic lattice.

math.NT

Exploring the mechanism of phase transitions between the hexagonal close-packed and the cuboidal structures

By introducing appropriate lattice parameters for a bi-lattice smoothly connecting the hexagonal close-packed (hcp) with the cuboidal structures, namely the body-centered (bcc) and the face centered cubic (fcc) lattices, we were able to map out the minimum energy path for a Burgers-Bain type of phase transition. We demonstrate that for three different models applied, i.e. the kissing hard-sphere model, the Lennard-Jones potential, and density functional theory for metallic lithium, the direct transition path is always from hcp to fcc with a separate path leading from fcc to bcc. This solves, at least for the models considered here, a long-standing controversy of whether or not fcc acts as an intermediate phase in martensitic type of phase transitions.

cond-mat.mtrl-sci

Quantum electrodynamic corrections for molecules: Vacuum polarisation and electron self energy in a two-component relativistic framework

Vacuum polarisation (VP) and electron self energy (SE) are implemented and evaluated as quantum electrodynamic (QED) corrections in a (quasi-relativistic) two-component zeroth order regular approximation (ZORA) framework. For VP, the Uehling potential is considered, and for SE, the effective potentials proposed by Flambaum and Ginges as well as the one proposed by Pyykkö and Zhao. QED contributions to ionisation energies of various atoms and group 2 monofluorides, group 1 and 11 valence orbital energies, $^2\mathrm{P}_{1/2} \leftarrow {}^{2}\mathrm{S}_{1/2}$ and $^{2}\mathrm{P}_{3/2} \leftarrow {}^{2}\mathrm{S}_{1/2}$ transition energies of Li-, Na-, and Cu-like ions of nuclear charge $Z$ = 10, 20, ..., 90 as well as $Π_{1/2}\leftarrow Σ_{1/2}$ and $Π_{3/2}\leftarrowΣ_{1/2}$ transition energies of BaF and RaF are presented. Furthermore, perturbative and self-consistent treatments of QED corrections are compared for Kohn--Sham orbital energies of gold. It is demonstrated, that QED corrections can be obtained in a two-component ZORA framework efficiently and in excellent agreement with corresponding four-component results.

physics.chem-ph

Large Vibrationally Induced Parity Violation Effects in CHDBrI$^+$ $-$ A Promising Candidate for Future Experiments

The isotopically chiral molecular ion CHDBrI$^+$ is identified as an exceptionally promising candidate for the detection of parity violation in vibrational transitions. The largest predicted parity-violating frequency shift reaches 1.8 Hz for the hydrogen wagging mode which has a sub-Hz natural line width and its vibrational frequency auspiciously lies in the available laser range. In stark contrast to this result, the parent neutral molecule is two orders of magnitude less sensitive to parity violation. The origin of this effect is analyzed and explained. Precision vibrational spectroscopy of CHDBrI$^+$ is feasible as it is amenable to preparation at internally low temperatures and resistant to predissociation, promoting long interrogation times (Landau et al.). The intersection of these properties in this molecular ion places the first observation of parity violation in chiral molecules within reach.

physics.chem-ph

Solving a problem with a single parameter: A smooth bcc to fcc phase transition for metallic lithium

Density functional calculations for metallic lithium along a cuboidal bcc-to-fcc transformation path demonstrate that the bcc phase is quasi-degenerate with the fcc phase with a very small activation barrier of 0.1~kJ/mol, but becomes the dominant phase at higher temperatures in accordance with Landau theory. This resolves the long-standing controversy about the two phases for lithium.

cond-mat.mtrl-sci

Towards detection of the molecular parity violation in chiral Ru(acac)$_3$ and Os(acac)$_3$

We present a theory-experiment investigation of the helically chiral compounds Ru(acac)$_3$ and Os(acac)$_3$ as candidates for the next-generation experiments for detection of molecular parity violation (PV) in vibrational spectra. We used state-of-the-art relativistic calculations to identify optimal vibrational modes with expected PV effects exceeding by up to two orders of magnitude the projected instrumental sensitivity of the experiment under construction at the Laboratoire de Physique des Lasers in Paris. High-resolution measurements of the vibrational spectrum of Ru(acac)$_3$ carried out as the first steps towards the planned experiment are presented.

physics.chem-ph

The Madelung Constant in $N$ Dimensions

We introduce two convergent series expansions (direct and recursive) in terms of Bessel functions and representations of sums $r_N(m)$ of squares for $N$-dimensional Madelung constants, $M_N(s)$, where $s$ is the exponent of the Madelung series (usually chosen as $s=1/2$). The functional behavior including analytical continuation, and the convergence of the Bessel function expansion is discussed in detail. Recursive definitions are used to evaluate $r_N(m)$. Values for $M_N(s)$ for $s=\tfrac{1}{2}, \tfrac{3}{2}, 3$ and 6 for dimension up to $N=20$ and for $M_N(1/2)$ up to $N=100$ are presented. Zucker's original analysis on $N$-dimensional Madelung constants for even dimensions up to $N=8$ and their possible continuation into higher dimensions is briefly analyzed.

math-ph

Instability of the Body-Centered Cubic Lattice within the Sticky Hard Sphere and Lennard-Jones Model obtained from Exact Lattice Summations

A smooth path of rearrangement from the body-centered cubic (bcc) to the face-centered cubic (fcc) lattice is obtained by introducing a single parameter to cuboidal lattice vectors. As a result, we obtain analytical expressions in terms of lattice sums for the cohesive energy. This is described by a Lennard-Jones (LJ) interaction potential and the sticky hard sphere (SHS) model with an $r^{-n}$ long-range attractive term. These lattice sums are evaluated to computer precision by expansions in terms of a fast converging series of Bessel functions. Applying the whole range of lattice parameters for the SHS and LJ potentials demonstrates that the bcc phase is unstable (or at best metastable) toward distortion into the fcc phase. Even if more accurate potentials are used, such as the extended LJ potential for argon or chromium, the bcc phase remains unstable. This strongly indicates that the appearance of a low temperature bcc phase for several elements in the periodic table is due to higher than two-body forces in atomic interactions.

cond-mat.mtrl-sci

The Cuboidal Lattices and their Lattice Sums

Lattice sums of cuboidal lattices, which connect the face-centered with the mean-centered and the body-centered cubic lattices through parameter dependent lattice vectors, are evaluated by decomposing them into two separate lattice sums related to a scaled cubic lattice and a scaled Madelung constant. Using theta functions we were able to derive fast converging series in terms of Bessel functions. Analytical continuations of these lattice sums are discussed in detail.

math-ph

The Lennard Jones Potential Revisited -- Analytical Expressions for Vibrational Effects in Cubic and Hexagonal Close-Packed Lattices

Analytical formulae are derived for the zero-point vibrational energy and anharmonicity corrections of the cohesive energy and the mode Grüneisen parameter within the Einstein model for the cubic lattices (sc, bcc and fcc) and for the hexagonal close-packed structure. This extends the work done by Lennard Jones and Ingham in 1924, Corner in 1939 and Wallace in 1965. The formulae are based on the description of two-body energy contributions by an inverse power expansion (extended Lennard-Jones potential). These make use of three-dimensional lattice sums, which can be transformed to fast converging series and accurately determined by various expansion techniques. We apply these new lattice sum expressions to the rare gas solids and discuss associated critical points. The derived formulae give qualitative but nevertheless deep insight into vibrational effects in solids from the lightest (helium) to the heaviest rare gas element (oganesson), both presenting special cases because of strong quantum effects for the former and strong relativistic effects for the latter.

cond-mat.mtrl-sci

Electron and Nucleon Localization Functions of Oganesson: Approaching the Thomas-Fermi Limit

Fermion localization functions are used to discuss electronic and nucleonic shell structure effects in the superheavy element oganesson, the heaviest element discovered to date. Spin-orbit splitting in the $7p$ electronic shell becomes so large ($\sim$ 10 eV) that Og is expected to show uniform-gas-like behavior in the valence region with a rather large dipole polarizability compared to the lighter rare gas elements. The nucleon localization in Og is also predicted to undergo a transition to the Thomas-Fermi gas behavior in the valence region. This effect, particularly strong for neutrons, is due to the high density of single-particle orbitals.

nucl-th

Material Size Dependence on Fundamental Constants

Precise experimental setups for detection of variation of fundamental constants, scalar dark matter, or gravitational waves, such as laser interferometers, optical cavities and resonant-mass detectors, are directly linked to measuring changes in material size. Here we present calculated and experiment-derived estimates for both $α$- and $μ$-dependence of lattice constants and bond lengths of selected solid-state materials and diatomic molecules that are needed for interpretation of such experiments.

physics.chem-ph

The Static Dipole Polarizability of Palladium from Relativistic Coupled Cluster Theory

Nonrelativistic and relativistic coupled-cluster calculations extrapolated to the complete basis set limit including excitations up to the quintuple level (CCSDTQP) were carried out to accurately determine the static electric dipole polarizability of the closed-shell palladium atom. The resulting value of $α$ = 26.14(10) a.u. implies that palladium has the smallest dipole polarizability of all known elemental metal atoms due to its unique 4d$^{10}$5s$^0$ configuration. Relativistic effects are found to be already sizeable ($Δ_Rα$= +1.86~a.u.) compared to electron correlation ($Δ_Cα$= +5.06~a.u.), and need to be included for the accurate determination of the dipole polarizability. We also report a value of the second hyperpolarizability to be $γ\approx$ 40,000~a.u., but here the coupled-cluster contributions are not yet converged out with respect to higher than quintuple excitations.

physics.atom-ph

The nuclear anapole moment interaction in BaF from relativistic coupled cluster theory

We present high accuracy relativistic coupled cluster calculations of the P-odd interaction coefficient $W_A$ describing the nuclear anapole moment effect on the molecular electronic structure. The molecule under study, BaF, is considered a promising candidate for the measurement of the nuclear anapole moment, and the preparation for the experiment is now underway [Altunas et al., Phys. Rev. Lett. 120, 142501 (2018)]. Influence of various computational parameters (size of the basis set, treatment of relativistic effects, and treatment of electron correlation) on the calculated $W_A$ coefficient is investigated and a recommended value of 147.7 Hz with an estimated uncertainty of 1.5% is proposed.

physics.atom-ph

The Gregory-Newton Problem for Kissing Sticky Spheres

All possible non-isomorphic arrangements of 12 spheres kissing a central sphere (the Gregory-Newton problem) are obtained for the sticky-hard-sphere (SHS) model, and subsequently projected by geometry optimization onto a set of structures derived from an attractive Lennard-Jones (LJ) type of potential. It is shown that all 737 derived SHS contact graphs corresponding to the 12 outer spheres are (edge-induced) subgraphs of the icosahedral graph. The most widely used LJ(6,12) potential has only one minimum structure corresponding to the ideal icosahedron where the 12 outer spheres do not touch each other. The point of symmetry breaking away from the icosahedral symmetry towards the SHS limit is obtained for general LJ($a,b$) potentials with exponents $a,b\in \mathbb{R}_+$. Only if the potential becomes very repulsive in the short-range, determined by the LJ hard-sphere radius $σ$, symmetry broken solutions are observed.

physics.atm-clus

From Sticky-Hard-Sphere to Lennard-Jones-Type Clusters

A relation $\mathcal{M}_{\mathrm{SHS}\to\mathrm{LJ}}$ between the set of non-isomorphic sticky hard sphere clusters $\mathcal{M}_\mathrm{SHS}$ and the sets of local energy minima $\mathcal{M}_{LJ}$ of the $(m,n)$-Lennard-Jones potential $V^\mathrm{LJ}_{mn}(r) = \frac{\varepsilon}{n-m} [ m r^{-n} - n r^{-m} ]$ is established. The number of nonisomorphic stable clusters depends strongly and nontrivially on both $m$ and $n$, and increases exponentially with increasing cluster size $N$ for $N \gtrsim 10$. While the map from $\mathcal{M}_\mathrm{SHS}\to \mathcal{M}_{\mathrm{SHS}\to\mathrm{LJ}}$ is non-injective and non-surjective, the number of Lennard-Jones structures missing from the map is relatively small for cluster sizes up to $N=13$, and most of the missing structures correspond to energetically unfavourable minima even for fairly low $(m,n)$. Furthermore, even the softest Lennard-Jones potential predicts that the coordination of 13 spheres around a central sphere is problematic (the Gregory-Newton problem). A more realistic extended Lennard-Jones potential chosen from coupled-cluster calculations for a rare gas dimer leads to a substantial increase in the number of nonisomorphic clusters, even though the potential curve is very similar to a (6,12)-Lennard-Jones potential.

physics.atm-clus