New aspects of quantum electrodynamics on electronic structure and dynamics.

Application of Alpha-oscillator theory to quantum electrodynamics (QED) solves the mystery (Feynman) of the double-slit phenomenon involved in the foundation of quantum mechanics (QM). Even if with the same initial condition given, different spots on the screen can be predicted deterministically with no introduction of hidden variables. The interference pattern is similar to, but cannot be reproduced quantitatively by, that of the QM wave function, contrary to many-years-anticipation: a new prediction, awaiting experimental test over and above the Bohr-Einstein gedanken experiment.

Quantum simulation of nanosized materials: 100 years of mystery is solved.

Application of alpha-oscillator theory to quantum electrodynamics (QED) solves the mystery (as Feynman said) of the double-slit phenomenon involved in the foundation of quantum mechanics (QM). Even if with the same initial condition given, different spots on the screen can be predicted deterministically with no introduction of hidden variables. The general proof has already been published in Ref.

Theoretical study of lithium ionic conductors by electronic stress tensor density and electronic kinetic energy density.

We analyze the electronic structure of lithium ionic conductors, Li3PO4 and Li3PS4, using the electronic stress tensor density and kinetic energy density with special focus on the ionic bonds among them. We find that, as long as we examine the pattern of the eigenvalues of the electronic stress tensor density, we cannot distinguish between the ionic bonds and bonds among metalloid atoms. We then show that they can be distinguished by looking at the morphology of the electronic interface, the zero surface of the electronic kinetic energy density.

Electronic stress tensor analysis of molecules in gas phase of CVD process for GeSbTe alloy.

We analyze the electronic structure of molecules which may exist in gas phase of chemical vapor deposition process for GeSbTe alloy using the electronic stress tensor, with special focus on the chemical bonds between Ge, Sb, and Te atoms. We find that, from the viewpoint of the electronic stress tensor, they have intermediate properties between alkali metals and hydrocarbon molecules. We also study the correlation between the bond order which is defined based on the electronic stress tensor, and energy-related quantities.

On reversible bonding of hydrogen molecules on platinum clusters.

The local reactivity of hydrogenated platinum clusters (Pt clusters) has been studied using the regional density functional theory method. We observed that antibond orbitals constitute the preferable binding site for hydrogen molecules H(2). Those sites are characterized by lowered electronic chemical potential and strong directionality and exhibit electrophilic nature.

Electronic stress tensor description of chemical bonds using nonclassical bond order concept.

The stress tensors are used widely for description of internal forces of matter. For some time it is also applied in quantum theory in studies of molecular properties in chemical systems. Electronic stress tensors measure effects caused by internal forces acting on electrons in molecules and particularly those between bonded atoms.

Hydrogen dissociative chemisorption and desorption on saturated subnano palladium clusters (Pdn, n = 2-9).

H2 sequential dissociative chemisorption on small palladium clusters was studied using density functional theory. The chosen clusters Pdn (n = 2-9) are of the lowest energy structures for each n. H2 dissociative chemisorption and subsequent H atom migration on the bare Pd clusters were found to be nearly barrierless.

Physical nature of intermolecular interactions within cAMP-dependent protein kinase active site: differential transition state stabilization in phosphoryl transfer reaction.

The origin of enzyme catalytic activity may be effectively explored within the nonempirical theory of intermolecular interactions. The knowledge of electrostatic, exchange, delocalization, and correlation components of the transition state and substrates stabilization energy arising from each enzyme active site residue allows to examine the most essential physical effects involved in enzymatic catalysis. Consequently, one can build approximate models of the catalytic activity in a systematic and legitimate manner.

Use of nuclear stiffness in search for a maximum hardness principle and for the softest states along the chemical reaction path: a new formula for the energy third derivative gamma.

Nuclear stiffness, expressed as a hardness derivative, appears to be a good measure of the slope of global hardness. The authors analyze molecular states for which hardness has a maximum value. Maximum hardness principle (MHP) has been discussed.

The field theoretical study of chemical interaction in terms of the Rigged QED: new reactivity indices.

How the mode of bonding affects stability and reactivity of molecule on the frame of nonrelativistic limit of the rigged quantum electrodynamics using new indices for description of bond properties related to bond orders have been characterized here. These indices are in close relation with tensorial interpretation of bond that among others allows discriminating covalent bonds using spindle structure concept. The real three-dimensional space representation of new interaction energy density utilized in this study contribute to better understanding of interaction phenomena between atoms and molecules.

Nuclear reactivity indices within regional density functional theory.

Regional chemical potential values-mu(R) have been obtained with the use of nuclear reactivity indices. Perturbational formulae use values of reactivity indices of isolated molecular fragments. The changes of the parameters (DeltaN(R),{ DeltaQ(i)}i epsilonR) within each fragment determine the value of the regional chemical potential after a chemical reaction.

A new visualization scheme of chemical energy density and bonds in molecules.

Covalent bond describes electron pairing in between a pair of atoms and molecules. The space is partitioned in mutually disjoint regions by using a new concept of the electronic drop region R(D), atmosphere region R(A), and the interface S (Tachibana in J Chem Phys 115:3497-3518, 2001). The covalent bond formation is then characterized by a new concept of the spindle structure.