Chemistry 1000 Lecture 8: Multielectron Atoms
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Density Functional Theory
Density Functional Theory Fundamentals Video V.i Density Functional Theory: New Developments Donald G. Truhlar Department of Chemistry, University of Minnesota Support: AFOSR, NSF, EMSL Why is electronic structure theory important? Most of the information we want to know about chemistry is in the electron density and electronic energy. dipole moment, Born-Oppenheimer charge distribution, approximation 1927 ... potential energy surface molecular geometry barrier heights bond energies spectra How do we calculate the electronic structure? Example: electronic structure of benzene (42 electrons) Erwin Schrödinger 1925 — wave function theory All the information is contained in the wave function, an antisymmetric function of 126 coordinates and 42 electronic spin components. Theoretical Musings! ● Ψ is complicated. ● Difficult to interpret. ● Can we simplify things? 1/2 ● Ψ has strange units: (prob. density) , ● Can we not use a physical observable? ● What particular physical observable is useful? ● Physical observable that allows us to construct the Hamiltonian a priori. How do we calculate the electronic structure? Example: electronic structure of benzene (42 electrons) Erwin Schrödinger 1925 — wave function theory All the information is contained in the wave function, an antisymmetric function of 126 coordinates and 42 electronic spin components. Pierre Hohenberg and Walter Kohn 1964 — density functional theory All the information is contained in the density, a simple function of 3 coordinates. Electronic structure (continued) Erwin Schrödinger -
Electron Density Functions for Simple Molecules (Chemical Bonding/Excited States) RALPH G
Proc. Natl. Acad. Sci. USA Vol. 77, No. 4, pp. 1725-1727, April 1980 Chemistry Electron density functions for simple molecules (chemical bonding/excited states) RALPH G. PEARSON AND WILLIAM E. PALKE Department of Chemistry, University of California, Santa Barbara, California 93106 Contributed by Ralph G. Pearson, January 8, 1980 ABSTRACT Trial electron density functions have some If each component of the charge density is centered on a conceptual and computational advantages over wave functions. single point, the calculation of the potential energy is made The properties of some simple density functions for H+2 and H2 are examined. It appears that for a diatomic molecule a good much easier. However, the kinetic energy is often difficult to density function would be given by p = N(A2 + B2), in which calculate for densities containing several one-center terms. For A and B are short sums of s, p, d, etc. orbitals centered on each a wave function that is composed of one orbital, the kinetic nucleus. Some examples are also given for electron densities that energy can be written in terms of the electron density as are appropriate for excited states. T = 1/8 (VP)2dr [5] Primarily because of the work of Hohenberg, Kohn, and Sham p (1, 2), there has been great interest in studying quantum me- and in most cases this integral was evaluated numerically in chanical problems by using the electron density function rather cylindrical coordinates. The X integral was trivial in every case, than the wave function as a means of approach. Examples of and the z and r integrations were carried out via two-dimen- the use of the electron density include studies of chemical sional Gaussian bonding in molecules (3, 4), solid state properties (5), inter- quadrature. -
Electron Charge Density: a Clue from Quantum Chemistry for Quantum Foundations
Electron Charge Density: A Clue from Quantum Chemistry for Quantum Foundations Charles T. Sebens California Institute of Technology arXiv v.2 June 24, 2021 Forthcoming in Foundations of Physics Abstract Within quantum chemistry, the electron clouds that surround nuclei in atoms and molecules are sometimes treated as clouds of probability and sometimes as clouds of charge. These two roles, tracing back to Schr¨odingerand Born, are in tension with one another but are not incompatible. Schr¨odinger'sidea that the nucleus of an atom is surrounded by a spread-out electron charge density is supported by a variety of evidence from quantum chemistry, including two methods that are used to determine atomic and molecular structure: the Hartree-Fock method and density functional theory. Taking this evidence as a clue to the foundations of quantum physics, Schr¨odinger'selectron charge density can be incorporated into many different interpretations of quantum mechanics (and extensions of such interpretations to quantum field theory). Contents 1 Introduction2 2 Probability Density and Charge Density3 3 Charge Density in Quantum Chemistry9 3.1 The Hartree-Fock Method . 10 arXiv:2105.11988v2 [quant-ph] 24 Jun 2021 3.2 Density Functional Theory . 20 3.3 Further Evidence . 25 4 Charge Density in Quantum Foundations 26 4.1 GRW Theory . 26 4.2 The Many-Worlds Interpretation . 29 4.3 Bohmian Mechanics and Other Particle Interpretations . 31 4.4 Quantum Field Theory . 33 5 Conclusion 35 1 1 Introduction Despite the massive progress that has been made in physics, the composition of the atom remains unsettled. J. J. Thomson [1] famously advocated a \plum pudding" model where electrons are seen as tiny negative charges inside a sphere of uniformly distributed positive charge (like the raisins|once called \plums"|suspended in a plum pudding). -
Nature of Noncovalent Carbon-Bonding Interactions Derived from Experimental Charge-Density Analysis
Nature of Noncovalent Carbon-Bonding Interactions Derived from Experimental Charge-Density Analysis Eduardo C. Escudero-Adán, Antonio Bauzffl, Antonio Frontera, and Pablo Ballester E. C. Escudero-Adán,+ Prof. P. Ballester X-Ray Diffraction Unit Institute of Chemical Research of Catalonia (ICIQ) Avgda. Països Catalans 16, 43007 Tarragona (Spain) E-mail : [email protected] A. Bauzffl,+ Prof. A. Frontera Department of Chemistry Universitat de les Illes Balears Crta. de Valldemossa km 7.5, 07122 Palma de Mallorca (Spain) E-mail : [email protected] Prof. P. Ballester Catalan Institution for Research and Advanced Studies (ICREA) Passeig Lluïs Companys 23, 08010 Barcelona (Spain) In an effort to better understand the nature of noncovalent carbon-bonding interactions, we undertook accurate high-res- olution X-ray diffraction analysis of single crystals of 1,1,2,2-tet- racyanocyclopropane. We selected this compound to study the fundamental characteristics of carbon-bonding interactions, because it provides accessible s holes. The study required ex- tremely accurate experimental diffraction data, because the in- teraction of interest is weak. The electron-density distribution around the carbon nuclei, as shown by the experimental maps of the electrophilic bowl defined by a (CN)2C-C(CN)2 unit, was assigned as the origin of the interaction. This fact was also evidenced by plotting the D21(r) distribution. Taken together, the obtained results clearly indicate that noncovalent carbon bonding can be explained as an interaction between confront- ed oppositely polarized regions. The interaction is, thus elec- trophilic–nucleophilic (electrostatic) in nature and unambigu- ously considered as attractive. Attractive intermolecular electrostatic interactions encompass electron-rich and electron-poor regions of two molecules that complement each other.[1] Electron-rich entities are typically anions or lone-pair electrons and the most well-known elec- tron-poor entity is the hydrogen atom. -
10 Mar 2015 Density Functional Theory for Field Theorists I
RUNHETC-2015-07 SCIPP 15/11 Density Functional Theory for Field Theorists I Tom Banks NHETC and Department of Physics Rutgers University, Piscataway, NJ 08854-8019 and Department of Physics and SCIPP University of California, Santa Cruz, CA 95064 E-mail: [email protected] Abstract I summarize Density Functional Theory (DFT) in a language familiar to quantum field theorists, and introduce several apparently novel ideas for constructing systematic approximations for the density functional. I also note that, at least within the large K approximation (K is the number of electron spin components), it is easier to compute the quantum effective action of the Coulomb photon field, which is related to the density functional by algebraic manipulations in momentum space. arXiv:1503.02925v1 [cond-mat.mtrl-sci] 10 Mar 2015 0 Contents 1 Density Functional Theory for Quantum Field Theorists 1 2 Expansions in the Number of Spin Components 5 2.1 The Large K Expansion ............................. 5 2.2 SmallKExpansion ................................ 8 2.3 TheKSEquations ................................ 9 3 Expansions of the Functional Determinant 10 4 1/K expansion of the HEG 11 5 Conclusions 12 6 Acknowledgments 13 1 Density Functional Theory for Quantum Field The- orists Much of atomic, molecular and (quantum) condensed matter physics, reduces, in the non- relativistic limit, to the problem of solving the Schr¨odinger equation for point-like nuclei and electrons, interacting via the Coulomb potential. The electrons are fermions, and are best treated by introducing an electron field ik x ψi(x)= ai(k)e · , (1.1) Xk where i is a spin label. If we introduce dimensionless space-time coordinates, by using the Bohr radius to measure length, and the Rydberg to measure energy, the only parameters in me the problem are the nuclear charges Za and the mass ratios ma . -
Density Functional Theory
NEA/NSC/R(2015)5 Chapter 12. Density functional theory M. Freyss CEA, DEN, DEC, Centre de Cadarache, France Abstract This chapter gives an introduction to first-principles electronic structure calculations based on the density functional theory (DFT). Electronic structure calculations have a crucial importance in the multi-scale modelling scheme of materials: not only do they enable one to accurately determine physical and chemical properties of materials, they also provide data for the adjustment of parameters (or potentials) in higher-scale methods such as classical molecular dynamics, kinetic Monte Carlo, cluster dynamics, etc. Most of the properties of a solid depend on the behaviour of its electrons, and in order to model or predict them it is necessary to have an accurate method to compute the electronic structure. DFT is based on quantum theory and does not make use of any adjustable or empirical parameter: the only input data are the atomic number of the constituent atoms and some initial structural information. The complicated many-body problem of interacting electrons is replaced by an equivalent single electron problem, in which each electron is moving in an effective potential. DFT has been successfully applied to the determination of structural or dynamical properties (lattice structure, charge density, magnetisation, phonon spectra, etc.) of a wide variety of solids. Its efficiency was acknowledged by the attribution of the Nobel Prize in Chemistry in 1998 to one of its authors, Walter Kohn. A particular attention is given in this chapter to the ability of DFT to model the physical properties of nuclear materials such as actinide compounds. -
Electronic Structure and Physical Properties of 13C Carbon Composite
Electronic structure and physical properties of 13C carbon composite ABSTRACT: This review is devoted to the application of graphite and graphite composites in science and technology. Structure and electrical properties, as so technological aspects of producing of high-strength artificial graphite and dynamics of its destruction are considered. These type of graphite are traditionally used in the nuclear industry. Author was focused on the properties of graphite composites based on carbon isotope 13C. Generally, the review relies on the original results and concentrates on actual problems of application and testing of graphite materials in modern nuclear physics and science and its technology applications. Translated by author from chapters 5 of the Russian monograph by Zhmurikov E.I., Bubnenkov I.A., Pokrovsky A.S. et al. Graphite in Science and Nuclear Technique// eprint arXiv:1307.1869, 07/2013 (BC 2013arXiv1307.1869Z Author: Evgenij I. Zhmurikov Address: 68600 Pietarsaari, Finland E-mail: [email protected] KEYWORDS: Structure and properties of carbon; Isotope 13C; Radioactive ion beams 2 1. Introduction In order to explore ever-more exotic regions of the nuclear chart, towards the limits of stability of nuclei, European nuclear physicists have built several large-scale facilities in various countries of the European Union. Today they are collaborating in planning of a new radioactive ion beam (RIB) facility which will permit them to investigate hitherto unreachable parts of the nuclear chart. This European ISOL (isotope-separation-on-line) facility is called EURISOL [1]. At the present moment experiments with RIB of the first generation have yielded important results. But the first generation RIB facilities are often limited by the low intensity of the beams. -
Theoretical Basis of Quantum-Mechanical Modeling of Functional Nanostructures
S S symmetry Review Theoretical Basis of Quantum-Mechanical Modeling of Functional Nanostructures Aleksey Fedotov 1,2 , Alexander Vakhrushev 1,2,*, Olesya Severyukhina 1,2, Anatolie Sidorenko 2 , Yuri Savva 2, Nikolay Klenov 3,4 and Igor Soloviev 3 1 Department Simulation and Synthesis Technology Structures, Institute of Mechanics, Udmurt Federal Research Center of the Ural Branch of the Russian Academy of Sciences, 426067 Izhevsk, Russia; [email protected] (A.F.); [email protected] (O.S.) 2 Laboratory of Functional Nanostructures, Orel State University named after I.S. Turgenev, 302026 Orel, Russia; [email protected] (A.S.); su_fi[email protected] (Y.S.) 3 Laboratory of Nanostructure Physics, Department of Microelectronics, Skobeltsyn Institute of Nuclear Physics, Lomonosov Moscow State University, 119991 Moscow, Russia; [email protected] (N.K.); [email protected] (I.S.) 4 Science and Research Department, Moscow Technical University of Communication and Informatics, 111024 Moscow, Russia * Correspondence: [email protected] Abstract: The paper presents an analytical review of theoretical methods for modeling functional nanostructures. The main evolutionary changes in the approaches of quantum-mechanical modeling are described. The foundations of the first-principal theory are considered, including the stationery and time-dependent Schrödinger equations, wave functions, the form of writing energy operators, and the principles of solving equations. The idea and specifics of describing the motion and inter- action of nuclei and electrons in the framework of the theory of the electron density functional are Citation: Fedotov, A.; Vakhrushev, A.; Severyukhina, O.; Sidorenko, A.; presented. Common approximations and approaches in the methods of quantum mechanics are Savva, Y.; Klenov, N.; Soloviev, I. -
The Radial Electron Density in the Hydrogen Atom and the Model of Oscillations in a Chain System
July, 2012 PROGRESS IN PHYSICS Volume 3 The Radial Electron Density in the Hydrogen Atom and the Model of Oscillations in a Chain System Andreas Ries Universidade Federal de Pernambuco, Centro de Tecnologia e Geociencias,ˆ Laboratorio´ de Dispositivos e Nanoestruturas, Rua Academicoˆ Helio´ Ramos s/n, 50740-330 Recife – PE, Brazil E-mail: [email protected] The radial electron distribution in the Hydrogen atom was analyzed for the ground state and low-lying excited states by means of a fractal scaling model originally published by Muller¨ in this journal. It is shown that Muller’s¨ standard model is not fully adequate to fit these data and an additional phase shift must be introduced into its mathematical apparatus. With this extension, the radial expectation values could be expressed on the logarithmic number line by very short continued fractions where all numerators are Euler’s number. Within the rounding accuracy, no numerical differences between the expectation values (calculated from the wavefunctions)and the corresponding modeled values exist, so the model matches these quantum mechanical data exactly. Besides that, Muller’s¨ concept of proton resonance states can be transferred to electron resonances and the radial expectation values can be interpreted as both, proton resonance lengths and electron resonance lengths. The analyzed data point to the fact that Muller’s¨ model of oscillations in a chain system is compatible with quantum mechanics. 1 Introduction partial denominators are positive or negative integer values: The radial electron probability density in the Hydrogen atom 1 S = n + . (2) was analyzed by a new fractal scaling model, originally pub- 0 1 n + lished by Muller¨ [1–3] in this journal. -
Introduction to First-Principles Method
Joint ICTP/CAS/IAEA School & Workshop on Plasma-Materials Interaction in Fusion Devices, July 18-22, 2016, Hefei Introduction to First-Principles Method by Guang-Hong LU (吕广宏) Beihang University Computer Modeling & Simulation Theory ComputerComputer modeling & simulation” has Modeling emerged as an indespensableExperiment method for & scientificSimulation research of materials in parallel to experiment and theory. Outline Introduction (first principles) Introduction (history of first principles) Basic principles • calculation of total energy • electron-electron interaction (DFT-LDA) • Bloch’s theorem – periodic system • electron-ion interaction (pseudopotential) Supercell technique Computational procedure Future 3 Multiscale Modeling & Simulation: Conceptual framework First-principles method First-principles method Solve quantum mechanic Schrodinger equation to obtain Eigen value and Eigen function, and thus the electronic structure. • The charm: only atomic number and crystal structure as input, which can determine precisely the structure and the properties of the real materials. • first principles - physics, materials Density functional theory • ab initio -quantum chemistry Hartree-Fork self-consistent field A connection between atomic and macroscopic levels (不同尺度之间的联系) First-principles method Elastic constants Binding energy Energy barrier mechanics thermodynamics kinetics 7 Outline Introduction (first principles) Introduction (history of first principles) Basic principles • calculation of total energy • electron-electron interaction -
Quantum Mechanics
Quantum Mechanics • No real understanding of the chemical bond is possible in terms of classical mechanics because very small particles such as electrons do not obey the laws of classical mechanics. • Their behavior is determined by quantum mechanics, which was developed in the second half of the 1920s culminating in a mathematical formalism that we still use today. • Quantum mechanics is used by chemists as a tool to obtain the wave function and corresppgonding energy and ggyeometry of a molecule by solving the fundamental equation of quantum mechanics, called the Schrödinger equation. • The Schrödinger equation can only be completely solved for the hydrogen atom, or isoelectronic ions, with just one electron. Approximation methods must be used for multi‐ electron atoms and polyatomic molecules. • The most characteristic feature of quantum mechanics which differentiates it from classical mechanics is its probalistic character. Classical statistical Quantum probabilistic Dual Wave‐Particle Nature of Light • Light is not just emitted or absorbed in light quanta but that it travels through space as small bundles of energy called photons. • Although photons are regarded as mass‐less particles, their energy is remarkably expressed in terms of the frequency of a wave. • Although light has no mass it has momentum, which depends on the wavelength of the light. E = h . = c/ E = h . c / h / pde Broglie wavelength E = p.c (E = m.c2) Ephoton photon 1 / photon pphoton • In summary, the energy of light is transmitted in the form of particle‐like photons, which have an energy that depends of the frequency and momentum of the photon. -
A Chemical Interpretation of Protein Electron Density Maps in The
bioRxiv preprint doi: https://doi.org/10.1101/613109; this version posted April 18, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. A chemical interpretation of protein electron density maps in the worldwide protein data bank Sen Yao1,2,3 and Hunter N.B. Moseley1,2,3,4,5,* 1Department of Molecular & Cellular Biochemistry 2Markey Cancer Center 3Resource Center for Stable Isotope Resolved Metabolomics 4Institute for Biomedical Informatics 5Center for Clinical and Translational Science University of Kentucky, Lexington KY, United States *Corresponding Author: [email protected] Software and full results available at: https://github.com/MoseleyBioinformaticsLab/pdb_eda (software on GitHub) https://pypi.org/project/pdb-eda/ (software on PyPI) https://pdb-eda.readthedocs.io/en/latest/ (documentation on ReadTheDocs) https://doi.org/10.6084/m9.figshare.7994294 (code and results on FigShare) Abstract High-quality three-dimensional structural data is of great value for the functional interpretation of biomacromolecules, especially proteins; however, structural quality varies greatly across the entries in the worldwide Protein Data Bank (wwPDB). Since 2008, the wwPDB has required the inclusion of structure factors with the deposition of x-ray crystallographic structures to support the independent evaluation of structures with respect to the underlying experimental data used to derive those structures. However, interpreting the discrepancies between the structural model and its underlying electron density data is difficult, since derived electron density maps use arbitrary electron density units which are inconsistent between maps from different wwPDB entries.