Spin-Orbit Interaction and LS Coupling - Fine Structure - Hund’S Rules - Magnetic Susceptibilities
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Magnetism, Angular Momentum, and Spin
Chapter 19 Magnetism, Angular Momentum, and Spin P. J. Grandinetti Chem. 4300 P. J. Grandinetti Chapter 19: Magnetism, Angular Momentum, and Spin In 1820 Hans Christian Ørsted discovered that electric current produces a magnetic field that deflects compass needle from magnetic north, establishing first direct connection between fields of electricity and magnetism. P. J. Grandinetti Chapter 19: Magnetism, Angular Momentum, and Spin Biot-Savart Law Jean-Baptiste Biot and Félix Savart worked out that magnetic field, B⃗, produced at distance r away from section of wire of length dl carrying steady current I is 휇 I d⃗l × ⃗r dB⃗ = 0 Biot-Savart law 4휋 r3 Direction of magnetic field vector is given by “right-hand” rule: if you point thumb of your right hand along direction of current then your fingers will curl in direction of magnetic field. current P. J. Grandinetti Chapter 19: Magnetism, Angular Momentum, and Spin Microscopic Origins of Magnetism Shortly after Biot and Savart, Ampére suggested that magnetism in matter arises from a multitude of ring currents circulating at atomic and molecular scale. André-Marie Ampére 1775 - 1836 P. J. Grandinetti Chapter 19: Magnetism, Angular Momentum, and Spin Magnetic dipole moment from current loop Current flowing in flat loop of wire with area A will generate magnetic field magnetic which, at distance much larger than radius, r, appears identical to field dipole produced by point magnetic dipole with strength of radius 휇 = | ⃗휇| = I ⋅ A current Example What is magnetic dipole moment induced by e* in circular orbit of radius r with linear velocity v? * 휋 Solution: For e with linear velocity of v the time for one orbit is torbit = 2 r_v. -
Chapter 8 2013
described by Core Chapter 8 Electrons Wave Function e- filling spdf electronic configuration comprising (Orbital) Valence determined by Electrons described by Aufbau basis for Rules Periodic Quantum which involve Table Numbers which summarizes Orbital Pauli Hund’s which are Energy Exclusion Rule Periodic Properties Electron Configuration and Chemical Periodicity Quantum 4-quantum numbers specify the energy and location of Numbers electrons around a nucleus (all we can know). This numbers are the framework for the “electronic structure Orbital size of an atom”. Principal define & energy n = 1,2,3,.. s defines Name Symbol Permitted Values Property principal n positive integers (1,2,3...) orbital energy (size) Angular Orbital angular l orbital shape (0, 1, 2, and 3 momentum, l defines momentum integers from 0 to n-1 correspond to s, p, d, and f shape orbitals, respectively.) Magnetic Orbital magnetic integers from -l to 0 to +l orbital orientation in space defines ml ml orientation direction of e- spin spin m +1/2 or -1/2 Electron s Spin, ms defines spin Quantum Allowed Schrodinger’s equation gives an exact solution for H- Possible Orbitals Number Values atom, but does not for many electron-atoms. Electron- n Positive integers 1 2 3 electron repulsion in multi-electron split energy levels. 1,2,3,4.... Hydrogen Atom Multi-electron atoms 0 0 1 0 1 2 l 0 up to max Orbitals are of n-1 “degenerate” or Energy the same energy in Hydrogen! ml -l,...0...+l 0 0 -1 0 1 0 -1 0 1 -2-1 0 12 Orbital Name 1s 2s 2p 3s 3p 3d Electrons will Shapes or Boundry fill lowest Surface Plots energy orbitals first! Inner core electrons “shield” or “screen” outer 4-quantum numbers specify all the information we can know the energy electrons from the positive charge of the nucleus. -
1 Introduction 2 Spins As Quantized Magnetic Moments
Spin 1 Introduction For the past few weeks you have been learning about the mathematical and algorithmic background of quantum computation. Over the course of the next couple of lectures, we'll discuss the physics of making measurements and performing qubit operations in an actual system. In particular we consider nuclear magnetic resonance (NMR). Before we get there, though, we'll discuss a very famous experiment by Stern and Gerlach. 2 Spins as quantized magnetic moments The quantum two level system is, in many ways, the simplest quantum system that displays interesting behavior (this is a very subjective statement!). Before diving into the physics of two-level systems, a little on the history of the canonical example: electron spin. In 1921, Stern proposed an experiment to distinguish between Larmor's classical theory of the atom and Sommerfeld's quantum theory. Each theory predicted that the atom should have a magnetic moment (i.e., it should act like a small bar magnet). However, Larmor predicted that this magnetic moment could be oriented along any direction in space, while Sommerfeld (with help from Bohr) predicted that the orientation could only be in one of two directions (in this case, aligned or anti-aligned with a magnetic field). Stern's idea was to use the fact that magnetic moments experience a linear force when placed in a magnetic field gradient. To see this, not that the potential energy of a magnetic dipole in a magnetic field is given by: U = −~µ · B~ Here, ~µ is the vector indicating the magnitude and direction of the magnetic moment. -
Spin the Evidence of Intrinsic Angular Momentum Or Spin and Its
Spin The evidence of intrinsic angular momentum or spin and its associated magnetic moment came through experiments by Stern and Gerlach and works of Goudsmit and Uhlenbeck. The spin is called intrinsic since, unlike orbital angular momentum which is extrinsic, it is carried by point particle in addition to its orbital angular momentum and has nothing to do with motion in space. The magnetic moment ~µ of silver atom was measured in 1922 experiment by Stern and Gerlach and its projection µz in the direction of magnetic fieldz ^ B (through which the silver beam was passed) was found to be just −|~µj and +j~µj instead of continuously varying between these two as limits. Classically, magnetic moment is proportional to the angular momentum (12) and, assuming this proportionality to survive in quantum mechanics, quan- tization of magnetic moment leads to quantization of corresponding angular momentum S, which we called spin, q q µ = g S ) µ = g ~ m (57) z 2m z z 2m s as is the case with orbital angular momentum, where the ratio q=2m is called Bohr mag- neton, µb and g is known as Lande-g factor or gyromagnetic factor. The g-factor is 1 for orbital angular momentum and hence corresponding magnetic moment is l µb (where l is integer orbital angular momentum quantum number). A surprising feature here is that spin magnetic moment is also µb instead of µb=2 as one would naively expect. So it turns out g = 2 for spin { an effect that can only be understood if linearization of Schr¨odinger equation is attempted i.e. -
Fundamental Nature of the Fine-Structure Constant Michael Sherbon
Fundamental Nature of the Fine-Structure Constant Michael Sherbon To cite this version: Michael Sherbon. Fundamental Nature of the Fine-Structure Constant. International Journal of Physical Research , Science Publishing Corporation 2014, 2 (1), pp.1-9. 10.14419/ijpr.v2i1.1817. hal-01304522 HAL Id: hal-01304522 https://hal.archives-ouvertes.fr/hal-01304522 Submitted on 19 Apr 2016 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution| 4.0 International License Fundamental Nature of the Fine-Structure Constant Michael A. Sherbon Case Western Reserve University Alumnus E-mail: michael:sherbon@case:edu January 17, 2014 Abstract Arnold Sommerfeld introduced the fine-structure constant that determines the strength of the electromagnetic interaction. Following Sommerfeld, Wolfgang Pauli left several clues to calculating the fine-structure constant with his research on Johannes Kepler’s view of nature and Pythagorean geometry. The Laplace limit of Kepler’s equation in classical mechanics, the Bohr-Sommerfeld model of the hydrogen atom and Julian Schwinger’s research enable a calculation of the electron magnetic moment anomaly. Considerations of fundamental lengths such as the charge radius of the proton and mass ratios suggest some further foundational interpretations of quantum electrodynamics. -
7. Examples of Magnetic Energy Diagrams. P.1. April 16, 2002 7
7. Examples of Magnetic Energy Diagrams. There are several very important cases of electron spin magnetic energy diagrams to examine in detail, because they appear repeatedly in many photochemical systems. The fundamental magnetic energy diagrams are those for a single electron spin at zero and high field and two correlated electron spins at zero and high field. The word correlated will be defined more precisely later, but for now we use it in the sense that the electron spins are correlated by electron exchange interactions and are thereby required to maintain a strict phase relationship. Under these circumstances, the terms singlet and triplet are meaningful in discussing magnetic resonance and chemical reactivity. From these fundamental cases the magnetic energy diagram for coupling of a single electron spin with a nuclear spin (we shall consider only couplings with nuclei with spin 1/2) at zero and high field and the coupling of two correlated electron spins with a nuclear spin are readily derived and extended to the more complicated (and more realistic) cases of couplings of electron spins to more than one nucleus or to magnetic moments generated from other sources (spin orbit coupling, spin lattice coupling, spin photon coupling, etc.). Magentic Energy Diagram for A Single Electron Spin and Two Coupled Electron Spins. Zero Field. Figure 14 displays the magnetic energy level diagram for the two fundamental cases of : (1) a single electron spin, a doublet or D state and (2) two correlated electron spins, which may be a triplet, T, or singlet, S state. In zero field (ignoring the electron exchange interaction and only considering the magnetic interactions) all of the magnetic energy levels are degenerate because there is no preferred orientation of the angular momentum and therefore no preferred orientation of the magnetic moment due to spin. -
Dirac's Fine-Structure Formula for an “Abnormally High”
Dirac’s fine-structure formula for an “abnormally high” nuclear charge The solution of an old riddle A. LOINGER Dipartimento di Fisica dell’Università di Milano Via Celoria, 16 − 20133 Milano, Italy Summary. − In Dirac’s fine-structure formula for the hydrogenlike atoms a critical role is played by the square root of the following expression: the unity minus the square of the product of the atomic number by the fine-structure constant (which is approximately equal to 1/137). Indeed, for a fictitious, ideal nucleus for which the above product is greater than or equal to one, the mentioned square root becomes imaginary, or zero. I prove in this Note that the origin of such theoretical “breaking down” is quite simple and is inherent in the special theory of relativity of classical physics. PACS 11.10 − Relativistic wave equations; 03.65 – Semiclassical theories and applications. 1. − The problem As is well known, Dirac’s fine-structure formula for the energy of an electron in the Coulomb field generated by a fixed nuclear charge Ze is as follows: −1 2 2 2 E Z α (1.1) = 1+ , 2 2 m0c 2 2 2 1 2 []nr + (κ − Z α ) 2 where: E = W + m0c is the relativistic total energy; m0 is the rest-mass of the 2 electron; α := e (hc) is the fine-structure constant; nr = 0,1,2,3,... is the radial quantum number; κ = ±1,±2,±3,... is the auxiliary quantum number (according to a Weylian terminology); when nr = 0 , the quantum κ takes only the positive values [1]. -
The Fine Structure Constant
GENERAL ⎜ ARTICLE The Fine Structure Constant Biman Nath The article discusses the importance of the fine structure constant in quantum mechanics, along with the brief history of how it emerged. Al- though Sommerfelds idea of elliptical orbits has been replaced by wave mechanics, the fine struc- ture constant he introduced has remained as an Biman Nath is an important parameter in the field of atomic struc- astrophysicist at the ture. Raman Research Institute, Bengaluru. The values of the constants of Nature, such as Newton’s gravitational constant ‘G’, determine the nature of our Universe. Among these constants, there are a few which are pure numbers and have no units. For example, there is the ‘fine structure constant’, denoted by α, which has a value roughly 1/137. The value of α is related to the electromagnetic force between subatomic charged parti- cles, and essentially determines how an atom holds to- gether its electrons. It is however not obvious why this constant has this par- ticular value. Why 1/137 and not some other value? One might think the question is meaningless, but it is not. If the value of this constant had been slightly smaller or larger, even by as little as 4%, then stars would not have been able to sustain the nuclear reac- tions in their core that produce carbon. As a result, there would not have been any carbon-based lifeforms in our Universe. Therefore, the question why α ≈ 1/137 is not completely irrelevant. Scientists have even wondered if its value remains a con- stant over time. -
Importance of Hydrogen Atom
Hydrogen Atom Dragica Vasileska Arizona State University Importance of Hydrogen Atom • Hydrogen is the simplest atom • The quantum numbers used to characterize the allowed states of hydrogen can also be used to describe (approximately) the allowed states of more complex atoms – This enables us to understand the periodic table • The hydrogen atom is an ideal system for performing precise comparisons of theory and experiment – Also for improving our understanding of atomic structure • Much of what we know about the hydrogen atom can be extended to other single-electron ions – For example, He+ and Li2+ Early Models of the Atom • ’ J.J. Thomson s model of the atom – A volume of positive charge – Electrons embedded throughout the volume • ’ A change from Newton s model of the atom as a tiny, hard, indestructible sphere “ ” watermelon model Experimental tests Expect: 1. Mostly small angle scattering 2. No backward scattering events Results: 1. Mostly small scattering events 2. Several backward scatterings!!! Early Models of the Atom • ’ Rutherford s model – Planetary model – Based on results of thin foil experiments – Positive charge is concentrated in the center of the atom, called the nucleus – Electrons orbit the nucleus like planets orbit the sun ’ Problem: Rutherford s model “ ” ’ × – The size of the atom in Rutherford s model is about 1.0 10 10 m. (a) Determine the attractive electrical force between an electron and a proton separated by this distance. (b) Determine (in eV) the electrical potential energy of the atom. “ ” ’ × – The size of the atom in Rutherford s model is about 1.0 10 10 m. (a) Determine the attractive electrical force between an electron and a proton separated by this distance. -
Ultrasoft Pseudopotentials for Lanthanide Solvation Complexes: Core Or Valence Character of the 4F Electrons Rodolphe Pollet, C
Ultrasoft pseudopotentials for lanthanide solvation complexes: Core or valence character of the 4f electrons Rodolphe Pollet, C. Clavaguéra, J.-P. Dognon To cite this version: Rodolphe Pollet, C. Clavaguéra, J.-P. Dognon. Ultrasoft pseudopotentials for lanthanide solvation complexes: Core or valence character of the 4f electrons. Journal of Chemical Physics, American Institute of Physics, 2006, 124, pp.164103 - 1-6. 10.1063/1.2191498. hal-00083928 HAL Id: hal-00083928 https://hal.archives-ouvertes.fr/hal-00083928 Submitted on 21 Jul 2006 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Ultrasoft pseudopotentials for lanthanide solvation complexes: Core or valence character of the 4f electrons Rodolphe Pollet,∗ Carine Clavagu´era, Jean-Pierre Dognon Theoretical Chemistry Laboratory DSM/DRECAM/SPAM-LFP (CEA-CNRS URA2453) CEA/SACLAY, Bat. 522, 91191 GIF SUR YVETTE, FRANCE March 6, 2006 Abstract The 4f electrons of lanthanides, because of their strong localiza- tion in the region around the nucleus, are traditionally included in a pseudopotential core. This approximation is scrutinized by optimizing 3+ the structures and calculating the interaction energies of Gd (H2O) 3+ and Gd (NH3) microsolvation complexes within plane wave PBE cal- culations using ultrasoft pseudopotentials where the 4f electrons are included either in the core or in the valence space. -
Magnetism of Atoms and Ions
Magnetism of Atoms and Ions Wulf Wulfhekel Physikalisches Institut, Karlsruhe Institute of Technology (KIT) Wolfgang Gaede Str. 1, D-76131 Karlsruhe 1 0. Overview Literature J.M.D. Coey, Magnetism and Magnetic Materials, Cambridge University Press, 628 pages (2010). Very detailed Stephen J. Blundell, Magnetism in Condensed Matter, Oxford University Press, 256 pages (2001). Easy to read, gives a condensed overview C. Kittel, Introduction to Solid State Physics, John Whiley and Sons (2005). Solid state aspects 2 0. Overview Chapters of the two lectures 1. A quick refresh of quantum mechanics 2. The Hydrogen problem, orbital and spin angular momentum 3. Multi electron systems 4. Paramagnetism 5. Dynamics of magnetic moments and EPR 6. Crystal fields and zero field splitting 7. Magnetization curves with crystal fields 3 1. A quick refresh of quantum mechanics The equation of motion The Hamilton function: with T the kinetic energy and V the potential, q the positions and p the momenta gives the equations of motion: Hamiltonian gives second order differential equation of motion and thus p(t) and q(t) Initial conditions needed for Classical equations need information on the past! t p q 4 1. A quick refresh of quantum mechanics The Schrödinger equation Quantum mechanics replacement rules for Hamiltonian: Equation of motion transforms into Schrödinger equation: Schrödinger equation operates on wave function (complex field in space) and is of first order in time. Absolute square of the wave function is the probability density to find the particle at selected position and time. t Initial conditions needed for Schrödinger equation does not need information on the past! How is that possible? We know that the past influences the present! q 5 1. -
2.5. the Fine Structure of a Hydrogen Atom
Phys460.nb 33 0 0 0= ψ a A H'-H'A ψb = (2.281) 0 0 0 0 0 0 0 0 0 0 ψa A H' ψb - ψ a H'A ψb =A a ψa H' ψb -A b ψa H' ψb =(A a -A b) ψa H' ψb 0 0 If Aa ≠A b, this equation means that ψa H' ψb = 0. 0 0 For this situation, although we have a degeneracy, one can just do non-degenerate perturbation for ψa and ψb (separately) and there will be no singularities at all. 2.5. the fine structure of a hydrogen atom 2.5.1. Relativistic correction In QMI, we solved an ideal model for a hydrogen atom (i.e. a particle in 1/r potential). In a real hydrogen atom, that model missed some of the physics, and one of them is relativistic effects. Q: what is the energy of a particle, if the particle is moving at speed v and the rest mass m. m E=Mc 2 = c2 2 (2.282) 1- v c2 Q: what is the momentum of a particle, if the particle is moving at speed v and the rest mass m. m p =Mv= v 2 (2.283) 1- v c2 As a result, E= p2 c2 +m 2 c4 (2.284) To prove this relation, we start from the r.h.s., p2 c2 +m 2 c4 = v2 2 2 2 2 2 m2 c41- 2 2 2 2 4 2 2 2 2 4 m v m v c c2 m v c +m c -m c v m c m (2.285) c2 +m 2 c4 = + = = = c2 =E v2 v2 v2 v2 v2 1- 2 1- 2 1- 2 1- 2 1- 2 2 c c c c c 1- v c2 This relation between E and p is an very important relation for relativistic physics! Q: what is kinetic energy? A: First, find the energy of a particle when it is not moving p = 0.