Calculation of band structure using group theory. Sudeep Kumar Ghosh, Department of Physics, Indian Institute of Science, Bangalore.

Similar documents
2.3 Band structure and lattice symmetries: example of diamond

5.5. Representations. Phys520.nb Definition N is called the dimensions of the representations The trivial presentation

M.S. Dresselhaus G. Dresselhaus A. Jorio. Group Theory. Application to the Physics of Condensed Matter. With 131 Figures and 219 Tables.

PROJECT C: ELECTRONIC BAND STRUCTURE IN A MODEL SEMICONDUCTOR

Chapter 5 Equations for Wave Function

Electrons in a weak periodic potential

Lecture. Ref. Ihn Ch. 3, Yu&Cardona Ch. 2

Chapter 1. Crystal structure. 1.1 Crystal lattices

Dirac semimetal in three dimensions

Group. Benzene D 6h z B B. E ( x y, xy) ( x, y) A B B C 2

Classical Theory of Harmonic Crystals

Representation Theory

SUPPLEMENTARY INFORMATION

Little Orthogonality Theorem (LOT)

Electrons in a periodic potential

I. Perturbation Theory and the Problem of Degeneracy[?,?,?]

The structure of liquids and glasses. The lattice and unit cell in 1D. The structure of crystalline materials. Describing condensed phase structures

ECE 535 Theory of Semiconductors and Semiconductor Devices Fall 2015 Homework # 5 Due Date: 11/17/2015

Translation Groups; Introduction to Bands and Reciprocal Space. Timothy Hughbanks, Texas A& M University

( ) ( ) SALCs as basis functions. LCAO-MO Theory. Rewriting the Schrödinger Eqn. Matrix form of Schrödinger Eqn. Hφ j. φ 1. φ 3. φ 2. φ j. φ i.

5 Irreducible representations

Tight Binding Method: Linear Combination of Atomic Orbitals (LCAO)

Physics 221A Fall 1996 Notes 16 Bloch s Theorem and Band Structure in One Dimension

Wavefunction and electronic struture in solids: Bloch functions, Fermi level and other concepts.

Bonding in solids The interaction of electrons in neighboring atoms of a solid serves the very important function of holding the crystal together.

Theoretical Concepts of Spin-Orbit Splitting

5 Symmetries and point group in a nut shell

Classification of Solids, Fermi Level and Conductivity in Metals Dr. Anurag Srivastava

Chapter 4 Symmetry and Chemical Bonding

Answers Quantum Chemistry NWI-MOL406 G. C. Groenenboom and G. A. de Wijs, HG00.307, 8:30-11:30, 21 jan 2014

Crystal field effect on atomic states

Chapter 4 Symmetry and Chemical Bonding

Notation. Irrep labels follow Mulliken s convention: A and B label nondegenerate E irreps, doubly T degenerate, triply degenerate

Chapter 1: Chemical Bonding

3: Many electrons. Orbital symmetries. l =2 1. m l

26 Group Theory Basics

Electrons responsible for the chemical properties of atoms Electrons in the outer energy level Valence electrons are the s and p electrons in the

Kronig-Penney model. 2m dx. Solutions can be found in region I and region II Match boundary conditions

Tight binding models from band representations

SUPPLEMENTARY INFORMATION

CHEM6085: Density Functional Theory

Review of Matrices. L A matrix is a rectangular array of numbers that combines with other such arrays according to specific rules.

2. Electronic Band Structures

Energy bands in two limits

Lecture 6. Tight-binding model

Quantum Condensed Matter Physics

obtained is essentially depends on the degeneracy of one-electron levels (on the degree of symmetry). The lower symmetry, the larger secular equation

Tight-Binding Approximation. Faculty of Physics UW

Spins and spin-orbit coupling in semiconductors, metals, and nanostructures

Chemical Bonding Ionic Bonding. Unit 1 Chapter 2

Condensed Matter Physics Prof. G. Rangarajan Department of Physics Indian Institute of Technology, Madras

Energy bands in solids. Some pictures are taken from Ashcroft and Mermin from Kittel from Mizutani and from several sources on the web.

Computer Algebraic Tools for Studying the Symmetry Properties of Molecules and Clusters. Katya Rykhlinskaya, University of Kassel

Lecture 4: Band theory

Introduction to Solid State Physics or the study of physical properties of matter in a solid phase

Modeling Transport in Heusler-based Spin Devices

Chem 728 Introduction to Solid Surfaces

The Gutzwiller Density Functional Theory

Nearly Free Electron Gas model - I

Physics of Materials: Classification of Solids On The basis of Geometry and Bonding (Intermolecular forces)

Translation Symmetry, Space Groups, Bloch functions, Fermi energy

Nearly-Free Electrons Model

structure of graphene and carbon nanotubes which forms the basis for many of their proposed applications in electronics.

Module 16. Diffusion in solids II. Lecture 16. Diffusion in solids II

Effective theory of quadratic degeneracies

Section 10 Metals: Electron Dynamics and Fermi Surfaces

Problem Set # 1 Solutions CHAPTERS 2 & 3 ATOMIC STRUCTURE AND INTERATOMIC BONDING and THE STRUCTURE OF CRYSTALLINE SOLIDS

Electronic Structure Theory for Periodic Systems: The Concepts. Christian Ratsch

Lecture 12. Symmetry Operations. NC State University

CHAPTER 2: ENERGY BANDS & CARRIER CONCENTRATION IN THERMAL EQUILIBRIUM. M.N.A. Halif & S.N. Sabki

Lecture 4: Basic elements of band theory

Molecular Symmetry 10/25/2018

Electronic structure of correlated electron systems. G.A.Sawatzky UBC Lecture

Chapter 7 Ionic and Metallic Bonding

Lecture 6 - Bonding in Crystals

Minimal Update of Solid State Physics

Class 27: Reciprocal Space 1: Introduction to Reciprocal Space

Supersymmetry and Quantum Hall effect in graphene

Little Orthogonality Theorem (LOT)

PAPER:2, PHYSICAL CHEMISTRY-I QUANTUM CHEMISTRY. Module No. 34. Hückel Molecular orbital Theory Application PART IV

Electrons in Crystals. Chris J. Pickard

Group Theory: Matrix Representation & Consequences of Symmetry

Select/Special Topics in Atomic Physics Prof. P.C. Deshmukh Department Of Physics Indian Institute of Technology, Madras

Ph/CS 219b. Exercises Due: Thursday 22 February 2018

Chemistry 543--Final Exam--Keiderling May 5, pm SES

A marks are for accuracy and are not given unless the relevant M mark has been given (M0 A1 is impossible!).

Chemistry 431. Lecture 14. Wave functions as a basis Diatomic molecules Polyatomic molecules Huckel theory. NC State University

Complex Numbers; Digression. Handouts - Download and Read! Cyclic Groups. Character Tables for Cyclic Groups

Group Theory and Its Applications in Physics

Berry s phase in Hall Effects and Topological Insulators

Physics 541: Condensed Matter Physics

Hückel Molecular orbital Theory Application PART III

Short Sample Solutions to the Sample Exam for (3rd Year Course 6) Hilary Term 2011

POEM: Physics of Emergent Materials

Introduction to Condensed Matter Physics

Nearly Free Electron Gas model - II

An introduction to magnetism in three parts

Ceramic Bonding. CaF 2 : large SiC: small

Supplementary Materials for

Condensed Matter Physics Prof. G. Rangarajan Department of Physics Indian Institute of Technology, Madras

Transcription:

Calculation of band structure using group theory Sudeep Kumar Ghosh, Department of Physics, Indian Institute of Science, Bangalore.

Plan of the talk Brief overview of the representation theory and the character system of a group. Brief overview of the Tight Binding Model and the Nearly Free Electron Model of band structure calculation. Discussion of the tight binding model and the formation of the secular determinant. Application of the Group Theory in simplifying the secular determinant for Beta Brass and explicit calculation. Calculation of the band structure of Tellurium using the Nearly Free Electron Approximation using the symmetry arguments from Group Theory. Concluding remarks.

Brief overview of the representation theory and the character system of a group Representation Reducible Irreducible Characters Uniquely describes a representation Within a representation uniquely describes an Equivalence Class

Useful theorems of Group Theory 1) Relation b/w dimension of irreps and order of a group : 2) Relation b/w functions associated with irreps and atomic orbitals: Where, is the function associated the ith irrep, are the atomic orbitals, is the character associated with the operator R in the ith irrep.

Basic idea of the Tight Binding model(tbm) and the Nearly Free Electron model(nfe) TBM: Atoms in lattice are far apart electrons in an atom are only affected by nearest or next nearest neighbors. Most useful in describing energy bands of transition metals(having partially filled d-shells) and electronic structure of insulators. NFE: Electrons are nearly free and perturbed only by a weak periodic potential of the ion-cores. Applicable to metals in groups of the periodic table(i.e. having atomic structure consisting of s and p electrons outside of a closed shell noble gas configuration.)

Generic way of TBM calculation Aim of energy band structure calculation determine E(k).One needs to solve the one electron Schroedinger eqn: where, is the periodic crystalline potential, are the Bloch wave functions with energy E & are the primitive translation vectors. Bloch Sum: Considering a simple crystal with one atom per unit cell the Bloch Sum of wave vector k is: where, is the AO of quantum no. i in the reference unit cell; is the same orbital of the atom in the unit cell and N is the no. of unit cells in the crystal.

Continued LCAO: Try the solution of the Schroedinger equation to be: where, are the coefficients of expansion. Secular Determinant: where, Now considering V(r)= + we can write: where, the AO is Eigen function of the H with energy.

Application of Group Theory to simplify the secular determinant for Beta Brass Unit cell has one Zinc atom and one Copper atom and SC lattice. Table:-1

Continued Table:-2 Ref:E.Wigner,Phys.Rev.,vol.50,pp.58-67,July 1,1936

Motivation to the Character Table Matrix representing E has the form and hence its order will equal the dimensionality of that representation. The cubic system has 10 classes and 48 operations; hence using Theorem-2 the characters for E are This is the only combination of 10 integers whose squares add up to 48. Interesting feature of character tables involving the inversion operation is that if the character table is divided into 4 blocks then 3 are identical and the 4 th one is the negative of the others. This leads to considerable simplification in the computation of the characters.

Explanation to the associated atomic orbitals in some of these representation The atomic orbitals can be expressed as: Conveniently expressed as: The five d functions (x,y,z). Cubic symmetry operations on a point with coordinates (x,y,z) will lead to the table as shown. can also be expressed as l.c of Table:-3

Continued Rerep. of E and must have chars 3 & -1 respectively. Since we can write for the matrix have the following form: Similarly, the full set of red. chars is: 3,-1,1,-1,0,-3,1,-1,1,0 which is identical to irrep. Since the orbitals are prop. to x,y,z respec. we say they belong to and are triply degenerate. Using the same logic we can see s,( ) and ( ) belong to and representations respectively. N.B: Due to crystal field splitting the 5 degenerate d-states have been split into a 2-fold and a 3-fold state.

Symmetry in the B.Z Along the axis( ) ;there only 4 symmetry operations in the group and the associated coord. transformations are: Table:-4 The character table is determined in the same way as before to be: Table:-5

The symmetry argument in B.Z for Beta-Brass(B.B) TBM calculation for B.B bases on the use of d functions since Cu and Zn both have ten 3d valence electrons. Neglecting Zn-Zn n.n int.,since the dist. b/w these 2 atoms in the alloy is much larger than that b/w 2 Cu atoms or b/w Cu-Zn neighbours,then the only nonvanishing field integrals are: Ref: J.C.Slater,Phys. Rev.,vol.94,pp.1498-1524,June 15,1954.

The 10 10 Secular Determinant

Rearranging Rows and Columns

Further simplification by group theory Table:-4 Table:-6 From Table:-6 applying Theorem-2 for the rep. of Table:-5 we have: Table:-6 So, xy and belong to.further, functions belonging to diff. irrep do not mix which is seen from the following vanishing integral:

Reduced Secular Determinant

Determination of degeneracies of the energy bands calculated by NFE for Te Cubic crystalline field splits the 5 fold d levels into a 3 fold and a 2 fold level. Expect removal of some degeneracies when a crystal field applied to the energies calculated using FE. Can be understood using group theory. For example, consider Tellurium(Te):

Consideration of the symmetries of the Te B.Z At the top of the B.Z the point A(0,0,π/c) the full symmetry group is: 1) E, the Identity; 2), a rotation about the z-axis, followed by a translation c/3 along the axis. 3) A 4) B,followed by a translation c/3. 5),followed by no translation. 6),followed by a translation c/3. 7) T, a displacement of c along the z-axis. Note:

Cayley table and character table Table:-7 Table:-8

Symmetry along the Δ-axis of Te Both rotational and translational symmetries are present. For the rotational part the symmetry operations are, and rotations. They form an abelian group and the characters associated with them are the cube roots of unity, which are where.. The translational characters have the form. Hence for the direct product representation the character table is: Table:-9

Concept of compatibility Basic Idea: The symmetry of the wave functions at Γ and at some adjacent point on the Δ-axis must bear some relation to one another, since it is necessary that the functions be continuous in the B.Z. The symmetry along the axis should be similar to, but of lower order than that at the center. The compatibility relations are somewhat complicated to obtain but we can verify for example at Γ the quantity in table-9 is 1 and then using it is seen that:

The energy bands of Te Note:- 1) The crystal field removes the degeneracy at the intersection of the and (200) curve for the point A. The higher energy curves for NFE are sketched based on the curves for FE and the use of the compatibility relations. 2) In this case, since and,so that the curves joining a and can only belong to.

Concluding Remarks We saw group theory does not give quantitative answers but it merely assisted in the band structure calculation in the following 2 ways: 1) To simplify the evaluation of secular determinants, 2) To determine the degeneracies of energy bands. However, the group theoretical framework can be extended(by taking into account dynamical symmetries) to give quantitative answers to dispersion relations, transfer matrices and energy bands. Ref: D.Kusnezov, arxiv:cond-mat/9907202v1

References o Allen Nussbaum, Solid State Physics,Vol.18,1966,p.165-272; Science Direct. o Group Theory in Physics,Vol.1 by J.F.Cornwell. Thanks to A. Sinha for useful discussions.