The Orbital Magnetic Moment in Terms of Bohr Magneton in the Vector Form Is
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Magnetism, Magnetic Properties, Magnetochemistry
Magnetism, Magnetic Properties, Magnetochemistry 1 Magnetism All matter is electronic Positive/negative charges - bound by Coulombic forces Result of electric field E between charges, electric dipole Electric and magnetic fields = the electromagnetic interaction (Oersted, Maxwell) Electric field = electric +/ charges, electric dipole Magnetic field ??No source?? No magnetic charges, N-S No magnetic monopole Magnetic field = motion of electric charges (electric current, atomic motions) Magnetic dipole – magnetic moment = i A [A m2] 2 Electromagnetic Fields 3 Magnetism Magnetic field = motion of electric charges • Macro - electric current • Micro - spin + orbital momentum Ampère 1822 Poisson model Magnetic dipole – magnetic (dipole) moment [A m2] i A 4 Ampere model Magnetism Microscopic explanation of source of magnetism = Fundamental quantum magnets Unpaired electrons = spins (Bohr 1913) Atomic building blocks (protons, neutrons and electrons = fermions) possess an intrinsic magnetic moment Relativistic quantum theory (P. Dirac 1928) SPIN (quantum property ~ rotation of charged particles) Spin (½ for all fermions) gives rise to a magnetic moment 5 Atomic Motions of Electric Charges The origins for the magnetic moment of a free atom Motions of Electric Charges: 1) The spins of the electrons S. Unpaired spins give a paramagnetic contribution. Paired spins give a diamagnetic contribution. 2) The orbital angular momentum L of the electrons about the nucleus, degenerate orbitals, paramagnetic contribution. The change in the orbital moment -
Lecture #4, Matter/Energy Interactions, Emissions Spectra, Quantum Numbers
Welcome to 3.091 Lecture 4 September 16, 2009 Matter/Energy Interactions: Atomic Spectra 3.091 Periodic Table Quiz 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 Name Grade /10 Image by MIT OpenCourseWare. Rutherford-Geiger-Marsden experiment Image by MIT OpenCourseWare. Bohr Postulates for the Hydrogen Atom 1. Rutherford atom is correct 2. Classical EM theory not applicable to orbiting e- 3. Newtonian mechanics applicable to orbiting e- 4. Eelectron = Ekinetic + Epotential 5. e- energy quantized through its angular momentum: L = mvr = nh/2π, n = 1, 2, 3,… 6. Planck-Einstein relation applies to e- transitions: ΔE = Ef - Ei = hν = hc/λ c = νλ _ _ 24 1 18 Bohr magneton µΒ = eh/2me 9.274 015 4(31) X 10 J T 0.34 _ _ 27 1 19 Nuclear magneton µΝ = eh/2mp 5.050 786 6(17) X 10 J T 0.34 _ 2 3 20 Fine structure constant α = µ0ce /2h 7.297 353 08(33) X 10 0.045 21 Inverse fine structure constant 1/α 137.035 989 5(61) 0.045 _ 2 1 22 Rydberg constant R¥ = mecα /2h 10 973 731.534(13) m 0.0012 23 Rydberg constant in eV R¥ hc/{e} 13.605 698 1(40) eV 0.30 _ 10 24 Bohr radius a0 = a/4πR¥ 0.529 177 249(24) X 10 m 0.045 _ _ 4 2 1 25 Quantum of circulation h/2me 3.636 948 07(33) X 10 m s 0.089 _ 11 1 26 Electron specific charge -e/me -1.758 819 62(53) X 10 C kg 0.30 _ 12 27 Electron Compton wavelength λC = h/mec 2.426 310 58(22) X 10 m 0.089 _ 2 15 28 Electron classical radius re = α a0 2.817 940 92(38) X 10 m 0.13 _ _ 26 1 29 Electron magnetic moment` µe 928.477 01(31) X 10 J T 0.34 _ _ 3 30 Electron mag. -
1. Physical Constants 1 1
1. Physical constants 1 1. PHYSICAL CONSTANTS Table 1.1. Reviewed 1998 by B.N. Taylor (NIST). Based mainly on the “1986 Adjustment of the Fundamental Physical Constants” by E.R. Cohen and B.N. Taylor, Rev. Mod. Phys. 59, 1121 (1987). The last group of constants (beginning with the Fermi coupling constant) comes from the Particle Data Group. The figures in parentheses after the values give the 1-standard- deviation uncertainties in the last digits; the corresponding uncertainties in parts per million (ppm) are given in the last column. This set of constants (aside from the last group) is recommended for international use by CODATA (the Committee on Data for Science and Technology). Since the 1986 adjustment, new experiments have yielded improved values for a number of constants, including the Rydberg constant R∞, the Planck constant h, the fine- structure constant α, and the molar gas constant R,and hence also for constants directly derived from these, such as the Boltzmann constant k and Stefan-Boltzmann constant σ. The new results and their impact on the 1986 recommended values are discussed extensively in “Recommended Values of the Fundamental Physical Constants: A Status Report,” B.N. Taylor and E.R. Cohen, J. Res. Natl. Inst. Stand. Technol. 95, 497 (1990); see also E.R. Cohen and B.N. Taylor, “The Fundamental Physical Constants,” Phys. Today, August 1997 Part 2, BG7. In general, the new results give uncertainties for the affected constants that are 5 to 7 times smaller than the 1986 uncertainties, but the changes in the values themselves are smaller than twice the 1986 uncertainties. -
Magnetism in Transition Metal Complexes
Magnetism for Chemists I. Introduction to Magnetism II. Survey of Magnetic Behavior III. Van Vleck’s Equation III. Applications A. Complexed ions and SOC B. Inter-Atomic Magnetic “Exchange” Interactions © 2012, K.S. Suslick Magnetism Intro 1. Magnetic properties depend on # of unpaired e- and how they interact with one another. 2. Magnetic susceptibility measures ease of alignment of electron spins in an external magnetic field . 3. Magnetic response of e- to an external magnetic field ~ 1000 times that of even the most magnetic nuclei. 4. Best definition of a magnet: a solid in which more electrons point in one direction than in any other direction © 2012, K.S. Suslick 1 Uses of Magnetic Susceptibility 1. Determine # of unpaired e- 2. Magnitude of Spin-Orbit Coupling. 3. Thermal populations of low lying excited states (e.g., spin-crossover complexes). 4. Intra- and Inter- Molecular magnetic exchange interactions. © 2012, K.S. Suslick Response to a Magnetic Field • For a given Hexternal, the magnetic field in the material is B B = Magnetic Induction (tesla) inside the material current I • Magnetic susceptibility, (dimensionless) B > 0 measures the vacuum = 0 material response < 0 relative to a vacuum. H © 2012, K.S. Suslick 2 Magnetic field definitions B – magnetic induction Two quantities H – magnetic intensity describing a magnetic field (Système Internationale, SI) In vacuum: B = µ0H -7 -2 µ0 = 4π · 10 N A - the permeability of free space (the permeability constant) B = H (cgs: centimeter, gram, second) © 2012, K.S. Suslick Magnetism: Definitions The magnetic field inside a substance differs from the free- space value of the applied field: → → → H = H0 + ∆H inside sample applied field shielding/deshielding due to induced internal field Usually, this equation is rewritten as (physicists use B for H): → → → B = H0 + 4 π M magnetic induction magnetization (mag. -
31295015501306.Pdf (1.378Mb)
A STUDY OF TK3 MGN3TIC PROPERTIES OF FERROCYAKTDij^S AND FERRICYANIDES by JACK ED7ARD RANDORFF, B. S. A THESIS IN PHYSICS Submitted to the Graduate Faculty of Texas Technological College in Partial Fulfillment of the Requirements for the Degree of MASTER OF SCISIICE Approved Accented June, 1967 f^(A^fjin Cop. a ACKNO/JLEDGS-IENTS I am deeply appreciative of Dr. Billy J. I4arshall for his direction of this thesis; to the Robert A. Welch Foundation of Texas for financial support given to this project; to Dr. V/, 0, Milligan, research director of the forementioned Foundatior^ for the helpful and stimulating discussion with regard to this work and to his research group at Baylor University for the preparation of samples; and to the U. S. Department of Health, Education and V'elfrro for tho presentation of an N,D,E,A. Title IV Fellowship as financial support to pursue this study. ii TABLE OF COirrSxNTS ACKNO'WLEDG&IEOTS ii TABLE OF CONTENTS iii LIST OF TABLES iv LIST OF FIGURES v I, INTRODUCnON 1 II. EXPERIMEOTAL TECHMIQUE 3 Sample Preparation 3 Apparatus 3 Temperature Control and Detection 5 Calibrations and Corrections 6 Set-up Procedure 8 III, RESULTS Aim Discussion l6 IV. FUTURE WORK 33 LIST OF REFERENCES 34 APPENDIX I 35 APPENDIX II 42 APPENDIX III 43 iii LIST OF TABLES Table 1, The values of susceptibility and temperature.,, 19 Table 2, Effective number of Bohr Diagnetons per atom or per molecule, 20 iv LIST OF FIGURES Figure 1, Apparatus Assembly. 9 Figure lA. Internal view of Cahn RM Automatic Electrobalance, 10 Figure 2. -
Lecture 41 (Spatial Quantization & Electron Spin)
Lecture 41 (Spatial Quantization & Electron Spin) Physics 2310-01 Spring 2020 Douglas Fields Quantum States • Breaking Symmetry • Remember that degeneracies were the reflection of symmetries. What if we break some of the symmetry by introducing something that distinguishes one direction from another? • One way to do that is to introduce a magnetic field. • To investigate what happens when we do this, we will briefly use the Bohr model in order to calculate the effect of a magnetic field on an orbiting electron. • In the Bohr model, we can think of an electron causing a current loop. • This current loop causes a magnetic moment: • We can calculate the current and the area from a classical picture of the electron in a circular orbit: • Where the minus sign just reflects the fact that it is negatively charged, so that the current is in the opposite direction of the electron’s motion. Bohr Magneton • Now, we use the classical definition of angular momentum to put the magnetic moment in terms of the orbital angular momentum: • And now use the Bohr quantization for orbital angular momentum: • Which is called the Bohr magneton, the magnetic moment of a n=1 electron in Bohr’s model. Back to Breaking Symmetry • It turns out that the magnetic moment of an electron in the Schrödinger model has the same form as Bohr’s model: • Now, what happens again when we break a symmetry, say by adding an external magnetic field? Back to Breaking Symmetry • Thanks, yes, we should lose degeneracies. • But how and why? • Well, a magnetic moment in a magnetic field feels a torque: • And thus, it can have a potential energy: • Or, in our case: Zeeman Effect • This potential energy breaks the degeneracy and splits the degenerate energy levels into distinct energies. -
Chapter 1 MAGNETIC NEUTRON SCATTERING
Chapter 1 MAGNETIC NEUTRON SCATTERING. And Recent Developments in the Triple Axis Spectroscopy Igor A . Zaliznyak'" and Seung-Hun Lee(2) (')Department of Physics. Brookhaven National Laboratory. Upton. New York 11973-5000 (')National Institute of Standards and Technology. Gaithersburg. Maryland 20899 1. Introduction..................................................................................... 2 2 . Neutron interaction with matter and scattering cross-section ......... 6 2.1 Basic scattering theory and differential cross-section................. 7 2.2 Neutron interactions and scattering lengths ................................ 9 2.2.1 Nuclear scattering length .................................................. 10 2.2.2 Magnetic scattering length ................................................ 11 2.3 Factorization of the magnetic scattering length and the magnetic form factors ............................................................................................... 16 2.3.1 Magnetic form factors for Hund's ions: vector formalism19 2.3.2 Evaluating the form factors and dipole approximation..... 22 2.3.3 One-electron spin form factor beyond dipole approximation; anisotropic form factors for 3d electrons..................... 27 3 . Magnetic scattering by a crystal ................................................... 31 3.1 Elastic and quasi-elastic magnetic scattering............................ 34 3.2 Dynamical correlation function and dynamical magnetic susceptibility ............................................................................................ -
I Magnetism in Nature
We begin by answering the first question: the I magnetic moment creates magnetic field lines (to which B is parallel) which resemble in shape of an Magnetism in apple’s core: Nature Lecture notes by Assaf Tal 1. Basic Spin Physics 1.1 Magnetism Before talking about magnetic resonance, we need to recount a few basic facts about magnetism. Mathematically, if we have a point magnetic Electromagnetism (EM) is the field of study moment m at the origin, and if r is a vector that deals with magnetic (B) and electric (E) fields, pointing from the origin to the point of and their interactions with matter. The basic entity observation, then: that creates electric fields is the electric charge. For example, the electron has a charge, q, and it creates 0 3m rˆ rˆ m q 1 B r 3 an electric field about it, E 2 rˆ , where r 40 r 4 r is a vector extending from the electron to the point of observation. The electric field, in turn, can act The magnitude of the generated magnetic field B on another electron or charged particle by applying is proportional to the size of the magnetic charge. a force F=qE. The direction of the magnetic moment determines the direction of the field lines. For example, if we tilt the moment, we tilt the lines with it: E E q q F Left: a (stationary) electric charge q will create a radial electric field about it. Right: a charge q in a constant electric field will experience a force F=qE. -
Magnetic Susceptibility Measurements of Transition Metal Containing Compounds
Magnetic susceptibility measurements of transition metal containing compounds Introduction: Measurements of magnetic properties have been used to characterize a wide range of systems from oxygen, metallic alloys, solid state materials, and coordination complexes containing metals. Most organic and main group element compounds have all the electrons paired and these are diamagnetic molecules with very small magnetic moments. All of the transition metals have at least one oxidation state with an incomplete d subshell. Magnetic measurements, particularly for the first row transition elements, give information about the number of unpaired electrons. The number of unpaired electrons provides information about the oxidation state and electron configuration. The determination of the magnetic properties of the second and third row transition elements is more complex. The magnetic moment is calculated from the magnetic susceptibility, since the magnetic moment is not measured directly. There are several ways to express the degree to which a material acquires a magnetic moment in a field. The magnetic susceptibility per unit volume is defined by: I H where I is the intensity of the magnetization induced in the sample by the external magnetic field, H. The extent of the magnetic induction (I) depends on the sample. The induction may be visualized as an alignment of dipoles and/or by the formation of charge polarization in the sample. H is the strength of the external magnetic field in units of oersteds (Oe). The κ is unitless. Generally, it is more convenient to use mass units, therefore the mass or gram susceptibility is defined as: g d where d is the density of the solid. -
Magnetochemistry
Magnetochemistry (12.7.06) H.J. Deiseroth, SS 2006 Magnetochemistry The magnetic moment of a single atom (µ) (µ is a vector !) μ µ μ = i F [Am2], circular current i, aerea F F -27 2 μB = eh/4πme = 0,9274 10 Am (h: Planck constant, me: electron mass) μB: „Bohr magneton“ (smallest quantity of a magnetic moment) → for one unpaired electron in an atom („spin only“): s μ = 1,73 μB Magnetochemistry → The magnetic moment of an atom has two components a spin component („spin moment“) and an orbital component („orbital moment“). →Frequently the orbital moment is supressed („spin-only- magnetism“, e.g. coordination compounds of 3d elements) Magnetisation M and susceptibility χ M = (∑ μ)/V ∑ μ: sum of all magnetic moments μ in a given volume V, dimension: [Am2/m3 = A/m] The actual magnetization of a given sample is composed of the „intrinsic“ magnetization (susceptibility χ) and an external field H: M = H χ (χ: suszeptibility) Magnetochemistry There are three types of susceptibilities: χV: dimensionless (volume susceptibility) 3 χg:[cm/g] (gramm susceptibility) 3 χm: [cm /mol] (molar susceptibility) !!!!! χm is used normally in chemistry !!!! Frequently: χ = f(H) → complications !! Magnetochemistry Diamagnetism - external field is weakened - atoms/ions/molecules with closed shells -4 -2 3 -10 < χm < -10 cm /mol (negative sign) Paramagnetism (van Vleck) - external field is strengthened - atoms/ions/molecules with open shells/unpaired electrons -4 -1 3 +10 < χm < 10 cm /mol → diamagnetism (core electrons) + paramagnetism (valence electrons) Magnetism -
A Supplementary Discussion on Bohr Magneton Magnetic Fields Arise from Moving Electric Charges. a Charge Q with Velocity V Gives
A Supplementary Discussion on Bohr Magneton Magnetic fields arise from moving electric charges. A charge q with velocity v gives rise to a magnetic field B, following SI convention in units of Tesla, µ qv × r B = 0 , 4π r3 −7 −2 2 where µ0 is the vacuum permeability and is defined as 4π × 10 NC s . Now consider a magnetic dipole moment as a charge q moving in a circle with radius r with speed v. The current is the charge flow per unit time. Since the circumference of the circle is 2πr, and the time for one revolution is 2πr/v, one has the current as I = qv/2πr. The magnitude of the dipole moment is |µ| = I · (area) = (qv/2πr)πr2 = qrp/2m, where p is the linear momentum. Since the radial vector r is perpendicular to p, we have qr × p q µ = = L, 2m 2m where L is the angular momentum. The magnitude of the orbital magnetic momentum of an electron with orbital-angular- momentum quantum l is e¯h 1/2 1/2 µ = [l(l + 1)] = µB[l(l + 1)] . 2me Here, µB is a constant called Bohr magneton, and is equal to −19 −34 e¯h (1.6 × 10 C) × (6.626 × 10 J · s/2π) −24 µB = = −31 = 9.274 × 10 J/T, 2me 2 × 9.11 × 10 kg where T is magnetic field, Tesla. Now consider applying an external magnetic field B along the z-axis. The energy of interaction between this magnetic field and the magnetic dipole moment is e µB EB = −µ · B = Lz · B = BLz. -
Magnetic Moment
Magnetic moment Bohr magneton Magnetic moment gyromagnetic ratio (g factor) determined by details of charge distribution (elementary particle e.g. electron) (QED corrections for electron) 7-31. Assuming the electron to be a classical particle, a sphere of radius 10-15 m and a uniform mass density, use the magnitude of the spin angular momentum | S | = [s (s+1)]1/2 ħ=(3/4)1/2 ħ to compute the speed of rotation at the electron’s equator. How does your result compare with the speed of light? Magnetic moment Stern-Gerlach experiment Inhomogeneous magnetic field Stern-Gerlach experiment Inhomogeneous magnetic field Stern-Gerlach experiment Inhomogeneous magnetic field Classical picture – continuum of possible orientations Quantum mechanics– 2l +1 deflections ? Stern-Gerlach experiment Total Angular Momentum total angular momentum or If J1 is one angular momentum (orbital, spin, or a combination) and J2 is another, the resulting total angular momentum J = J1 + J2 has the value [ j ( j + 1)]1/2 ħ for its magnitude, where j can be any of the values j1 + j2, j1 + j2 - 1, . , | j1 - j2 | 7-34. (a) The angular momentum of the yttrium atom in the ground state is characterized by the quantum number j = 3/2. How many lines would you expect to see if you could do a Stern-Gerlach experiment with yttrium atoms? (b) How many lines would you expect to see if the beam consisted of atoms with zero spin, but l= 1? a) b) 7-37. A hydrogen atom is in the 3d state (n = 3, l = 2). (a) What are the possible values of j? (b) What are the possible values of the magnitude of the total angular momentum? (c) What are the possible z components of the total angular momentum? a) b) c) Spectroscopic Notation Single electron s p d f g h l 0 1 2 3 4 5 K L M N O n 1 2 3 4 5 Atomic state total spin total orbital angular momentum n total angular momentum Hydrogen ground state Identical Particles in Quantum Mechanics Non-interacting particles e.g.