Stationary States in a Potential Well- H.C
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Accomplishments in Nanotechnology
U.S. Department of Commerce Carlos M. Gutierrez, Secretaiy Technology Administration Robert Cresanti, Under Secretaiy of Commerce for Technology National Institute ofStandards and Technolog}' William Jeffrey, Director Certain commercial entities, equipment, or materials may be identified in this document in order to describe an experimental procedure or concept adequately. Such identification does not imply recommendation or endorsement by the National Institute of Standards and Technology, nor does it imply that the materials or equipment used are necessarily the best available for the purpose. National Institute of Standards and Technology Special Publication 1052 Natl. Inst. Stand. Technol. Spec. Publ. 1052, 186 pages (August 2006) CODEN: NSPUE2 NIST Special Publication 1052 Accomplishments in Nanoteciinology Compiled and Edited by: Michael T. Postek, Assistant to the Director for Nanotechnology, Manufacturing Engineering Laboratory Joseph Kopanski, Program Office and David Wollman, Electronics and Electrical Engineering Laboratory U. S. Department of Commerce Technology Administration National Institute of Standards and Technology Gaithersburg, MD 20899 August 2006 National Institute of Standards and Teclinology • Technology Administration • U.S. Department of Commerce Acknowledgments Thanks go to the NIST technical staff for providing the information outlined on this report. Each of the investigators is identified with their contribution. Contact information can be obtained by going to: http ://www. nist.gov Acknowledged as well, -
Unit 1 Old Quantum Theory
UNIT 1 OLD QUANTUM THEORY Structure Introduction Objectives li;,:overy of Sub-atomic Particles Earlier Atom Models Light as clectromagnetic Wave Failures of Classical Physics Black Body Radiation '1 Heat Capacity Variation Photoelectric Effect Atomic Spectra Planck's Quantum Theory, Black Body ~diation. and Heat Capacity Variation Einstein's Theory of Photoelectric Effect Bohr Atom Model Calculation of Radius of Orbits Energy of an Electron in an Orbit Atomic Spectra and Bohr's Theory Critical Analysis of Bohr's Theory Refinements in the Atomic Spectra The61-y Summary Terminal Questions Answers 1.1 INTRODUCTION The ideas of classical mechanics developed by Galileo, Kepler and Newton, when applied to atomic and molecular systems were found to be inadequate. Need was felt for a theory to describe, correlate and predict the behaviour of the sub-atomic particles. The quantum theory, proposed by Max Planck and applied by Einstein and Bohr to explain different aspects of behaviour of matter, is an important milestone in the formulation of the modern concept of atom. In this unit, we will study how black body radiation, heat capacity variation, photoelectric effect and atomic spectra of hydrogen can be explained on the basis of theories proposed by Max Planck, Einstein and Bohr. They based their theories on the postulate that all interactions between matter and radiation occur in terms of definite packets of energy, known as quanta. Their ideas, when extended further, led to the evolution of wave mechanics, which shows the dual nature of matter -
Federico Capasso “Physics by Design: Engineering Our Way out of the Thz Gap” Peter H
6 IEEE TRANSACTIONS ON TERAHERTZ SCIENCE AND TECHNOLOGY, VOL. 3, NO. 1, JANUARY 2013 Terahertz Pioneer: Federico Capasso “Physics by Design: Engineering Our Way Out of the THz Gap” Peter H. Siegel, Fellow, IEEE EDERICO CAPASSO1credits his father, an economist F and business man, for nourishing his early interest in science, and his mother for making sure he stuck it out, despite some tough moments. However, he confesses his real attraction to science came from a well read children’s book—Our Friend the Atom [1], which he received at the age of 7, and recalls fondly to this day. I read it myself, but it did not do me nearly as much good as it seems to have done for Federico! Capasso grew up in Rome, Italy, and appropriately studied Latin and Greek in his pre-university days. He recalls that his father wisely insisted that he and his sister become fluent in English at an early age, noting that this would be a more im- portant opportunity builder in later years. In the 1950s and early 1960s, Capasso remembers that for his family of friends at least, physics was the king of sciences in Italy. There was a strong push into nuclear energy, and Italy had a revered first son in En- rico Fermi. When Capasso enrolled at University of Rome in FREDERICO CAPASSO 1969, it was with the intent of becoming a nuclear physicist. The first two years were extremely difficult. University of exams, lack of grade inflation and rigorous course load, had Rome had very high standards—there were at least three faculty Capasso rethinking his career choice after two years. -
Quantum Mechanics in One Dimension
Solved Problems on Quantum Mechanics in One Dimension Charles Asman, Adam Monahan and Malcolm McMillan Department of Physics and Astronomy University of British Columbia, Vancouver, British Columbia, Canada Fall 1999; revised 2011 by Malcolm McMillan Given here are solutions to 15 problems on Quantum Mechanics in one dimension. The solutions were used as a learning-tool for students in the introductory undergraduate course Physics 200 Relativity and Quanta given by Malcolm McMillan at UBC during the 1998 and 1999 Winter Sessions. The solutions were prepared in collaboration with Charles Asman and Adam Monaham who were graduate students in the Department of Physics at the time. The problems are from Chapter 5 Quantum Mechanics in One Dimension of the course text Modern Physics by Raymond A. Serway, Clement J. Moses and Curt A. Moyer, Saunders College Publishing, 2nd ed., (1997). Planck's Constant and the Speed of Light. When solving numerical problems in Quantum Mechanics it is useful to note that the product of Planck's constant h = 6:6261 × 10−34 J s (1) and the speed of light c = 2:9979 × 108 m s−1 (2) is hc = 1239:8 eV nm = 1239:8 keV pm = 1239:8 MeV fm (3) where eV = 1:6022 × 10−19 J (4) Also, ~c = 197:32 eV nm = 197:32 keV pm = 197:32 MeV fm (5) where ~ = h=2π. Wave Function for a Free Particle Problem 5.3, page 224 A free electron has wave function Ψ(x; t) = sin(kx − !t) (6) •Determine the electron's de Broglie wavelength, momentum, kinetic energy and speed when k = 50 nm−1. -
Class 2: Operators, Stationary States
Class 2: Operators, stationary states Operators In quantum mechanics much use is made of the concept of operators. The operator associated with position is the position vector r. As shown earlier the momentum operator is −iℏ ∇ . The operators operate on the wave function. The kinetic energy operator, T, is related to the momentum operator in the same way that kinetic energy and momentum are related in classical physics: p⋅ p (−iℏ ∇⋅−) ( i ℏ ∇ ) −ℏ2 ∇ 2 T = = = . (2.1) 2m 2 m 2 m The potential energy operator is V(r). In many classical systems, the Hamiltonian of the system is equal to the mechanical energy of the system. In the quantum analog of such systems, the mechanical energy operator is called the Hamiltonian operator, H, and for a single particle ℏ2 HTV= + =− ∇+2 V . (2.2) 2m The Schrödinger equation is then compactly written as ∂Ψ iℏ = H Ψ , (2.3) ∂t and has the formal solution iHt Ψ()r,t = exp − Ψ () r ,0. (2.4) ℏ Note that the order of performing operations is important. For example, consider the operators p⋅ r and r⋅ p . Applying the first to a wave function, we have (pr⋅) Ψ=−∇⋅iℏ( r Ψ=−) i ℏ( ∇⋅ rr) Ψ− i ℏ( ⋅∇Ψ=−) 3 i ℏ Ψ+( rp ⋅) Ψ (2.5) We see that the operators are not the same. Because the result depends on the order of performing the operations, the operator r and p are said to not commute. In general, the expectation value of an operator Q is Q=∫ Ψ∗ (r, tQ) Ψ ( r , td) 3 r . -
On a Classical Limit for Electronic Degrees of Freedom That Satisfies the Pauli Exclusion Principle
On a classical limit for electronic degrees of freedom that satisfies the Pauli exclusion principle R. D. Levine* The Fritz Haber Research Center for Molecular Dynamics, The Hebrew University, Jerusalem 91904, Israel; and Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095 Contributed by R. D. Levine, December 10, 1999 Fermions need to satisfy the Pauli exclusion principle: no two can taken into account, this starting point is not necessarily a be in the same state. This restriction is most compactly expressed limitation. There are at least as many orbitals (or, strictly in a second quantization formalism by the requirement that the speaking, spin orbitals) as there are electrons, but there can creation and annihilation operators of the electrons satisfy anti- easily be more orbitals than electrons. There are usually more commutation relations. The usual classical limit of quantum me- states than orbitals, and in the model of quantum dots that chanics corresponds to creation and annihilation operators that motivated this work, the number of spin orbitals is twice the satisfy commutation relations, as for a harmonic oscillator. We number of sites. For the example of 19 sites, there are 38 discuss a simple classical limit for Fermions. This limit is shown to spin-orbitals vs. 2,821,056,160 doublet states. correspond to an anharmonic oscillator, with just one bound The point of the formalism is that it ensures that the Pauli excited state. The vibrational quantum number of this anharmonic exclusion principle is satisfied, namely that no more than one oscillator, which is therefore limited to the range 0 to 1, is the electron occupies any given spin-orbital. -
Electronic Supplementary Information: Low Ensemble Disorder in Quantum Well Tube Nanowires
Electronic Supplementary Material (ESI) for Nanoscale. This journal is © The Royal Society of Chemistry 2015 Electronic Supplementary Information: Low Ensemble Disorder in Quantum Well Tube Nanowires Christopher L. Davies,∗a Patrick Parkinson,b Nian Jiang,c Jessica L. Boland,a Sonia Conesa-Boj,a H. Hoe Tan,c Chennupati Jagadish,c Laura M. Herz,a and Michael B. Johnston.a‡ (a) 3.950 nm (b) GaAs-QW 2.026 nm 2.181 nm 4.0 nm 3.962 nm 50 nm 20 nm GaAs-core Fig. S1 TEM image of top of B50 sample Fig. S2 TEM image of bottom of B50 sample S1 TEM Figure S1(a) corresponds to a low magnification bright field TEM image of a representative cross-section of the sample B50. The thickness of the GaAs QW has been measured in different regions. S2 1D Finite Square Well Model The variations in thickness are found to be around 4 nm and 2 For a semiconductor the Fermi-Dirac distribution for electrons in nm in the edges and in the facets, respectively, confirming the the conduction band and holes in the valence band is given by, disorder in the GaAs QW. In the HR-TEM image performed in 1 one of the edges of the nanowire cross section, figure S1(b), the f = ; (1) e,h exp((E − Ec,v) ) + 1 variation in the QW thickness (marked by white dashed lines) f b between the edge and the facets is clearly visible. c,v where b = 1=kBT, T is the electron temperature and Ef is the Figures S2 and S3 are additional TEM images of sample B50 Fermi energies of the electrons and holes. -
Wave Mechanics (PDF)
WAVE MECHANICS B. Zwiebach September 13, 2013 Contents 1 The Schr¨odinger equation 1 2 Stationary Solutions 4 3 Properties of energy eigenstates in one dimension 10 4 The nature of the spectrum 12 5 Variational Principle 18 6 Position and momentum 22 1 The Schr¨odinger equation In classical mechanics the motion of a particle is usually described using the time-dependent position ix(t) as the dynamical variable. In wave mechanics the dynamical variable is a wave- function. This wavefunction depends on position and on time and it is a complex number – it belongs to the complex numbers C (we denote the real numbers by R). When all three dimensions of space are relevant we write the wavefunction as Ψ(ix, t) C . (1.1) ∈ When only one spatial dimension is relevant we write it as Ψ(x, t) C. The wavefunction ∈ satisfies the Schr¨odinger equation. For one-dimensional space we write ∂Ψ 2 ∂2 i (x, t) = + V (x, t) Ψ(x, t) . (1.2) ∂t −2m ∂x2 This is the equation for a (non-relativistic) particle of mass m moving along the x axis while acted by the potential V (x, t) R. It is clear from this equation that the wavefunction must ∈ be complex: if it were real, the right-hand side of (1.2) would be real while the left-hand side would be imaginary, due to the explicit factor of i. Let us make two important remarks: 1 1. The Schr¨odinger equation is a first order differential equation in time. This means that if we prescribe the wavefunction Ψ(x, t0) for all of space at an arbitrary initial time t0, the wavefunction is determined for all times. -
Optical Pumping: a Possible Approach Towards a Sige Quantum Cascade Laser
Institut de Physique de l’ Universit´ede Neuchˆatel Optical Pumping: A Possible Approach towards a SiGe Quantum Cascade Laser E3 40 30 E2 E1 20 10 Lasing Signal (meV) 0 210 215 220 Energy (meV) THESE pr´esent´ee`ala Facult´edes Sciences de l’Universit´ede Neuchˆatel pour obtenir le grade de docteur `essciences par Maxi Scheinert Soutenue le 8 octobre 2007 En pr´esence du directeur de th`ese Prof. J´erˆome Faist et des rapporteurs Prof. Detlev Gr¨utzmacher , Prof. Peter Hamm, Prof. Philipp Aebi, Dr. Hans Sigg and Dr. Soichiro Tsujino Keywords • Semiconductor heterostructures • Intersubband Transitions • Quantum cascade laser • Si - SiGe • Optical pumping Mots-Cl´es • H´et´erostructures semiconductrices • Transitions intersousbande • Laser `acascade quantique • Si - SiGe • Pompage optique i Abstract Since the first Quantum Cascade Laser (QCL) was realized in 1994 in the AlInAs/InGaAs material system, it has attracted a wide interest as infrared light source. Main applications can be found in spectroscopy for gas-sensing, in the data transmission and telecommuni- cation as free space optical data link as well as for infrared monitoring. This type of light source differs in fundamental ways from semiconductor diode laser, because the radiative transition is based on intersubband transitions which take place between confined states in quantum wells. As the lasing transition is independent from the nature of the band gap, it opens the possibility to a tuneable, infrared light source based on silicon and silicon compatible materials such as germanium. As silicon is the material of choice for electronic components, a SiGe based QCL would allow to extend the functionality of silicon into optoelectronics. -
The Time Evolution of a Wave Function
The Time Evolution of a Wave Function ² A \system" refers to an electron in a potential energy well, e.g., an electron in a one-dimensional in¯nite square well. The system is speci¯ed by a given Hamiltonian. ² Assume all systems are isolated. ² Assume all systems have a time-independent Hamiltonian operator H^ . ² TISE and TDSE are abbreviations for the time-independent SchrÄodingerequation and the time- dependent SchrÄodingerequation, respectively. P ² The symbol in all questions denotes a sum over a complete set of states. PART A ² Information for questions (I)-(VI) In the following questions, an electron is in a one-dimensional in¯nite square well of width L. (The q 2 n2¼2¹h2 stationary states are Ãn(x) = L sin(n¼x=L), and the allowed energies are En = 2mL2 , where n = 1; 2; 3:::) p (I) Suppose the wave function for an electron at time t = 0 is given by Ã(x; 0) = 2=L sin(5¼x=L). Which one of the following is the wave function at time t? q 2 (a) Ã(x; t) = sin(5¼x=L) cos(E5t=¹h) qL 2 ¡iE5t=¹h (b) Ã(x; t) = L sin(5¼x=L) e (c) Both (a) and (b) above are appropriate ways to write the wave function. (d) None of the above. q 2 (II) The wave function for an electron at time t = 0 is given by Ã(x; 0) = L sin(5¼x=L). Which one of the following is true about the probability density, jÃ(x; t)j2, after time t? 2 2 2 2 (a) jÃ(x; t)j = L sin (5¼x=L) cos (E5t=¹h). -
Optical Physics of Quantum Wells
Optical Physics of Quantum Wells David A. B. Miller Rm. 4B-401, AT&T Bell Laboratories Holmdel, NJ07733-3030 USA 1 Introduction Quantum wells are thin layered semiconductor structures in which we can observe and control many quantum mechanical effects. They derive most of their special properties from the quantum confinement of charge carriers (electrons and "holes") in thin layers (e.g 40 atomic layers thick) of one semiconductor "well" material sandwiched between other semiconductor "barrier" layers. They can be made to a high degree of precision by modern epitaxial crystal growth techniques. Many of the physical effects in quantum well structures can be seen at room temperature and can be exploited in real devices. From a scientific point of view, they are also an interesting "laboratory" in which we can explore various quantum mechanical effects, many of which cannot easily be investigated in the usual laboratory setting. For example, we can work with "excitons" as a close quantum mechanical analog for atoms, confining them in distances smaller than their natural size, and applying effectively gigantic electric fields to them, both classes of experiments that are difficult to perform on atoms themselves. We can also carefully tailor "coupled" quantum wells to show quantum mechanical beating phenomena that we can measure and control to a degree that is difficult with molecules. In this article, we will introduce quantum wells, and will concentrate on some of the physical effects that are seen in optical experiments. Quantum wells also have many interesting properties for electrical transport, though we will not discuss those here. -
Schrödinger Equation: (Time Independent) Hψ = Eψ This Is a Differential Eigenvalue Equation
Physics and Material Science of Semiconductor Nanostructures PHYS 570P Prof. Oana Malis Email: [email protected] Lecture 9 Review of quantum mechanics, statistical physics, and solid state Band structure of materials Semiconductor band structure Semiconductor nanostructures Ref. Davies Chapter 1 Quantum Mechanics (QM) • The Schrödinger Equation: (time independent) Hψ = Eψ This is a differential eigenvalue equation. H Hamiltonian operator for the system (energy operator) E Energy eigenvalue, ψ wavefunction Particles are QM waves! |ψ|2 probability density; ψ is a function of ALL coordinates of ALL particles in the problem! One Page Elementary Quantum Mechanics & Solid State Physics Review • Quantum Mechanics of a Free Electron: 2 – The energies are continuous: E = (k) /(2mo) (1d, 2d, or 3d) – The wavefunctions are traveling waves: ikx ikr ψk(x) = A e (1d) ψk(r) = A e (2d or 3d) • Solid State Physics: Quantum Mechanics of an Electron in a Periodic Potential in an infinite crystal : – The energy bands are (approximately) continuous: E= Enk – At the bottom of the conduction band or the top of the valence band, in the effective mass approximation, the bands can be written: 2 Enk (k) /(2m*) – The wavefunctions are Bloch Functions = traveling waves: ikr Ψnk(r) = e unk(r); unk(r) = unk(r+R) QM Review: The 1d (infinite) Potential Well (“particle in a box”) In all QM texts!! Consider the case of a particle in a 1-D potential well, with width L e infinite barriers V(x) = 0 for 0 x L V(x) = for x<0, x>L Schrödinger equation Inside the well