* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download INTRODUCTION TO QUANTUM MECHANICS I I mention in class
Atomic orbital wikipedia , lookup
Measurement in quantum mechanics wikipedia , lookup
Ferromagnetism wikipedia , lookup
Coherent states wikipedia , lookup
EPR paradox wikipedia , lookup
Atomic theory wikipedia , lookup
History of quantum field theory wikipedia , lookup
Aharonov–Bohm effect wikipedia , lookup
Hidden variable theory wikipedia , lookup
X-ray photoelectron spectroscopy wikipedia , lookup
Renormalization group wikipedia , lookup
Probability amplitude wikipedia , lookup
Electron configuration wikipedia , lookup
Tight binding wikipedia , lookup
Wave–particle duality wikipedia , lookup
Matter wave wikipedia , lookup
Renormalization wikipedia , lookup
Scalar field theory wikipedia , lookup
Path integral formulation wikipedia , lookup
Quantum state wikipedia , lookup
Perturbation theory (quantum mechanics) wikipedia , lookup
Symmetry in quantum mechanics wikipedia , lookup
Quantum electrodynamics wikipedia , lookup
Particle in a box wikipedia , lookup
Electron scattering wikipedia , lookup
Relativistic quantum mechanics wikipedia , lookup
Hydrogen atom wikipedia , lookup
Molecular Hamiltonian wikipedia , lookup
Theoretical and experimental justification for the Schrödinger equation wikipedia , lookup
INTRODUCTION TO QUANTUM MECHANICS I PROBLEM SET 4 due October 4th, before class I. DEGENERACY IN ONE DIMENSION, TUNNELING AND ALL THAT I mention in class how the energy eigenvalues in one dimension are never degenerate. That may seem counterintuitive. In fact, consider two identical potential wells separated by a vast distance. One could imagine that a wave function concentrated around one well would be degenerate in energy with an identical function concentrated around the other well. To understand this better, let us consider two attractive δ function potentials separated by a distance L: L L V (x) = −λ δ(x − ) + δ(x + ) , (1) 2 2 with λ > 0. 1. Find the bound states and their energies. 2. Consider the limit L → ∞. How can we (approximately) write the eigenstates in terms of linear combinations of the eigenstates of each well separately. Is the intuition described below (namely, that the corrected eigenstates of the double well are essentially the eigenstates of the single well) correct? 3. We can abstract the double well potential into a more general situation. Imagine that initially we have a hamiltonian that is degenerate E0 0 Ĥ0 = . (2) 0 E0 These two degenerate states could correspond to the ground states of two identical single wells. Suppose now we turn a very small interaction (maybe due to tunneling between the two wells) 0 T . (3) ĤI = T 0 Show that the eigenvalues of Ĥ = Ĥ0 + ĤI are no longer degenerate. Find also the eigenstates of Ĥ. II. HOW THE PREVIOUS PROBLEM EXPLAINS COVALENT BINDING OR “CHEMISTRY AS A FOOTNOTE OF QUANTUM MECHANICS” Let us make a crude model of a + H2 molecule (that is two protons and one electron). Imagine the protons are held at fixed positions. The electron can be bound to each one of the protons, so we approximate the Hilbert space by a two-dimensional space. When the electron is bound to one proton it has an energy E0 < 0. But there is always a small probability for it to tunnel through the other proton (with a probability amplitude T ) so the full hamiltonian (well, the crude approximation to it in the two-dimensional Hilbert space) is like the two-dimensional Ĥ above. Using the result above you now what the energy of the electron will be. 1. Assuming that T should be larger when the protons are closer, make a qualitative drawing of the two energy levels as a function of the distance between the protons. 2. In addition to the energy of the electron, there is a repulsive Coulomb energy between the protons. Make a qualitative plot of the sum of Coulomb plus electron energy. The minimum is the preferred distance between the two protons, that is, the size of the + H2 molecule. That is the quantum mechanical explanation of the fact that a “shared electron” binds atoms together, that always baffled me in high school. A better description of covalent binding that I can give here but along similar lines is given in “Atomic Physics” by Max Born. 2 III. PARTICLE IN A MAGNETIC FIELD ~ Its lagrangian is given by Consider a charged particle moving in three dimensions subject to a magnetic field B. L= m~x˙ 2 ~ + q~x˙ .A, 2 (4) ~ = ∇ × A. ~ The goal of this problem is to apply the canonical quantization method and find a formulation of with B the quantum theory of a charged, spinless particle moving on an external magnetic field. 1. Verify that the equations of motion following this lagrangian yield Newton+Lorentz force. 2. Find the (classical) momentum canonically related to the position ~x. 3. What is the quantum mechanical operator associated with the canonical momentum above ? 4. What is the quantum mechanical operator for the velocity ~x˙ ? 5. Find the classical hamiltonian H. 6. find the quantum hamiltonian Ĥ. 7. Write the quantum hamiltonian operator in the position eigenbasis. IV. SQUARE WELL Does the potential V (x) = −V0 , −L/2 < x < L/2 0, x > L/2 or x < −L/2 (5) have a bound state for any l and V0 ? What is the binding energy? If you have any conceptual problem solving this problem stop everything and solve all problems in Griffiths now. V. ONE DIMENSIONAL ATTRACTIVE POTENTIALS HAVE A BOUND STATE 1. Show that if two hamiltonians differ only in their potential and if V1 (x) < V2 (x) for all x, then the ground state energy of Ĥ1 is smaller than the ground state energy of Ĥ2 . 2. Use this result and the square well problem to show that any attractive potential in 1D has at least one bound state. This result is valid only in one dimension! VI. A FIRST LOOK AT THE VARIATIONAL PRINCIPLE Show that the minimum of the functional # " 2 Z ∞ ~2 dψ(x) 2 + V (x)|ψ(x)| [ψ] = dx 2m dx −∞ (6) under the constraint Z ∞ dx |ψ(x)|2 = 1, (7) −∞ is given by the energy eigenstates. Then show that the minimum of the functional is given by the ground state. Hint: you may want to brush up on the concept of Lagrange multipliers and the Euler-Lagrange equations of calculus of variations.