7.1 Application of the Schr ö dinger Equation to the Hydrogen Atom

1. CHAPTER 7The Hydrogen Atom • 7.1 Application of the Schrödinger Equation to the Hydrogen Atom • 7.2 Solution of the Schrödinger Equation for Hydrogen • 7.3 Quantum Numbers • 7.4 Magnetic Effects on Atomic Spectra–The Zeeman Effect • 7.5 Intrinsic Spin • 7.6 Energy Levels and Electron Probabilities Werner Heisenberg (1901-1976) The atom of modern physics can be symbolized only through a partial differential equation in an abstract space of many dimensions. All its qualities are inferential; no material properties can be directly attributed to it. An understanding of the atomic world in that primary sensuous fashion…is impossible. - Werner Heisenberg

2. 7.1: Application of the Schrödinger Equation to the Hydrogen Atom The potential energy of the electron-proton system is electrostatic: Use the three-dimensional time-independent Schrödinger Equation. For Hydrogen-like atoms (He+ or Li++) Replace e2 with Ze2 (Z is the atomic number). Replace m with the reduced mass, m.

3. Spherical Coordinates Transform to spherical polar coordinates because of the radial symmetry. The potential (central force) V(r) depends on the distance r between the proton and electron.

4. The Schrödinger Equation in Spherical Coordinates Transformed into spherical coordinates, the Schrödinger equation becomes:

5. Separable Solution This would make life much simpler, and it turns out to work. The wave function yis a function of r, q, f. This is a potentially complicated function. Assume instead that y is separable, that is, a product of three functions, each of one variable only:

6. 7.2: Solution of the Schrödinger Equation for Hydrogen • Separate the resulting equation into three equations: R(r), f(θ), and g(f). • The derivatives: • Substitute: • Multiply both sides by r2 sin2θ / R f g:

7. Solution of the Schrödinger Equation for H azimuthal equation r and θ appear only on the left side and f appears only on the right side The left side of the equation cannot change as f changes. The right side cannot change with either r or θ. Each side needs to be equal to a constant for the equation to be true. Set the constant to be −mℓ2 It is convenient to choose the solution to be .

8. Solution of the Schrödinger Equation for H satisfies the azimuthal equation for any value of mℓ. The solution must be single valued to be a valid solution for any f: mℓmust be an integer (positive or negative) for this to be true. Now set the left side equal to −mℓ2 and rearrange it [divide by sin2(q)]. Now, the left side depends only on r, and the right side depends only on θ. We can use the same trick again!

9. Solution of the Schrödinger Equation for H Radial equation Angular equation We’ve separated the Schrödinger equation into three ordinary second-order differential equations, each containing only one variable. Set each side equal to the constant ℓ(ℓ + 1).

10. Solution of the Radial Equation for H • The radial equation is called the associated Laguerre equationand the solutions R are called associated Laguerre functions. There are infinitely many of them, for values of n = 1, 2, 3, … • Assume that the ground state has n = 1 and ℓ = 0. Let’s find this solution. • The radial equation becomes: • The derivative of yields two terms. • This yields:

11. Solution of the Radial Equation for H Set the second expression equal to zero and solve for a0: Set the first expression equalto zero and solve for E: Both are equal to the Bohr results! Try a solution A is a normalization constant. a0 is a constant with the dimension of length. Take derivatives of R and insert them into the radial equation. To satisfy this equation for any r, both expressions in parentheses must be zero.

12. Principal Quantum Number n • There are many solutions to the radial wave equation, one for each positive integer, n. • The result for the quantized energy is: A negative energy means that the electron and proton are bound together.

13. 7.3: Quantum Numbers • The three quantum numbers: • n: Principal quantum number • ℓ: Orbital angular momentum quantum number • mℓ: Magnetic (azimuthal) quantum number • The restrictions for the quantum numbers: • n = 1, 2, 3, 4, . . . • ℓ = 0, 1, 2, 3, . . . , n − 1 • mℓ = −ℓ, −ℓ + 1, . . . , 0, 1, . . . , ℓ − 1, ℓ • Equivalently: • n > 0 • ℓ < n • |mℓ| ≤ ℓ The energy levels are:

14. Hydrogen Atom Radial Wave Functions Sub-scripts on R specify the values of n and ℓ. First few radial wave functions Rnℓ

15. Solution of the Angular and Azimuthal Equations • The solutions to the azimuthal equation are: • Solutions to the angular and azimuthal equations are linked because both have mℓ. • Physicists usually group these solutions together into functions called Spherical Harmonics: spherical harmonics

16. Normalized Spherical Harmonics

17. Solution of the Angular and Azimuthal Equations The radial wave function R and the spherical harmonics Y determine the probability density for the various quantum states. The total wave function depends on n, ℓ, and mℓ. The wave function becomes

18. Orbital Angular Momentum Quantum Number ℓ • Energy levels are degenerate with respect to ℓ (the energy is independent of ℓ). • Physicists use letter names for the various ℓ values: • ℓ = 0 1 2 3 4 5 . . . • Letter = s p d f g h . . . • Atomic states are usualy referred to by their values of n and ℓ. • A state with n = 2 and ℓ = 1 is called a 2p state.

19. Orbital Angular Momentum Quantum Number ℓ • It’s associated with theR(r) and f(θ) parts of the wave function. • Classically, the orbital angular momentum with L = mvorbitalr. • Lis related to ℓ by • In an ℓ = 0 state, • This disagrees with Bohr’s semi-classical “planetary” model of electrons orbiting a nucleus L = nħ. Classical orbits—which do not exist in quantum mechanics

20. Magnetic Quantum Number mℓ • The angle f is the angle from the z axis. • The solution for g(f) specifies that mℓ is an integer and is related to the z component of L: Example: ℓ = 2: Only certain orientations of are possible. This is called space quantization.And (except when ℓ = 0) we just don’t know Lx and Ly!

21. Rough derivation of ‹L2› = ℓ(ℓ+1)ħ2 But Averaging over all mℓ values (assuming each is equally likely): because: We expect the average of the angular momentum components squared to be the same due to spherical symmetry:

22. 7.4: Magnetic Effects on Atomic Spectra—The Zeeman Effect • In 1896, the Dutch physicist Pieter Zeeman showed that spectral lines emitted by atoms in a magnetic field split into multiple energy levels. It is called the Zeeman effect. • Consider the atom to behave like a small magnet. • Think of an electron as an orbiting circular current loop of I = dq / dt around the nucleus. If the period is T = 2p r / v, then I = -e/T = -e/(2p r / v) = -e v /(2p r). • The current loop has a magnetic moment m = IA = [-e v /(2p r)]p r2= [-e/2m] mrv: • where L = mvr is the magnitude of the orbital angular momentum.

23. The Zeeman Effect The potential energy due to the magnetic field is: If the magnetic field is in the z-direction, we only care about the z-component of m: where mB = eħ / 2m is called the Bohr magneton.

24. The Zeeman Effect • A magnetic field splits the mℓ levels. The potential energy is quantized and now also depends on the magnetic quantum number mℓ. • When a magnetic field is applied, the 2p level of atomic hydrogen is split into three different energy states with energy difference of ΔE = mBB Δmℓ.

25. The Zeeman Effect The transition from 2p to 1s, split by a magnetic field.

26. The Zeeman Effect The mℓ = +1 state will be deflected down, the mℓ = −1 state up, and the mℓ = 0 state will be undeflected. An atomic beam of particles in the ℓ = 1 state pass through a magnetic field along the z direction.

27. 7.6: Energy Levels and Electron Probabilities • For hydrogen, the energy level depends on the prin-cipal quantum number n. In the ground state, an atom cannot emit radiation. It can absorb electromagnetic radiation, or gain energy through inelastic bombardment by particles.

28. Selection Rules We can use the wave functionsto calculate transition probabilities for the electron to change from one state to another. The probability is proportional to the mag square of the dipole moment: • Allowed transitions: • Electrons absorbing or emitting photons can change states when Δℓ = ±1 and Δmℓ = 0, ±1. • Forbidden transitions: • Other transitions are possible but occur with much smaller probabilities.

29. Probability Distribution Functions • We use the wave functions to calculate the probability distributions of the electrons. • The “position” of the electron is spread over space and is not well defined. • We may use the radial wave function R(r) to calculate radial probability distributions of the electron. • The probability of finding the electron in a differential volume element dτis .

30. Probability Distribution Functions The differential volume element in spherical polar coordinates is Therefore, At the moment, we’re only interested in the radial dependence. The radial probability density is P(r) = r2|R(r)|2 and it depends only on n and ℓ.

31. Probability Distribution Functions R(r) and P(r) for the lowest-lying states of the hydrogen atom.

32. Probability Distribution Functions The probability density for the hydrogen atom for three different electron states.

33. 7.5: Intrinsic Spin • In 1925, grad students, Samuel Goudsmit and George Uhlenbeck, in Holland proposed that the electron must have an intrinsic angular momentumand therefore a magnetic moment. • Paul Ehrenfest showed that, if so, the surface of the spinning electron should be moving faster than the speed of light! • In order to explain experimental data, Goudsmit and Uhlenbeck proposed that the electron must have an intrinsic spin quantum number s = ½.

34. Intrinsic Spin The electron’s spin will be either “up” or “down” and can never be spinning with its magnetic moment μs exactly along the z axis. The spinning electron reacts similarly to the orbiting electron in a magnetic field. The magnetic spin quantum numberms has only two values, ms = ±½.

35. Intrinsic Spin Recall: and no splitting due to . there is space quantization due to the intrinsic spin. The magnetic moment is . The coefficient of is −2μB and is a consequence of relativistic quantum mechanics. Writing in terms of the gyromagnetic ratio, g: gℓ = 1 and gs = 2: The z component of . In an ℓ = 0 state: Apply ms and the potential energy becomes:

36. Multi-electron atoms When more than one electron is involved, the potential and the wave function are functions of more than one position: Solving the Schrodinger Equation in this case can be very hard. But we can approximate the solution as the product of single-particle wave functions: And it turns out that, for electrons (and other spin ½ particles), all the Yi’s must be different. This is the Pauli Exclusion Principle.

37. Molecules have many energy levels. • A typical molecule’s energy levels: E = Eelectonic + Evibrational + Erotational 2nd excited electronic state Lowest vibrational and rotational level of this electronic “manifold” Energy 1st excited electronic state Excited vibrational and rotational level There are many other complications, such as spin-orbit coupling, nuclear spin, etc., which split levels. Transition Ground electronic state As a result, molecules generally have very complex spectra.

38. Generalized Uncertainty Principle Define theCommutatorof two operators, A and B: Then the uncertainty relation between the two corresponding observables will be: So if A and B commute, the two observables can be measured simultaneously. If not, they can’t. Example: So: and

39. Two Types of Uncertainty in Quantum Mechanics We’ve seen that some quantities (e.g., energy levels) can be computed precisely, and some not (Lx). Whatever the case, the accuracy of their measured values is limited by the Uncertainty Principle. For example, energies can only be measured to an accuracy of ħ /Dt, where Dt is how long we spent doing the measurement. And there is another type of uncertainty: we often simply don’t know which state an atom is in. For example, suppose we have a batch of, say, 100 atoms, which we excite with just one photon. Only one atom is excited, but which one? We might say that each atom has a 1% chance of being in an excited state and a 99% chance of being in the ground state. This is called a superposition state.

40. Superpositions of states Stationary states are stationary. But an atom can be in a superposition of two stationary states, and this state moves. where |ai|2 is the probability that the atom is in state i. Interestingly, this lack of knowledge means that the atom is vibrating:

41. Superpositions of states Vibrations occur at the frequency difference between the two levels. Excited level, E2 DE = hn Energy Ground level, E1 The atom is vibrating at frequency, n. The atom is at least partially in an excited state.

42. Calculations in Physics: Semi-classical physics The most precise computations are performed fully quantum-mechanically by calculating the potential precisely and solving Schrodinger’s Equation. But they can be very difficult. The least precise calculations are performed classically, neglecting quantization and using Newton’s Laws. An intermediate case is semi-classical computations, in which an atom’s energy levels are computed quantum-mechanically, but additional effects, such as light waves, are treated classically. Our Thomson Scattering calculation of a and n was an example of this.