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5.2 Perturbation theory: time-independent and time-dependent

5.2 Perturbation theory: time-independent and time-dependent

Written by the Fiveable Content Team โ€ข Last updated August 2025
Written by the Fiveable Content Team โ€ข Last updated August 2025
โš—๏ธTheoretical Chemistry
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Perturbation theory helps solve complex quantum systems by tweaking simpler ones. It's like figuring out how a small change affects a well-understood system, giving us insights into trickier problems without solving them directly.

This method comes in two flavors: time-independent for static systems and time-dependent for dynamic ones. Both are crucial for understanding how particles behave when nudged by external forces or fields in quantum chemistry.

Perturbation Theory Fundamentals

Perturbation Hamiltonian and Zeroth-Order Approximation

  • Perturbation theory is a method for finding approximate solutions to the Schrรถdinger equation when the Hamiltonian can be split into two parts: H=H(0)+ฮปVH = H^{(0)} + \lambda V
    • H(0)H^{(0)} is the unperturbed Hamiltonian, which has known eigenstates and eigenvalues
    • ฮปV\lambda V is the perturbation, where ฮป\lambda is a small parameter and VV is the perturbation operator
  • The zeroth-order approximation assumes that the eigenstates and eigenvalues of the perturbed system are the same as those of the unperturbed system
    • Eigenstates: ฯˆn(0)=ฯ•n\psi_n^{(0)} = \phi_n, where ฯ•n\phi_n are the eigenstates of H(0)H^{(0)}
    • Eigenvalues: En(0)=ฮตnE_n^{(0)} = \varepsilon_n, where ฮตn\varepsilon_n are the eigenvalues of H(0)H^{(0)}
  • Examples of unperturbed Hamiltonians include the particle in a box and the harmonic oscillator

First-Order and Second-Order Corrections

  • The first-order correction to the energy is given by En(1)=โŸจฯ•nโˆฃVโˆฃฯ•nโŸฉE_n^{(1)} = \langle \phi_n | V | \phi_n \rangle
    • This is the expectation value of the perturbation operator in the unperturbed state
    • The first-order corrected energy is Enโ‰ˆEn(0)+En(1)E_n \approx E_n^{(0)} + E_n^{(1)}
  • The first-order correction to the wavefunction is given by ฯˆn(1)=โˆ‘mโ‰ nโŸจฯ•mโˆฃVโˆฃฯ•nโŸฉEn(0)โˆ’Em(0)ฯ•m\psi_n^{(1)} = \sum_{m \neq n} \frac{\langle \phi_m | V | \phi_n \rangle}{E_n^{(0)} - E_m^{(0)}} \phi_m
    • This is a sum over all unperturbed states except ฯ•n\phi_n, weighted by the matrix elements of the perturbation and the energy differences
  • The second-order correction to the energy is given by En(2)=โˆ‘mโ‰ nโˆฃโŸจฯ•mโˆฃVโˆฃฯ•nโŸฉโˆฃ2En(0)โˆ’Em(0)E_n^{(2)} = \sum_{m \neq n} \frac{|\langle \phi_m | V | \phi_n \rangle|^2}{E_n^{(0)} - E_m^{(0)}}
    • This involves a sum over all unperturbed states except ฯ•n\phi_n, with each term being the square of the perturbation matrix element divided by the energy difference
  • Examples of perturbations include an electric field applied to a hydrogen atom (Stark effect) or a magnetic field applied to a spin system (Zeeman effect)
Perturbation Hamiltonian and Zeroth-Order Approximation, quantum mechanics - Perturbation Theory Problem - Physics Stack Exchange

Advanced Perturbation Techniques

Degenerate Perturbation Theory

  • Degenerate perturbation theory is used when the unperturbed system has degenerate energy levels (multiple states with the same energy)
  • In this case, the perturbation can lift the degeneracy, and the first-order correction to the energy is found by diagonalizing the perturbation matrix within the degenerate subspace
  • The eigenstates of the perturbed system are linear combinations of the degenerate unperturbed states
  • Examples of degenerate systems include the 2p2p orbitals of hydrogen or the dd orbitals in a cubic crystal field
Perturbation Hamiltonian and Zeroth-Order Approximation, quantum mechanics - harmonic oscillator relation with this hamiltonian - Physics Stack Exchange

Time-Dependent Perturbation Theory

  • Time-dependent perturbation theory is used when the perturbation is time-dependent, such as an oscillating electric field
  • The time-dependent Schrรถdinger equation is iโ„โˆ‚ฯˆ(t)โˆ‚t=[H(0)+V(t)]ฯˆ(t)i\hbar \frac{\partial \psi(t)}{\partial t} = [H^{(0)} + V(t)] \psi(t)
  • The wavefunction can be expanded in the basis of unperturbed states: ฯˆ(t)=โˆ‘ncn(t)ฯ•neโˆ’iEn(0)t/โ„\psi(t) = \sum_n c_n(t) \phi_n e^{-i E_n^{(0)} t / \hbar}
    • The coefficients cn(t)c_n(t) are time-dependent and satisfy a set of coupled differential equations
  • Examples of time-dependent perturbations include the interaction of an atom with a laser field or the absorption of a photon by a molecule

Time-Dependent Perturbation Theory

Interaction Picture and Fermi's Golden Rule

  • The interaction picture is a useful formalism for time-dependent perturbation theory
    • The wavefunction is transformed as ฯˆI(t)=eiH(0)t/โ„ฯˆ(t)\psi_I(t) = e^{i H^{(0)} t / \hbar} \psi(t)
    • The Schrรถdinger equation in the interaction picture is iโ„โˆ‚ฯˆI(t)โˆ‚t=VI(t)ฯˆI(t)i\hbar \frac{\partial \psi_I(t)}{\partial t} = V_I(t) \psi_I(t), where VI(t)=eiH(0)t/โ„V(t)eโˆ’iH(0)t/โ„V_I(t) = e^{i H^{(0)} t / \hbar} V(t) e^{-i H^{(0)} t / \hbar}
  • Fermi's golden rule gives the transition rate from an initial state ii to a final state ff under a perturbation VV: ฮ“iโ†’f=2ฯ€โ„โˆฃโŸจfโˆฃVโˆฃiโŸฉโˆฃ2ฯ(Ef)\Gamma_{i \to f} = \frac{2\pi}{\hbar} |\langle f | V | i \rangle|^2 \rho(E_f)
    • ฯ(Ef)\rho(E_f) is the density of states at the final energy EfE_f
    • This rule is valid for weak perturbations and long times (first-order time-dependent perturbation theory)
  • Examples of processes described by Fermi's golden rule include spontaneous emission, photoelectric effect, and Raman scattering