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Atomic Vibrations in Crystals = Phonons Hooke’s law: Vibration frequency f M f = force constant, M = mass Test for phonon effects by using isotopes with different mass, for example in superconductivity, where electron pairs are formed by the electron-phonon interaction. modes Transverse modes (Oscillating Dipole) r Classical vs. quantum vibrations in a molecule r r Quantum probability Classical probability Anharmonic oscillator and thermal expansion A realistic potential energy curve between two atoms is asymmetric: short-range Pauli repulsion versus long-range Coulomb attraction (see Lect. 5, p. 4): U(r) (r)2 (r)3 … Harmonic Anharmonic T>0 T=0 a This asymmetry causes anharmonic oscillations. The probability density ||2 shifts towards larger r for the higher vibrational levels. These are excited at higher temperature. The symmetric potential of the harmonic oscillator does not produce such a shift. Measuring phonons by inelastic (E≠0) neutron scattering E,k Energy and momentum conservation: E = E0 Ephon E0,k0 k = k0 kphon + Ghkl Ephon, kphon Bragg reflection makes neutrons (and X-rays) monochromatic. Triple-axis spectrometer: k E0 E Measuring phonons by inelastic photon scattering (Raman Spectroscopy) Tphonon photon phonon Tphoton The phonon wave modulates the light wave, creating side bands (like AM radio). Measuring phonons by inelastic electron scattering Electron Energy Loss Spectroscopy (EELS) Probing Depth: Neutrons: cm Photons: m-cm Electrons: nm Electrons interact very strongly with optical phonons in ionic solids. That gives rise to multiple phonon losses.