A Step Closer To Visualizing The Electron Phonon Interplay PDF Download

The origin of the very high superconducting transition temperature (Tc) in ceramic copper oxide superconductors is one of the greatest mysteries in modern physics. In the superconducting state, electrons form pairs (known as Cooper pairs) and condense into the superfluid state to conduct electric current with zero resistance. For conventional superconductors, it is well established that the 2 electrons in a Cooper pair are 'bonded' by lattice vibrations (phonons), whereas in high-Tc superconductors, the 'glue' for the Cooper pairs is still under intense discussion. Although the high transition temperature and the unconventional pairing symmetry (d-wave symmetry) have led many researchers to believe that the pairing mechanism results from electron-electron interaction, increasing evidence shows that electron-phonon coupling also significantly influences the low-energy electronic structures and hence may also play an important role in high-Tc superconductivity. In a recent issue of PNAS, Carbone et al. use ultrafast electron diffraction, a recently developed experimental technique, to attack this problem from a new angle, the dynamics of the electronic relaxation process involving phonons. Their results provide fresh evidence for the strong interplay between electronic and atomic degrees of freedom in high-Tc superconductivity. In general, ultrafast spectroscopy makes use of the pump-probe method to study the dynamic process in material. In such experiments, one first shoots an ultrafast (typically 10-100 fs) 'pumping' pulse at the sample to drive its electronic system out of the equilibrium state. Then after a brief time delay ([Delta]t) of typically tens of femtoseconds to tens of picoseconds, a 'probing' pulse of either photons or electrons is sent in to probe the sample's transient state. By varying [Delta]t, one can study the process by which the system relaxes back to the equilibrium state, thus acquiring the related dynamic information. This pump-probe experiment is reminiscent of the standard method used by bell makers for hundreds of years to judge the quality of their products (hitting a bell then listening to how the sound would fade away), albeit the relevant time scale here is way beyond tens of femtoseconds. Traditionally, ultrafast spectroscopy was carried out to study gas-phase reactions, but it has also been applied to study condensed phase systems since the development of reliable solid-state ultrafast lasers approximately a decade ago. In addition, the ability to control pulse width, wavelength, and amplification of the output of Ti:Sapphire lasers has further increased the capability of this experimental method. During the past decade, many ultrafast pump-probe experiments have been carried out in various fields by using different probing methods, such as photo-resistivity, fluorescence yield, and photoemission, and they have revealed much new information complementary to the equilibrium spectroscopy methods used before. Carbone et al. used the photon-pump, electron (diffraction)-probe method. The pumping photon pulse first drives the electrons in the sample into an oscillating mode along its polarization direction. Then during the delay time, these excited electrons can transfer excess energy to the adjacent nuclei and cause crystal lattice vibration on their way back to the equilibrium state. An ultrashort electron pulse is shot at the sample at various time delays [Delta]t and the diffraction pattern is collected. Because the electron diffraction pattern is directly related to the crystal lattice structure and its motion, this technique provides a natural way to study the electron-phonon coupling problem. Furthermore, by adjusting the pump pulse's relative polarization with respect to the Cu-O bond direction, Carbone et al. were able to acquire the electron-phonon coupling strength along different directions. Focusing on the lattice dynamic along the c axis, Carbone et al. found that the c-axis phonons in the optimally-doped Bi2Sr2CaCu2O (Bi2212) are coupled to the electrons with different strength along different directions within the CuO2 plane. The coupling strength reaches its largest value along the 2 Cu-O bond directions and becomes the weakest along the bisector of the angle formed by the 2 Cu-O bonds. As pointed out by Carbone et al., these observations agree well with the calculated coupling strength between electrons and the buckling phonons. Furthermore, their observation of this anisotropic electron-phonon coupling also agrees with results from angle-resolved photoemission (ARPES), which measures the equilibrium-state properties of materials. In ARPES measurements, electron-phonon coupling manifests itself as a kink anomaly in the band dispersion and a corresponding sudden broadening in the spectral width.