Muneaki Hase

Optical control of coherent optical phonons in bismuth films

Interference of impulsively excited coherent phonons in semimetals has been studied by using a double‐pulse pump–probe technique. Enhancement of the oscillation amplitude of an A1g mode is observed when the separation time of the double‐pulse is matched to the period of the phonon oscillation, and a cancellation is observed when the separation time is adjusted to half the period of the phonon oscillation. The amplitude after the second pulse shows a sinusoidal dependence as a function of the separation time, and this dependence is explained in terms of a superposition of two coherent phonon oscillations. In addition, not only the A1g mode but also an Eg mode have been observed by electro‐optic sampling.

The birth of a quasiparticle in silicon observed in time-frequency space

The concept of quasiparticles in solid-state physics is an extremely powerful tool for describing complex many-body phenomena in terms of single-particle excitations. Introducing a simple particle, such as an electron, hole or phonon, deforms a many-body system through its interactions with other particles. In this way, the added particle is ‘dressed’ or ‘renormalized’ by a self-energy cloud that describes the response of the many-body system, so forming a new entity—the quasiparticle. Using ultrafast laser techniques, it is possible to impulsively generate bare particles and observe their subsequent dressing by the many-body interactions (that is, quasiparticle formation) on the time and energy scales governed by the Heisenberg uncertainty principle. Here we describe the coherent response of silicon to excitation with a 10-femtosecond (10-14 s) laser pulse. The optical pulse interacts with the sample by way of the complex second-order nonlinear susceptibility to generate a force on the lattice driving coherent phonon excitation. Transforming the transient reflectivity signal into frequency–time space reveals interference effects leading to the coherent phonon generation and subsequent dressing of the phonon by electron–hole pair excitations.

Ultrafast Electron-Phonon Decoupling in Graphite

We report the ultrafast dynamics of the 47.4 THz coherent phonons of graphite interacting with a photoinduced non-equilibrium electron-hole plasma. Unlike conventional materials, upon photoexcitation the phonon frequency of graphite upshifts, and within a few picoseconds relaxes to the stationary value. Our first-principles density functional calculations demonstrate that the phonon stiffening stems from the light-induced decoupling of the non-adiabatic electron-phonon interaction by creating the non-equilibrium electron-hole plasma. Time-resolved vibrational spectroscopy provides a window on the ultrafast non-equilibrium electron dynamics.

Coherent optical phonons in diamond

The authors report femtosecond dynamics of the coherent optical phonon of single crystal diamond. Sub-10fs, 395nm laser pulses excite 40THz coherent phonons with an extremely small damping rate (0.15ps−1). Linear power dependence of the phonon amplitude under off-resonant excitation condition gives a direct evidence for an eletric-field-driven generation mechanism. The coherent phonon generation is noticeably suppressed by doping with nitrogen impurities, in spite of their absorption in the near ultraviolet. The present study demonstrates that a simple pump-probe technique can be a powerful tool for evaluating the ultrafast coherent electronic and lattice dynamics of diamond materials.

Mirror-symmetric magneto-optical Kerr rotation using visible light in [(GeTe)2(Sb2Te3)1]n topological superlattices.

Interfacial phase change memory (iPCM), that has a structure of a superlattice made of alternating atomically thin GeTe and Sb2Te3 layers, has recently attracted attention not only due to its superior performance compared to the alloy of the same average composition in terms of energy consumption but also due to its strong response to an external magnetic field (giant magnetoresistance) that has been speculated to arise from switching between topological insulator (RESET) and normal insulator (SET) phases. Here we report magneto-optical Kerr rotation loops in the visible range, that have mirror symmetric resonances with respect to the magnetic field polarity at temperatures above 380 K when the material is in the SET phase that has Kramers-pairs in spin-split bands. We further found that this threshold temperature may be controlled if the sample was cooled in a magnetic field. The observed results open new possibilities for use of iPCM beyond phase-change memory applications.

Ultrafast dynamics of coherent optical phonons and nonequilibrium electrons in transition metals

The femtosecond optical pump-probe technique was used to study dynamics of photoexcited electrons and coherent optical phonons in transition metals Zn and Cd as a function of temperature and excitation level. The optical response in time domain is well fitted by linear combination of a damped harmonic oscillation because of excitation of coherent

Ultrafast dephasing of coherent optical phonons in atomically controlled GeTe/Sb2Te3 superlattices

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Dephasing of coherent phonons by lattice defects in bismuth films

phonon and a subpicosecond transient response due to electron-phonon thermalization. The electron-phonon thermalization time monotonically increases with temperature, consistent with the thermomodulation scenario, where at high temperatures the system can be well explained by the two-temperature model, while below

Interaction of coherent phonons with defects and elementary excitations

\ensuremath{\approx}50\phantom{\rule{0.3em}{0ex}}\mathrm{K}

Ultrafast carrier and phonon dynamics in ion-irradiated graphite

the nonthermal electron model needs to be applied. As the lattice temperature increases, the damping of the coherent