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Oleg V. Misochko

Publications and source records attributed to Oleg V. Misochko.

9 recordsLinked to original sources

Suppression of shear ionic motions in bismuth by coupling with large-amplitude internal displacement

Bismuth, with its rhombohedral crystalline structure and two Raman active phonon modes corresponding to the internal displacement ($A_{1g}$) and shear ($E_{g}$) ionic motions, offers an ideal target for the investigation of the phonon-phonon and electron-phonon couplings under photoexcitation. We perform transient reflectivity measurements of bismuth single crystal at 11 K over wide range of absorbed laser fluence up to $F_\text{abs}=9$ mJ/cm$^2$, at which a sign of an irreversible surface damage is observed. At the minimum fluence examined (0.1 mJ/cm$^2$) the coherent $A_{1g}$ and $E_g$ oscillations are a cosine and a sine functions of time, as are consistent with their generations in the displacive and impulsive limits, respectively. With increasing fluence the initial phases of the both modes deviate from their low-fluence values, indicating a finite time required for the transition from the ground-state potential energy surface (PES) to the excited-state one. Surprisingly, the $E_g$ amplitude increases with increasing fluence up to 3 mJ/cm$^2$ and then turns to an apparent decrease, in contrast to the monotonic increase of the $A_{1g}$ amplitude up to 6 mJ/cm$^2$. The contrasted behaviors can be understood by considering a two-dimensional PES, where the strongly driven $A_{1g}$ oscillation leads to a temporal fluctuation of the PES along the $E_g$ coordinate and thereby to a loss in the $E_g$ oscillation coherence at high fluences.

cond-mat.mtrl-sci↗

Photo-Induced Ultrafast Symmetry Switch in SnSe

Layered tin selenide (SnSe) has recently emerged as a high-performance thermoelectric material with the current record for the figure of merit (ZT) observed in the high-temperature Cmcm phase. So far, access of the Cmcm phase has been mainly obtained via thermal equilibrium methods based on sample heating or application of external pressure, thus restricting the current understanding only to ground-state conditions. Here, we investigate the ultrafast carrier and phononic dynamics in SnSe. Our results demonstrate that optical excitations can transiently switch the point-group symmetry of the crystal from Pnma to Cmcm at room temperature in a few hundreds of femtoseconds with an ultralow threshold for the excitation carrier density. This non-equilibrium Cmcm phase is found to be driven by the displacive excitation of coherent Ag phonons and, given the absence of low-energy thermal phonons, exists in SnSe with the status of 'cold lattice with hot carriers'. Our findings provide important insight for understanding non-equilibrium thermoelectric properties of SnSe.

cond-mat.mtrl-sci↗

Temperature effect on the coupling between coherent longitudinal phonons and plasmons in n- and p-type GaAs

The coupling between longitudinal optical (LO) phonons and plasmons plays a fundamental role in determining the performance of doped semiconductor devices. In this work, we report a comparative investigation into the dependence of the coupling on temperature and doping in n- and p-type GaAs by using ultrafast optical phonon spectroscopy. A suppression of coherent oscillations has been observed in p-type GaAs at lower temperature, strikingly different from n-type GaAs and other materials in which coherent oscillations are strongly enhanced by cooling. We attribute this unexpected observation to a cooling-induced elongation of the depth of the depletion layer which effectively increases the screening time of surface field due to a slow diffusion of photoexcited carriers in p-type GaAs. Such an increase breaks the requirement for the generation of coherent LO phonons and, in turn, LO phonon-plasmon coupled modes because of their delayed formation in time.

cond-mat.mtrl-sci↗

Femtosecond study of A1g phonons in the strong 3D topological insulators: From pump-probe to coherent control

Fully symmetric A1g phonons are expected to play a dominant role in electron scattering in strong topological insulators (TIs), thus limiting the ballistic transport of future electronic devices. Here, we report on femtosecond time-resolved observation of a pair of A1g coherent phonons and their optical control in two strong 3D TIs, Bi2Te3 and Bi2Se3, by using a second pump pulse in ultrafast spectroscopy measurements. Along with well-defined phonon properties such as frequency and lifetime, an obvious phonon chirp has been observed, implying a strong coupling between photo-carriers and lattices. The coherent phonon manipulation, on the other hand, allows us to change the phonon amplitude selectively but does not affect either the frequency or coherence lifetime of the chosen mode.

cond-mat.mes-hall↗

Delayed formation of coherent LO phonon-plasmon coupled modes in n-type and p-type GaAs measured using a femtosecond coherent control technique

Coherent control experiments using a pair of collinear femtosecond laser pulses have been carried out to manipulate longitudinal optical (LO) phonon-plasmon coupled (LOPC) modes in both p- and n-type GaAs. By tuning the interpulse separation, remarkably distinct responses have been observed in the two samples. To understand the results obtained a phenomenological model taking the delayed formation of coherent LOPC modes into account is proposed. The model suggests that the lifetime of coherent LOPC modes plays a key role and the interference of the coherent LO phonons excited successively by two pump pulses strongly affects the manipulation of coherent LOPC modes.

cond-mat.mtrl-sci↗

Ultrafast electronic and lattice dynamics in laser-excited crystalline bismuth

Femtosecond spectroscopy is applied to study transient electronic and lattice processes in bismuth. Components with relaxation times of 1 ps, 7 ps and ~ 1 ns are detected in the photoinduced reflectivity response of the crystal. To facilitate the assignment of the observed relaxation to the decay of particular excited electronic states we use pump pulses with central wavelengths ranging from 400 nm to 2.3 mum. Additionally, we examine the variation of parameters of coherent A1g phonons upon the change of excitation and probing conditions. Data analysis reveals a significant wavevector dependence of electron-hole and electron- phonon coupling strength along Γ--T direction of the Brillouin zone.

cond-mat.mtrl-sci↗

Direct observation of two-phonon bound states in ZnTe

A coherent two-phonon bound state has been impulsively generated in ZnTe(110) via second-order Raman scattering in the time domain for the first time. The two-phonon bound state, composed of two anticorrelated in wave vector acoustic phonons, exhibits full Γ1 symmetry and has energy higher than the corresponding 2TA(X) overtone. By suppressing two-phonon fluctuations with a double-pulse excitation, the coexistence of coherently excited bound and unbound two-phonon states has been demonstrated.

cond-mat.mtrl-sci↗

Controlling phonon squeezing and correlation via one- and two-phonon interference

When ultrafast laser pulse strikes the crystal with a van Hove singularity in the phonon density of states, it can create a pair of anti-correlated in wave-vector acoustic phonons. As a result, the atomic fluctuations in either position or momentum become squeezed in such a way that their size might fall below the vacuum level. The ultrafast pulses can also generate a two-phonon bound (biphonon) state in which the constituent phonons are correlated and/or entangled. Here we show that via the interplay between one- and two-phonon interference the bound and squeezed two-phonon state in (110) oriented ZnTe single crystal can be manipulated. We demonstrate experimentally that when two biphonon ensembles are temporally and spatially overlapped, the strength of phonon squeezing and correlation can be controlled. However, due to the complementarity of one- and two-phonon interference a larger correlation comes at the expense of a reduced squeezing.

cond-mat.mtrl-sci↗

Probing ultrafast symmetry breaking in photo-stimulated matter

The nature of a phase transition is inherently connected to the changes in the crystalline symmtry, which is typically probed by elastic or inelastic scattering with neutrons, electrons or photons. When such a phase transition is stimulated by light or other sudden perturbations the solid evolves along a non-equilibrium pathway of which the underlying physics is poorly understood. Here we use picosecond Raman scattering to study the photo-induced ultrafast dynamics in Peierls distorted Antimony. We find evidence for an ultrafast non-thermal reversible structural phase transition. Most surprisingly, we find evidence that this transition evolves toward a lower symmetry, in contrast to the commonly accepted rhombohedral-to-simple cubic transition path. Our study demonstrates the feasibility of ultrafast Raman scattering symmetry analysis of photo-induced non-thermal transient phases.

cond-mat.mtrl-sci↗