arXiv subjects

V. Milner

Publications and source records attributed to V. Milner.

24 records · Page 2Linked to original sources

arXiv2011

Strong-field effects in Rabi oscillations between a single state and a superposition of states

Rabi oscillations of quantum population are known to occur in two-level systems driven by spectrally narrow laser fields. In this work we study Rabi oscillations induced by shaped broadband femtosecond laser pulses. Due to the broad spectral width of the driving field, the oscillations are initiated between a ground state and a coherent superposition of excited states, or a "wavepacket", rather than a single excited state. Our experiments reveal an intricate dependence of the wavepacket phase on the intensity of laser field. We confirm numerically that the effect is associated with the strong-field nature of the interaction, and provide a qualitative picture by invoking a simple theoretical model.

quant-ph↗

arXiv2011

Control of molecular rotation with a chiral train of ultrashort pulses

Trains of ultrashort laser pulses separated by the time of rotational revival (typically, tens of picoseconds) have been exploited for creating ensembles of aligned molecules. In this work we introduce a chiral pulse train - a sequence of linearly polarized pulses with the polarization direction rotating from pulse to pulse by a controllable angle. The chirality of such a train, expressed through the period and direction of its polarization rotation, is used as a new control parameter for achieving selectivity and directionality of laser-induced rotational excitation. The method employs chiral trains with a large number of pulses separated on the time scale much shorter than the rotational revival (a few hundred femtosecond), enabling the use of conventional pulse shapers.

quant-ph↗

arXiv2009

Complete transfer of populations from a single state to a pre-selected superposition of states using Piecewise Adiabatic Passage: Experiment

We demonstrate a method of adiabatic population transfer from a single quantum state into a coherent superposition of states. The transfer is executed with femtosecond pulses, spectrally shaped in simple and intuitive manner, which does not require iterative feedback-controlled loops. In contrast to non-adiabatic methods of excitation, our approach is not sensitive to the exact value of laser intensity. We show that the population transfer is complete, and analyze the possibility of controlling the relative phases and amplitudes of the excited eigenstates. We discuss the limitations of the proposed control methods due to the dynamic level shifts and suggest ways of reducing their influence.

quant-ph↗

arXiv2007

Noise auto-correlation spectroscopy with coherent Raman scattering

Ultrafast lasers have become one of the most powerful tools in coherent nonlinear optical spectroscopy. Short pulses enable direct observation of fast molecular dynamics, whereas broad spectral bandwidth offers ways of controlling nonlinear optical processes by means of quantum interferences. Special care is usually taken to preserve the coherence of laser pulses as it determines the accuracy of a spectroscopic measurement. Here we present a new approach to coherent Raman spectroscopy based on deliberately introduced noise, which increases the spectral resolution, robustness and efficiency. We probe laser induced molecular vibrations using a broadband laser pulse with intentionally randomized amplitude and phase. The vibrational resonances result in and are identified through the appearance of intensity correlations in the noisy spectrum of coherently scattered photons. Spectral resolution is neither limited by the pulse bandwidth, nor sensitive to the quality of the temporal and spectral profile of the pulses. This is particularly attractive for the applications in microscopy, biological imaging and remote sensing, where dispersion and scattering properties of the medium often undermine the applicability of ultrafast lasers. The proposed method combines the efficiency and resolution of a coherent process with the robustness of incoherent light. As we demonstrate here, it can be implemented by simply destroying the coherence of a laser pulse, and without any elaborate temporal scanning or spectral shaping commonly required by the frequency-resolved spectroscopic methods with ultrashort pulses.

physics.chem-ph↗

arXiv2007

Population transfer between two quantum states by piecewise chirping of femtosecond pulses: Theory and experiment

We propose and demonstrate the method of population transfer by piecewise adiabatic passage between two quantum states. Coherent excitation of a two-level system with a train of ultrashort laser pulses is shown to reproduce the effect of an adiabatic passage, conventionally achieved with a single frequency-chirped pulse. By properly adjusting the amplitudes and phases of the pulses in the excitation pulse train, we achieve complete and robust population transfer to the target state. The effect is demonstrated experimentally by observing piecewise excitation of Rubidium atoms from 5s_1/2 to 5p_1/2 electronic state. We show that similarly to the conventional adiabatic passage, the piecewise process is insensitive to the total excitation energy as long as the adiabaticity conditions are satisfied. The piecewise nature of the process suggests that robust and selective population transfer could be implemented in a variety of complex quantum systems beyond the two-level approximation.

physics.atom-ph↗

arXiv2004

Photon localization laser

We demonstrate low-threshold random lasing in random amplifying layered medium via photon localization. Lasing is facilitated by resonant excitation of localized modes at the pump laser wavelength, which are peaked deep within the sample with greatly enhanced intensity. Emission occurs into long-lived localized modes overlapping the localized gain region. This mechanism overcomes a fundamental barrier to reducing lasing thresholds in diffusive random lasers, in which multiple scattering restricts the excitation region to the proximity of the sample surface.

physics.optics↗