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We investigate the effect of incoherent perturbations on atomic photoionization due to a femtosecond mid-infrared laser pulse by solving the time-dependent stochastic Schrodinger equation. For a weak laser pulse which causes almost no ionization, an addition of a Gaussian white noise to the pulse leads to a significantly enhanced ionization probability. Tuning the noise level, a stochastic resonance-like curve is observed showing the existence of an optimum noise for a given laser pulse. Besides studying the sensitivity of the obtained enhancement curve on the pulse parameters, such as the pulse duration and peak amplitude, we suggest that experimentally realizable broadband chaotic light can also be used instead of the white noise to observe similar features. The underlying enhancement mechanism is analyzed in the frequency-domain by computing a frequency-resolved atomic gain profile, as well as in the time-domain by controlling the relative delay between the action of the laser pulse and noise.
We develop a formalism for photoionization (PI) and potential energy curves (PECs) of Rydberg atoms in ponderomotive optical lattices and apply it to examples covering several regimes of the optical-lattice depth. The effect of lattice-induced PI on
We study the robustness of geometric phase in the presence of parametric noise. For that purpose we consider a simple case study, namely a semiclassical particle which moves adiabatically along a closed loop in a static magnetic field acquiring the D
Simultaneous quantum estimation of multiple parameters has recently become essential in quantum metrology. Although the ultimate sensitivity of a multiparameter quantum estimation in noiseless environments can beat the standard quantum limit that eve
Photoionization of a cold atomic sample offers intriguing possibilities to observe collective effects at extremely low temperatures. Irradiation of a rubidium condensate and of cold rubidium atoms within a magneto-optical trap with laser pulses ioniz
We measure the photoionization cross-section of vibrationally excited levels in the S2 state of azulene by femtosecond pump-probe spectroscopy. At the wavelengths studied (349-265 nm in the pump) the transient signals exhibit two distinct and well-de