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Arevik Amiryan

Publications and source records attributed to Arevik Amiryan.

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Observation of Magnetically-Induced atomic transitions of the Cs 6S$_{1/2} \rightarrow 7$P$_{3/2}$ line at 456 nm

It has recently been demonstrated that magnetically induced (MI) transitions, a class of transitions forbidden at zero magnetic field, of the Cs 6$^2$S$_{1/2} \rightarrow 6^2$P$_{3/2}$ (D$_2$) line, exhibit promising features for high-resolution physics applications in the near-infrared range. In this work, we study a group of seven MI transitions ($F_g = 3 \rightarrow F_e = 5$) of the Cs $6^2$S$_{1/2} \rightarrow 7^2$P$_{3/2}$ line at $λ= 456$ nm. The experimental measurements are in very good agreement with theoretical predictions based on the diagonalization of the Zeeman Hamiltonian. In magnetic fields ranging from $0.2-3$ kG, these transitions reach a maximum intensity above that of conventional transitions. Another noteworthy property is their large frequency shift, reaching approximately $17~\mathrm{GHz}$ with respect to the unperturbed hyperfine transitions in magnetic fields of about $3~\mathrm{kG}$. These interesting properties may prove useful for the realization of optical frequency references or magnetometers with sub-micron spatial resolution in the blue region of the spectrum.

physics.atom-ph

Coherent Optical Processes on Cs D$_2$ line Magnetically Induced Transitions

The increased spectral resolution allowed by the use of extremely thin vapor cells has led to the observation of interesting behaviour of alkali transitions when placed in a magnetic field. Particularly, transitions obeying an apparent $F_e-F_g\equivΔF =\pm2$ selection rule, referred to as magnetically-induced (MI) transitions, have their probabilities largely increase in the intermediate interaction regime while being null at zero and higher magnetic fields. With an 800 nm-thick Cs vapor cell placed in a field up to 1.5 kG, we show here that the generation of electromagnetically induced transparency (EIT), realized in $Λ$-systems involving $ΔF =- 2$ MI transitions, is only possible when both the coupling and probe beams are $σ^-$-circular polarized, demonstrating that EIT is affected by magnetic circular dichroism. A similar rule of thumb can be extrapolated for $ΔF =+2$ MI transitions and $σ^+$ polarization. Because of the high frequency shift slope (typ. 4 MHz/G), the generation of EIT resonances involving MI transitions is interesting, especially in the context of growing attention towards micro-machined alkali vapor cell sensors.

physics.atom-ph

Circular dichroism in atomic vapors: magnetically induced transitions responsible for two distinct behaviors

Atomic transitions of alkali metals for which the condition $F_e-F_g = \pm2$ is satisfied have null probability in a zero magnetic field, while a giant increase can occur when an external field is applied. Such transitions, often referred to as magnetically-induced (MI) transitions, have received interest because their high probabilities in wide ranges of external magnetic fields which, in some cases, are even higher than that of usual atomic transitions. Previously, the following rule was established: the intensities of MI transitions with $ΔF=\pm2$ are maximum when using respectively $σ^\pm$ radiation. Within the same ground state, the difference in intensity for $σ^+$ and $σ^-$ radiations can be significant, leading to magnetically induced circular dichroism (MCD), referred to as type-1. Here, we show that even among the strongest MI transitions, $i.e$ originating from different ground states for $σ^+$ and $σ^-$, the probability of MI transition with $ΔF = + 2$ is always greater, which leads to another type of MCD. Our experiments are performed with a Cs-filled nanocell, where the laser is tuned around the D$_2$ line; similar results are expected with other alkali metals. Theoretical calculations are in excellent agreement with the experimental measurements.

physics.atom-ph

Features of Magnetically-induced atomic transitions of Rb D$_1$ line studied by Doppler-free method based on the second derivative of the absorption spectra

We show that the Second Derivative (SD) technique of the absorption spectra of Rb atomic vapours confined in a nanocell with a thickness $\ell= λ/2=398$ nm allows to achieve close to Doppler-free spectroscopy. Narrow linewidth and linearity of the SD signal response with respect to transition probabilities allow us to study separately, in an external transverse magnetic field (0.6 to 4 kG), a big number of the atomic transitions of $^{85}$Rb and $^{87}$Rb atoms. Atomic transitions $|F_g,0\rangle \rightarrow |F_e=F_g,0'\rangle$, for which the dipole moment is null at zero magnetic field (so-called magnetically-induced transitions), show a gigantic increase in probability with increasing magnetic field. When a magnetic field is applied on the vapour, we show the possibility of forming a dark resonance on these transitions by adding a coupling laser. We hence demonstrate a five-fold increase in the transmission of the probe radiation when the coupling laser is on. Theoretical calculations are in a very good agreement with experimental results.

physics.atom-ph

Resolution-enhanced quantitative spectroscopy of atomic vapor in optical nanocells based on second-derivative processing of spectra

We present a method for recovery of narrow homogeneous spectral features out of broad inhomogeneous overlapped profile based on second-derivative processing of the absorption spectra of alkali metal atomic vapor nanocells. The method is shown to preserve the frequency positions and amplitudes of spectral transitions, thus being applicable for quantitative spectroscopy. The proposed technique was successfully applied and tested for: measurements of hyperfine splitting and atomic transition probabilities; development of an atomic frequency reference; determination of isotopic abundance; study of atom-surface interaction; and determination of magnetic field-induced modification of atomic transitions frequency and probability. The obtained experimental results are fully consistent with theoretical modeling.

physics.atom-ph