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G. O. Ariunbold

Publications and source records attributed to G. O. Ariunbold.

3 recordsLinked to original sources

Multi-channel collective dissipation via the symmetric irreducible representation of SU(4)

We specialize Agarwal's multi-level collective spontaneous-emission formalism to the four-level case by formulating it in the fully symmetric \SU(4) representation of $N$ identical atoms. In the irreducible representation $(N,0,0)$, the occupation-number basis forms a tetrahedral weight lattice on which the six embedded $\mathfrak{su}(2)$ transition subalgebras act as ladder operators. From these algebraic factors we obtain a compact Pauli-type population-rate equation and a closed-form expression for the total emitted intensity that apply to any combination of open dipole channels. The formalism is then specialized to the seven dipole-allowed four-level topologies -- tripod, inverted tripod, Y, inverted Y, double-$Λ$, closed cascade, and diamond -- and the resulting rate equations are solved numerically for atom numbers up to $N=50$. In every case the emitted intensity develops a delayed cooperative burst whose peak height obeys a power law $I_{\mathrm{peak}}=aN^{p}$ with topology-dependent parameters $(a,p)$; the fitted exponents lie in the range $1.81\lesssim p\lesssim 1.92$, indicating a superlinear. The \SU(4) tetrahedral flow and the seven configuration-dependent transients together provide a unified geometric picture of multi-channel collective dissipation in four-level atomic ensembles.

quant-ph

Nonclassical Imaging for a quantum search of trapped ions

We discuss a simple search problem which can be pursued with different methods, either on a classical or on a quantum basis. The system is represented by a chain of trapped ions. The ion to be searched is a member of that chain, consists, however, of an isotopic species different to the others. It is shown that the classical imaging may lead as fast to the final result as the quantum imaging. However, for the discussed case the quantum method gives more flexibility and higher precision when the number of ions considered in the chain is increasing. In addition, interferences are observable even when the distances between the ions is smaller than half a wavelength of the incident light.

quant-ph

Nanosecond Dynamics of Single-Molecule Fluorescence Resonance Energy Transfer

Motivated by recent experiments on photon statistics from individual dye pairs planted on biomolecules and coupled by fluorescence resonance energy transfer (FRET), we show here that the FRET dynamics can be modelled by Gaussian random processes with colored noise. Using Monte-Carlo numerical simulations, the photon intensity correlations from the FRET pairs are calculated, and are turned out to be very close to those observed in experiment. The proposed stochastic description of FRET is consistent with existing theories for microscopic dynamics of the biomolecule that carries the FRET coupled dye pairs.

quant-ph