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arXiv:1208.3268 · Journal of the Optical Society of America B

Impact of decoherence on internal state cooling using optical frequency combs

Svetlana Malinovskaya, Stephen L. Horton

Published Feb 8, 2013• 7 citations
arXivHTMLPDF

Abstract

We discuss femtosecond Raman-type techniques to control molecular vibrations, which can be implemented for internal-state cooling from Feshbach states with the use of optical frequency combs (OFCs) with and without modulation. The technique makes use of multiple two-photon resonances induced by optical frequencies present in the comb. It provides us with a useful tool to study the details of molecular dynamics at ultracold temperatures. In our theoretical model we take into account decoherence in the form of spontaneous emission and collisional dephasing in order to ascertain an accurate model of the population transfer in the three-level system. We analyze the effects of odd and even chirps of the OFC in the form of sine and cosine functions on the population transfer. We compare the effects of these chirps to the results attained with the standard OFC to see if they increase the population transfer to the final deeply bound state in the presence of decoherence. We also analyze the inherent phase relation that takes place owing to collisional dephasing between molecules in each of the states. This ability to control the rovibrational states of a molecule with an OFC enables us to create deeply bound ultra-cold polar molecules from the Feshbach state.

DOI
10.1364/josab.30.000482

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We discuss femtosecond Raman-type techniques to control molecular vibrations, which can be implemented for internal-state cooling from Feshbach states with the use of optical frequency combs (OFCs) with and without modulation. The technique makes use of multiple two-photon resonances induced by optical frequencies present in the comb. It provides us with a useful tool to study the details of molecular dynamics at ultracold temperatures. In our theoretical model we take into account decoherence in the form of spontaneous emission and collisional dephasing in order to ascertain an accurate model of the population transfer in the three-level system. We analyze the effects of odd and even chirps of the OFC in the form of sine and cosine functions on the population transfer. We compare the effects of these chirps to the results attained with the standard OFC to see if they increase the population transfer to the final deeply bound state in the presence of decoherence. We also analyze the inherent phase relation that takes place owing to collisional dephasing between molecules in each of the states. This ability to control the rovibrational states of a molecule with an OFC enables us to create deeply bound ultra-cold polar molecules from the Feshbach state.
We show that a single femtosecond optical frequency comb may be used to induce two-photon transitions between molecular vibrational levels to form ultracold molecules (e.g., KRb). The phase across an individual pulse in the pulse train is sinusoidally modulated with a carefully chosen modulation amplitude and frequency. Piecewise adiabatic population transfer is fulfilled to the final state by each pulse in the applied pulse train, providing a controlled population accumulation in the final state. Detuning the pulse train carrier and modulation frequency from one-photon resonances changes the time scale of molecular dynamics but leads to the same complete population transfer to the ultracold state. A standard optical frequency comb with no modulation is shown to induce similar dynamics, leading to rovibrational cooling.
We report on a theoretical study of implementation of a single femtosecond optical frequency comb to perform an efficient transfer of Feshbach molecules to the ground electronic and rovibrational state. A standard optical frequency comb is considered with zero offset frequency and a sinusoidally phase modulated frequency comb, having modulation frequency in the IR region. A stepwise population transfer to the ultracold molecular state is observed, with a negligible population of the excited state in the case of the sinusoidally modulated frequency comb.
Abstract A single femtosecond optical frequency comb is implemented to induce two‐photon transitions between molecular vibrational levels to form ultracold molecules. The phase across an individual pulse in the pulse train is sinusoidally modulated with a carefully chosen modulation amplitude and frequency. Piecewise population transfer is fulfilled to the final state by each pulse in the applied pulse train providing a controlled population accumulation in the final, ultracold state. The dynamics of rovibrational cooling is discussed on an example of the KRb molecule. © 2010 Wiley Periodicals, Inc. Int J Quantum Chem, 2010
Abstract Based on the proposed theoretical model of a three-level system, the optical Bloch equations including the direct two-photon transition (DTPT) process using the optical frequency comb (OFC) were derived and the population distribution of particles in the upper states varying with the velocity of the atoms was obtained. Comparing to the resonance two-photon transition process, that population was increased by a factor of 1.4 without the Doppler shift, which is consistent with our previous experimental results. Simultaneously, the relationships between momentum transfers, and atomic velocity and pulse number were analyzed. When applied to a multi-level system it was found that the population of particles in the excited states increased by a few percentages. The novel approach of DTPT using OFC improved the utilization of comb teeth and atoms, increased the momentum transfer path, reduced the reachable Doppler temperature limit, and encouraged us to use OFC to cool multiple elements simultaneously through the DTPT process. By analyzing the Doppler temperature of 133 Cs and 87 Rb in one dimension, it was found that this process can lower a temperature below 100 mK and generate dipolar molecules 133 Cs 87 Rb via photoassociation, which provides us with a new tool to create dipolar molecules and to investigate their complex rovibrational spectra in ultra-cold chemistry.
AbstractA method is proposed to create molecules in the ultracold state from the Feshbach molecules by stepwise adiabatic passage using an optical frequency comb without losses due to decoherence. An emphasis is made on the impact of the vibrational state manifold on controllability of the coherent dynamics by including five excited states into the model. The results are compared with recently reported results on a three-level λ system. Sinusoidal modulation across an individual pulse in the pulse train is applied, leading to the creation of a quasi-dark state, which minimizes population of the transitional, vibrational state manifold, and efficiently mitigates decoherence in the system. The parity of the temporal chirp is shown to be an important factor in designing population dynamics in the system.