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Subwavelength Localization of Atomic Excitation Using Electromagnetically Induced Transparency

J. A. Miles, Z. J. Simmons, and D. D. Yavuz
Phys. Rev. X 3, 031014 – Published 11 September 2013
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Abstract

We report an experiment in which an atomic excitation is localized to a spatial width that is a factor of 8 smaller than the wavelength of the incident light. The experiment utilizes the sensitivity of the dark state of electromagnetically induced transparency (EIT) to the intensity of the coupling laser beam. A standing-wave coupling laser with a sinusoidally varying intensity yields tightly confined Raman excitations during the EIT process. The excitations, located near the nodes of the intensity profile, have a width of 100 nm. The experiment is performed using ultracold Rb87 atoms trapped in an optical dipole trap, and atomic localization is achieved with EIT pulses that are approximately 100 ns long. To probe subwavelength atom localization, we have developed a technique that can measure the width of the atomic excitations with nanometer spatial resolution.

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  • Received 19 April 2013

DOI:https://doi.org/10.1103/PhysRevX.3.031014

This article is available under the terms of the Creative Commons Attribution 3.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI.

Published by the American Physical Society

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Localize and Conquer!

Published 11 September 2013

By illuminating atoms with two colors of light that drive interfering transitions, researchers selectively excite the atoms in a region much smaller than the light wavelength.

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Authors & Affiliations

J. A. Miles, Z. J. Simmons, and D. D. Yavuz

  • Department of Physics, 1150 University Avenue, University of Wisconsin at Madison, Madison, Wisconsin, 53706, USA

Popular Summary

Focusing light of a particular wavelength onto a spot smaller than half of the wavelength is fundamentally impossible because of the wave nature of light. This limit is called “the diffraction limit.” Using the light to “address” an atomic cloud of a size smaller than the diffraction limit would then be impossible for the same reason. In this experimental paper, we demonstrate that it is actually possible to overcome this limit to manipulate the internal states of atoms in a cloud smaller than the diffraction limit.

Our technique takes advantage of the structure of the internal states of our atoms, which are rubidium atoms. When unexcited, rubidium atoms stay in two ground states that differ only slightly in their energies. A laser beam of correct color can excite the atoms from one of the ground states to another state of much higher energy and thus becomes “absorbed” by the atoms. A very interesting phenomenon, the so-called electromagnetically induced transparency, is known to occur: When a second laser of a slightly different color (corresponding to the transition from the second ground state to the excited state) is added, the absorption of the first light is suppressed and a population transfer of the atoms from the first ground state to the second results.

The new physical insight behind our experiment is this: By manipulating when each laser is turned on and how powerful it is, we can control the population transfer of atoms between the two ground states, and how well this transfer is controlled spatially depends very sensitively on the ratio of the intensities of the two lasers—a quantity not subject to the diffraction limit. By appropriately engineering the ratio of the intensities, we have been able to achieve population transfer of atoms in “clouds” about one-eighth of the wavelength of the light used. Moreover, as direct “imaging” of such a subwavelength phenomenon is still prevented by the diffraction limit, we have devised a technique that can accurately determine the subwavelength size of the atomic cloud within which the population transfer takes place.

Our technique could lead to progress toward atomic manipulation and imaging with better spatial resolutions.

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Vol. 3, Iss. 3 — July - September 2013

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