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arXiv:physics/0512065 · Physical Review A

Laser cooling of atoms and molecules with ultrafast pulses

D. Kielpinski

Published Jun 13, 2006• 67 citations
arXivHTMLPDF

Abstract

We propose a laser cooling method for atomic species whose level structure makes traditional laser cooling difficult. For instance, laser cooling of hydrogen requires single-frequency vacuum-ultraviolet light, while multielectron atoms need single-frequency light at many widely separated frequencies. These restrictions can be eased by laser cooling on two-photon transitions with ultrafast pulse trains. Laser cooling of hydrogen, antihydrogen, and many other species appears feasible, and extension of the technique to molecules may be possible.

DOI
10.1103/physreva.73.063407

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We propose a laser cooling method for atomic species whose level structure makes traditional laser cooling difficult. For instance, laser cooling of hydrogen requires single-frequency vacuum-ultraviolet light, while multielectron atoms need single-frequency light at many widely separated frequencies. These restrictions can be eased by laser cooling on two-photon transitions with ultrafast pulse trains. Laser cooling of hydrogen, antihydrogen, and many other species appears feasible, and extension of the technique to molecules may be possible.
Despite the prominent role of laser cooling in modern atomic physics, with applications ranging from quantum sensors to high-precision spectroscopy and ultracold chemistry, laser cooling techniques are still limited to atoms with simple energy level structure and closed transitions that are accessible by currently available continuous wave (cw) laser sources. Two main obstacles prevent the extension of laser cooling techniques to a variety of atomic species and molecules. The first is associated with technical difficulties in creating cw laser light in the vacuum ultraviolet (VUV) spectral range - the absence of those laser sources prevents laser cooling of simple atoms such as hydrogen, deuterium, and antihydrogen. The second obstacle is associated with complex energy level structure of many atoms and almost all molecules - it permits decay of an excited state into a number of lower-lying states that can be widely separated in energy, which makes laser cooling of such species inefficient and experimentally very challenging.
Recently, laser cooling methods have been extended from atoms to molecules. The complex rotational and vibrational energy level structure of molecules makes laser cooling difficult, but these difficulties have been overcome and molecules have now been cooled to a few microkelvin and trapped for several seconds. This opens many possibilities for applications in quantum science and technology, controlled chemistry, and tests of fundamental physics. This article explains how molecules can be decelerated, cooled and trapped using laser light, reviews the progress made in recent years, and outlines some future applications.
We propose to extend coherent laser cooling from narrowband to broadband transitions by using trains of ultrashort broadband pulses. We analytically study two possible methods to reduce the momentum spread of a distribution by several units of photon momentum in a single spontaneous emission lifetime. We report on numerical simulations of one-dimensional laser cooling of a two-level system with realistic parameters. With this scheme, coherent laser cooling can in particular be implemented in the case of fast species with a short lifetime such as positronium.
Ultracold atoms, produced by laser cooling and trapping, have led to recent advances in quantum information, quantum chemistry, and quantum sensors.A lack of ultraviolet narrow-band lasers precludes laser cooling of prevalent atoms such as hydrogen, carbon, oxygen, and nitrogen.Broadband pulsed lasers can produce high power in the ultraviolet, and we demonstrate that the entire spectrum of an optical frequency comb can cool atoms when used to drive a narrow two-photon transition.This multiphoton optical force is also used to make a magneto-optical trap.These techniques may provide a route to ultracold samples of nature's most abundant building blocks for studies of pure-state chemistry and precision measurement.
Ultracold molecular gases are promising as an avenue to rich many-body physics, quantum chemistry, quantum information, and precision measurements. This richness, which flows from the complex internal structure of molecules, makes the creation of ultracold molecular gases using traditional methods (laser plus evaporative cooling) a challenge, in particular due to the spontaneous decay of molecules into dark states. We propose a way to circumvent this key bottleneck using an all-optical method for decelerating molecules using stimulated absorption and emission with a single ultrafast laser. We further describe single-photon cooling of the decelerating molecules that exploits their high dark state pumping rates, turning the principal obstacle to molecular laser cooling into an advantage. Cooling and deceleration may be applied simultaneously and continuously to load molecules into a trap. We discuss implementation details including multilevel numerical simulations of strontium monohydride. These techniques are applicable to a large number of molecular species and atoms with the only requirement being an electric dipole transition that can be accessed with an ultrafast laser.
To laser-cool a species, a closed (or nearly closed) cycle is required to dissipate translational energy through many directed laser-photon absorption and subsequent randomly-directed spontaneous emission events. Many atoms lend themselves to such a closed-loop cooling cycle. Attaining laser-cooled molecular species is challenging because of their inherently complex internal structure, yet laser-cooling molecules could lead to studies in interesting chemical dynamics among other applications. Typically, laser-cooled atoms are assembled into molecules through photoassociation or Feschbach resonance. CaH is one of a few molecules whose internal structure is quite atom-like, allowing a nearly closed cycle without the need for many repumping lasers. We will also present our work-to-date on laser cooling this molecule. We employ traditional pulsed atomic/molecular beam techniques with a laser vaporization source to generate species with well-defined translational energies over a narrow range of velocity. In this way, we can apply laser-cooling to most species in the beam along a single dimension (the beam’s axis). This project is funded by the LDRD program of the Los Alamos National Laboratory.