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.
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.
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.
We report on laser cooling of neutral rubidium atoms by using a single mode of a frequency comb. Cooling is achieved on a dipole-allowed transition at 780 nm in a one-dimensional retro-reflected beam geometry. Temperatures are measured using standard time-of-flight imaging. We show the dependence of the temperature on the cooling time, intensity and detuning of the frequency comb. The lowest temperature achieved is approximately equal to the Doppler temperature and is limited by the intensity of the comb mode driving the cooling transition. Additionally, we verify the analogy between frequency comb and continuous-wave laser cooling. Our work is a step towards laser cooling of atoms with strong cycling transitions in the vacuum ultraviolet, such as hydrogen, deuterium and antihydrogen, where generation of continuous-wave laser light is limited by current laser technology. Achieving efficient cooling at these wavelengths would significantly improve the precision of optical frequency standards, enable measurements of fundamental constants with unprecedented accuracy, improve tests of charge, parity, and time reversal symmetry, and open the way to achieving quantum degeneracy width new atomic species.
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.
Cold and ultracold molecules are highly desirable for a diverse range of applications in physics and chemistry such as precision measurements, tests of fundamental physics, quantum simulation and information processing, quantum chemistry, and the physics of strongly correlated quantum matter. Laser cooling is usually infeasible in molecules because their rotational and vibrational transitions make is difficult to come up with a closed scattering cycle. Recently, a narrow range of diatomic molecules, one of which is CaF, has been shown to possess a convenient electronic structure and a highly-diagonal Franck-Condon matrix and thus be amenable to laser cooling. This thesis describes experiments on laser cooling of CaF radicals produced in a supersonic source. We first investigate the increased fluorescence when multi-frequency resonant light excites the molecules from the four hyperfine levels of the ground X²∑+(N = 1, v = 0) state to the first excited A²π½ (J’ = 1=2; v’ = 0) state. The number of photons scattered per molecule increases significantly from one or two in the single frequency case to more than 50 before the molecules get pumped into the X²∑+(N = 1; v = 1) state. We demonstrate laser cooling and slowing of CaF using counter-propagating laser light which causes the molecules to scatter more than a thousand photons on the X (N = 1, v = 0, 1) <->A (J’ = 1=2; v’ = 0) transition. The effect of the laser cooling is to slow a group of molecules from 600 ms-1 to about 580 ms-1 and to narrow their velocity distribution from an initial temperature of 3 K down to 300 mK. In addition, chirping the frequency of the cooling light to keep it on resonance with the decelerating molecules doubles the deceleration and further compresses the velocity distribution. The effect of the laser cooling is limited by the optical pumping of molecules in the X (N = 1, v = 2) state.
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.
Slowing, cooling, and trapping molecules One of the major achievements in physics during the last two decades of the twentieth century was the ability to cool and trap atoms [1]. Laser cooling can produce previously inconceivable atomic temperatures of less than 1 μK. Atoms with sufficiently low kinetic energy can be trapped in magnetic and optical traps and thus studied for a prolonged time, thereby improving the resolution of spectroscopy by many orders of magnitude as well as reducing Doppler broadening. Furthermore, besides the external degrees of freedom, the internal degrees of freedom of the atoms can also be manipulated, leading to full control of the atoms. One of the holy grails of physics, the achievement of Bose–Einstein condensation in a dilute gas, was achieved mainly because of laser cooling and trapping of atoms. One of the natural extensions of laser cooling and trapping of atoms is the application of the techniques to molecules. Molecules offer a much richer internal structure than atoms, and thus provide extended possibilities to experimentalists. However, atomic laser cooling is based on the repetitive scattering of light and requires a closed, or at least nearly closed, two-level system. Because of the complicated internal structure of molecules, a closed two-level system cannot usually be found because they have many different electronic, vibrational, and rotational states and in general can decay to many different states after absorption of light (see Chap. 16). This requires a complete rethinking of the schemes that are used to cool atoms. Still, because of the extended possibilities cold molecules can offer with respect to cold atoms, there have been a large number of techniques developed to slow, cool, and trap them. These techniques can be divided into two classes, namely direct and indirect cooling. In the first case, molecules at cryogenic or room temperature are directly slowed and cooled. Although many different slowing techniques are used, this chapter focuses on Stark slowing of molecules since it was the first technique developed. Apart from the Stark shift of the molecules, the Zeeman and light shift of molecules can also be used to slow them. The idea behind Stark slowing is to subject the moving molecules to a continuously increasing electric field so that their kinetic energy is converted into potential energy.