RESUMO
We report laser cooling and trapping of yttrium monoxide molecules in an optical lattice. We show that gray molasses cooling remains exceptionally efficient for yttrium monoxide molecules inside the lattice with a molecule temperature as low as 6.1(6) µK. This approach has produced a trapped sample of 1200 molecules, with a peak spatial density of â¼1.2×10^{10} cm^{-3}, and a peak phase-space density of â¼3.1×10^{-6}. By ramping down the lattice depth, we cool the molecules further to 1.0(2) µK, 20 times colder than previously reported for laser-cooled molecules in a trap.
RESUMO
Benchmark relativistic coupled-cluster calculations for yttrium monoxide (YO) with accurate treatment of relativistic and electron correlation effects are reported. The spin-orbit mixing of 2Π and 2Δ is found to be an order of magnitude smaller than previously reported in the literature. Together with the measurement of the lifetime of the A'2Δ3/2 state, it implies an enhanced capability of a narrow-line cooling scheme to bring YO to sub-recoil temperature. The computed electronic transition properties also support a four-photon scheme to close the leakage of the A2Π1/2 â X2Σ1/2+ cycle through the A'2Δ3/2 state by repumping the A'2Δ3/2 state to the B2Σ1/2+ state, which subsequently decays back to X2Σ1/2+. Relativistic coupled-cluster methods, capable of providing accurate spectroscopic parameters that characterize the local potential curves and hence of providing accurate Franck-Condon factors, appear to be promising candidates for accurate calculation of properties for laser-coolable molecules.
RESUMO
Complex molecular structure demands customized solutions to laser cooling by extending its general set of principles and practices. Compared with other laser-cooled molecules, yttrium monoxide (YO) exhibits a large electron-nucleus interaction, resulting in a dominant hyperfine interaction over the electron spin-rotation coupling. The YO ground state is thus comprised of two manifolds of closely spaced states, with one of them possessing a negligible Landé g factor. This unique energy level structure favors dual-frequency dc magneto-optical trapping (MOT) and gray molasses cooling (GMC). We report exceptionally robust cooling of YO at 4 µK over a wide range of laser intensity, detunings (one- and two-photon), and magnetic field. The magnetic insensitivity enables the spatial compression of the molecular cloud by alternating GMC and MOT under the continuous operation of the quadrupole magnetic field. A combination of these techniques produces a laser-cooled molecular sample with the highest phase space density in free space.
RESUMO
In recent years substantial efforts have been expended in extending thermodynamics to single quantum systems. Quantum effects have emerged as a resource that can improve the performance of heat machines. However in the fully quantum regime their implementation still remains a challenge. Here, we report an experimental realization of a quantum absorption refrigerator in a system of three trapped ions, with three of its normal modes of motion coupled by a trilinear Hamiltonian such that heat transfer between two modes refrigerates the third. We investigate the dynamics and steady-state properties of the refrigerator and compare its cooling capability when only thermal states are involved to the case when squeezing is employed as a quantum resource. We also study the performance of such a refrigerator in the single shot regime made possible by coherence and demonstrate cooling below both the steady-state energy and a benchmark set by classical thermodynamics.
RESUMO
We report three-dimensional trapping of an oxide molecule (YO), using a radio-frequency magneto-optical trap (MOT). The total number of molecules trapped is â¼1.5×10^{4}, with a temperature of 4.1(5) mK. This diversifies the frontier of molecules that are laser coolable and paves the way for the second-stage narrow-line cooling in this molecule to the microkelvin regime. Futhermore, the new challenges of creating a 3D MOT of YO resolved here indicate that MOTs of more complex nonlinear molecules should be feasible as well.
RESUMO
Interaction among harmonic oscillators described by a trilinear Hamiltonian âξ(a^{}bc+ab^{}c^{}) is one of the most fundamental models in quantum optics. By employing the anharmonicity of the Coulomb potential in a linear trapped three-ion crystal, we experimentally implement it among three normal modes of motion in the strong-coupling regime, where the coupling strength is much larger than the decoherence rate of the ion motion. We use it to simulate the interaction of an atom and light as described by the Tavis-Cummings model and the process of nondegenerate parametric down-conversion in the regime of a depleted pump.
RESUMO
State measurement of a quantum harmonic oscillator is essential in quantum optics and quantum information processing. In a system of trapped ions, we experimentally demonstrate the projective measurement of the state of the ions' motional mode via an effective cross-Kerr coupling to another motional mode. This coupling is induced by the intrinsic nonlinearity of the Coulomb interaction between the ions. We spectroscopically resolve the frequency shift of the motional sideband of the first mode due to the presence of single phonons in the second mode and use it to reconstruct the phonon number distribution of the second mode.
RESUMO
A strong nonlinear coupling between harmonic oscillators is highly desirable for quantum information processing and quantum simulation, but is difficult to achieve in many physical systems. Here, we exploit the Coulomb interaction between two trapped ions to achieve strong nonlinear coupling between normal modes of motion at the single-phonon level. We experimentally demonstrate phonon up- and down-conversion and apply this coupling to directly measure the parity and Wigner functions of the ions' motional states. Our results represent the fully quantum operation of a degenerate parametric oscillator and hold promise for quantum computation schemes that involve continuous variables.
RESUMO
We experimentally demonstrate microwave control of the motional state of a trapped ion placed in a state-dependent potential generated by a running optical lattice. Both the optical lattice depth and the running lattice frequency provide tunability of the spin-motion coupling strength. The spin-motional coupling is exploited to demonstrate sideband cooling of a ^{171}Yb^{+} ion to the ground state of motion.