12 results found
Scholl P, Williams HJ, Bornet G, et al., 2022, Microwave Engineering of Programmable XXZ Hamiltonians in Arrays of Rydberg Atoms, PRX Quantum, Vol: 3
We use the resonant dipole-dipole interaction between Rydberg atoms and a periodic external microwave field to engineer XXZ spin Hamiltonians with tunable anisotropies. The atoms are placed in one-dimensional (1D) and two-dimensional (2D) arrays of optical tweezers. As illustrations, we apply this engineering to two iconic situations in spin physics: the Heisenberg model in square arrays and spin transport in 1D. We first benchmark the Hamiltonian engineering for two atoms and then demonstrate the freezing of the magnetization on an initially magnetized 2D array. Finally, we explore the dynamics of 1D domain-wall systems with both periodic and open boundary conditions. We systematically compare our data with numerical simulations and assess the residual limitations of the technique as well as routes for improvement. The geometrical versatility of the platform, combined with the flexibility of the simulated Hamiltonians, opens up exciting prospects in the fields of quantum simulation, quantum information processing, and quantum sensing.
Williams HJ, 2022, Versatile neutral atoms take on quantum circuits., Nature, Vol: 604, Pages: 429-430
Scholl P, Schuler M, Williams HJ, et al., 2021, Quantum simulation of 2D antiferromagnets with hundreds of Rydberg atoms., Nature, Vol: 595, Pages: 233-238
Quantum simulation using synthetic systems is a promising route to solve outstanding quantum many-body problems in regimes where other approaches, including numerical ones, fail1. Many platforms are being developed towards this goal, in particular based on trapped ions2-4, superconducting circuits5-7, neutral atoms8-11 or molecules12,13. All of these platforms face two key challenges: scaling up the ensemble size while retaining high-quality control over the parameters, and validating the outputs for these large systems. Here we use programmable arrays of individual atoms trapped in optical tweezers, with interactions controlled by laser excitation to Rydberg states11, to implement an iconic many-body problem-the antiferromagnetic two-dimensional transverse-field Ising model. We push this platform to a regime with up to 196 atoms manipulated with high fidelity and probe the antiferromagnetic order by dynamically tuning the parameters of the Hamiltonian. We illustrate the versatility of our platform by exploring various system sizes on two qualitatively different geometries-square and triangular arrays. We obtain good agreement with numerical calculations up to a computationally feasible size (approximately 100 particles). This work demonstrates that our platform can be readily used to address open questions in many-body physics.
Jurgilas S, Chakraborty A, Rich CJH, et al., 2021, Collisions between Ultracold Molecules and Atoms in a Magnetic Trap, PHYSICAL REVIEW LETTERS, Vol: 126, ISSN: 0031-9007
Schymik KN, Lienhard V, Barredo D, et al., 2020, Enhanced atom-by-atom assembly of arbitrary tweezer arrays, Physical Review A, Vol: 102, ISSN: 2469-9926
We report on improvements extending the capabilities of the atom-by-atom assembler described by Barredo et al. [Science 354, 1021 (2016)SCIEAS0036-807510.1126/science.aah3778] that we use to create fully-loaded target arrays of more than 100 single atoms in optical tweezers, starting from randomly loaded, half-filled initial arrays. We describe four variants of the sorting algorithm that decrease the number of moves needed for assembly and enable the assembly of arbitrary, nonregular target arrays. We demonstrate experimentally the performance of this enhanced assembler for a variety of target arrays.
Caldwell L, Williams H, Fitch N, et al., 2020, Long rotational coherence times of molecules in a magnetic trap, Physical Review Letters, Vol: 124, ISSN: 0031-9007
Polar molecules in superpositions of rotational states exhibit long-range dipolar interactions, but maintaining their coherence in a trapped sample is a challenge. We present calculations that show many laser-coolable molecules have convenient rotational transitions that are exceptionally insensitive to magnetic fi elds. We verify this experimentally for CaF where we find a transition with sensitivity below 5 HzG‾¹ and use it to demonstrate a rotational coherence time of 6.4(8) ms in a magnetic trap. Simulations suggest it is feasible to extend this to > 1 s using a smaller cloud in abiased magnetic trap.
Caldwell L, Devlin J, Williams H, et al., 2019, Deep Laser Cooling and Efficient Magnetic Compression of Molecules, Physical Review Letters, Vol: 123, ISSN: 0031-9007
We introduce a scheme for deep laser cooling of molecules based on robust dark states at zero velocity. By simulating this scheme, we show it to be a widely applicable method that can reach the recoil limit or below. We demonstrate and characterise the method experimentally, reachinga temperature of 5.4(7) μK. We solve a general problem of measuring low temperatures for large clouds by rotating the phase-space distribution and then directly imaging the complete velocity distribution. Using the same phase-space rotation method, we rapidly compress the cloud. Applying the cooling method a second time, we compress both the position and velocity distributions.
Williams HJ, Caldwell L, Fitch NJ, et al., 2018, Magnetic trapping and coherent control of laser-cooled molecules, Physical Review Letters, Vol: 120, ISSN: 0031-9007
We demonstrate coherent microwave control of the rotational, hyperfine and Zeeman states of ultracold CaF molecules, and the magnetic trapping of these molecules in a single, selectable quantum state. We trap about 5 X 10³ molecules for almost 2s at a temperature of 70(8) μK and a density of 1.2 X 10⁵ cm⁻³. We measure the state-specific loss rate due to collisions with background helium.
The ability to cool atoms below the Doppler limit -- the minimum temperaturereachable by Doppler cooling -- has been essential to most experiments withquantum degenerate gases, optical lattices and atomic fountains, among manyother applications. A broad set of new applications await ultracold molecules,and the extension of laser cooling to molecules has begun. A molecularmagneto-optical trap has been demonstrated, where molecules approached theDoppler limit. However, the sub-Doppler temperatures required for mostapplications have not yet been reached. Here we cool molecules to 50 uK, wellbelow the Doppler limit, using a three-dimensional optical molasses. Theseultracold molecules could be loaded into optical tweezers to trap arbitraryarrays for quantum simulation, launched into a molecular fountain for testingfundamental physics, and used to study ultracold collisions and ultracoldchemistry.
Williams H, Truppe S, Hambach M, et al., 2017, Characteristics of a magneto-optical trap of molecules, New Journal of Physics, Vol: 19, ISSN: 1367-2630
We present the properties of a magneto-optical trap (MOT) of CaFmolecules. We study the process of loading the MOT from a decelerated bu er-gas-cooled beam, and how best to slow this molecular beam in order to capture the most molecules. We determine how the number of molecules, the photon scattering rate, the oscillation frequency, damping constant, temperature, cloud size and lifetime depend on the key parameters of the MOT, especially the intensity and detuning of the main cooling laser. We compare our results to analytical and numerical models, to the properties of standard atomic MOTs, and to MOTs of SrF molecules. We load up to 2 x 10⁴ molecules, and measure a maximum scattering rate of 2.5 x 10⁶ s⁻¹ per molecule, a maximum oscillation frequency of 100 Hz, a maximum damping constant of 500 s⁻¹, and a minimum MOT rms radius of 1.5 mm. A minimum temperature of 730 μK is obtained by ramping down the laser intensity to low values. The lifetime, typically about 100 ms, is consistent with a leak out of the cooling cycle with a branching ratio of about 6 x 10⁻⁶. The MOT has a capture velocity of about 11 m/s.
Truppe S, Williams HJ, Fitch NJ, et al., 2017, An intense, cold, velocity-controlled molecular beam by frequency-chirped laser slowing, NEW JOURNAL OF PHYSICS, Vol: 19, ISSN: 1367-2630
Using frequency-chirped radiation pressure slowing, we precisely control the velocity of a pulsed CaF molecular beam down to a few m s–1, compressing its velocity spread by a factor of 10 while retaining high intensity: at a velocity of 15 m s–1 the flux, measured 1.3 m from the source, is 7 × 105 molecules per cm2 per shot in a single rovibrational state. The beam is suitable for loading a magneto-optical trap or, when combined with transverse laser cooling, improving the precision of spectroscopic measurements that test fundamental physics. We compare the frequency-chirped slowing method with the more commonly used frequency-broadened slowing method.
Miralles V, Huerre A, Williams H, et al., 2015, A versatile technology for droplet-based microfluidics: thermomechanical actuation, LAB ON A CHIP, Vol: 15, Pages: 2133-2139, ISSN: 1473-0197
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