Prof Dieter Jaksch

Abstract:

Polar molecules offer a new platform for quantum simulation of systems with long-range interactions, based on the electrostatic interaction between their electric dipole moments. Here, we report the development of coherent quantum state control using microwave fields in $^{40}$Ca$^{19}$F and $^{87}$Rb$^{133}$Cs molecules, a crucial ingredient for many quantum simulation applications. We perform Ramsey interferometry measurements with fringe spacings of $\sim 1~\rm kHz$ and investigate the dephasing time of a superposition of $N=0$ and $N=1$ rotational states when the molecules are confined. For both molecules, we show that a judicious choice of molecular hyperfine states minimises the impact of spatially varying transition-frequency shifts across the trap. For magnetically trapped $^{40}$Ca$^{19}$F we use a magnetically insensitive transition and observe a coherence time of 0.61(3)~ms. For optically trapped $^{87}$Rb$^{133}$Cs we exploit an avoided crossing in the AC Stark shifts and observe a maximum coherence time of 0.75(6)~ms.

Abstract:

We show that strong parametric driving of a quantum harmonic oscillator coupled to a thermal bath allows one to distinguish between different microscopic models for the oscillator-bath coupling. We consider a bath with an Ohmic spectral density and a model where the system-bath interaction can be tuned continuously between position and momentum coupling via the coupling angle α. We derive a master equation for the reduced density operator of the oscillator in Born-Markov approximation and investigate its quasisteady state as a function of the driving parameters, the temperature of the bath and the coupling angle α. We find that the driving introduces a strong dependence of the time-averaged variance of position and momentum on these parameters. In particular, we identify parameter regimes that maximize the α dependence and provide an intuitive explanation of our results.

Abstract:

The $t$–$J$ model is a standard model of strongly correlated electrons, often studied in the context of high-$T_c$ superconductivity. However, most studies of this model neglect three-site terms, which appear at the same order as the superexchange $J$. As these terms correspond to pair-hopping, they are expected to play an important role in the physics of superconductivity when doped sufficiently far from half-filling. In this paper we present a density matrix renormalisation group study of the one-dimensional $t$–$J$ model with the pair hopping terms included. We demonstrate that these additional terms radically change the one-dimensional ground state phase diagram, extending the superconducting region at low fillings, while at larger fillings, superconductivity is completely suppressed. We explain this effect by introducing a simplified effective model of repulsive hardcore bosons.

Abstract:

We combine the multigrid (MG) method with state-of-the-art concepts from the variational formulation of the numerical renormalization group. The resulting MG renormalization (MGR) method is a natural generalization of the MG method for solving partial differential equations. When the solution on a grid of N points is sought, our MGR method has a computational cost scaling as O(log⁡(N)), as opposed to O(N) for the best standard MG method. Therefore MGR can exponentially speed up standard MG computations. To illustrate our method, we develop a novel algorithm for the ground state computation of the nonlinear Schrödinger equation. Our algorithm acts variationally on tensor products and updates the tensors one after another by solving a local nonlinear optimization problem. We compare several different methods for the nonlinear tensor update and find that the Newton method is the most efficient as well as precise. The combination of MGR with our nonlinear ground state algorithm produces accurate results for the nonlinear Schrödinger equation on N=1018grid points in three spatial dimensions.

Abstract:

We show that efficient norm-conserving pseudopotentials for electronic structure calculations can be obtained from a polynomial Ansatz for the potential. Our pseudopotential is a polynomial of degree ten in the radial variable and fulfils the same smoothness conditions imposed by the Troullier–Martins method (TM) (1991 Phys. Rev. B 43 1993) where pseudopotentials are represented by a polynomial of degree twenty-two. We compare our method to the TM approach in electronic structure calculations for diamond and iron in the bcc structure and find that the two methods perform equally well in calculations of the total energy. However, first and second derivatives of the total energy with respect to atomic coordinates converge significantly faster with the plane wave cutoff if the standard TM potentials are replaced by the pseudopotentials introduced here.