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Julian Feß

Publications and source records attributed to Julian Feß.

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Enhancing the power of a quantum heat engine via control of the system--reservoir coupling

The non-equilibrium properties of open quantum systems are determined by the microscopic laws governing energy exchange with their environment. In particular, an enhancement of the performance of quantum heat engines has been predicted by speeding up the dynamics through control of the system--bath interaction. However, direct microscopic control of heat transfer between the machine and the reservoir has remained elusive so far. Here, we experimentally demonstrate such control in a quantum Otto engine realized with ultracold Cs-133 atoms coupled to an atomic reservoir of ultracold Rb-87 atoms. Heat exchange between the two is mediated by inelastic s-wave collisions whose energy-dependent scattering cross sections lead to an asymmetric equilibration dynamics in the isochoric heating and cooling strokes. By tuning the kinetic temperature of the atomic reservoir, we modify the associated microscopic scattering rates, and thereby the heat transfer law, giving control over the time allocation within the engine cycle through control over the microscopic, multi-exponential relaxation dynamics. This enables power output optimization at fixed efficiency. Our results establish microscopic control of system-reservoir interactions as a tool for manipulating heat flow at the nanoscale and engineering the finite-time performance of quantum thermal machines.

quant-ph

Quantum-enabled active matter at the atomic scale

Active matter comprises particles that extract energy from their local environment and convert it into motion. Although active particles have been miniaturized down to the nanoscale, realizing activity at the fundamentally smaller scale of individual atoms remains an open challenge, where quantum effects become increasingly relevant. Here, we experimentally demonstrate that individual Cs-133 atoms confined in an optical dipole trap extract energy from an ultracold bath of Rb-87 atoms via quantum-mechanical spin interactions and convert it into active motion. We quantitatively reproduce the resulting dynamics using a parameter-free active Langevin model derived from kinetic theory and support it with event-driven Monte Carlo collision simulations. The microscopic origin of activity is identified as quantum spin exchange, which transfers discrete internal spin energy into kinetic motion. Our work establishes a quantum-enabled route to active matter at the fundamental size limit of single atoms and opens perspectives for exploring the interplay of activity, quantum physics, and mesoscopic non-equilibrium thermodynamics.

quant-ph

Indication of critical scaling in time during the relaxation of an open quantum system

Phase transitions correspond to the singular behavior of physical systems in response to continuous control parameters like temperature or external fields. Near continuous phase transitions, associated with the divergence of a correlation length, universal power-law scaling behavior with critical exponents independent of microscopic system details is found. Recently, dynamical quantum phase transitions and universal scaling have been predicted and also observed in the non-equilibrium dynamics of isolated quantum systems after a quench, with time playing the role of the control parameter. However, signatures of such critical phenomena in time in open systems, whose dynamics is driven by the dissipative contact to an environment, were so far elusive. Here, we present results indicating that critical scaling with respect to time can also occur during the relaxation dynamics of an open quantum system described by mixed states. We experimentally measure the relaxation dynamics of the large atomic spin of individual Caesium atoms induced by the dissipative coupling via spin-exchange processes to an ultracold Bose gas of Rubidium atoms. For initial states far from equilibrium, the entropy of the spin state is found to peak in time, transiently approaching its maximum possible value, before eventually relaxing to its lower equilibrium value. Moreover, a finite-size scaling analysis based on numerical simulations shows that it corresponds to a critical point with respect to time of the dissipative system in the limit of large system sizes. It is signalled by the divergence of a characteristic length at a critical time, characterized by critical exponents that are found to be independent of system details.

cond-mat.quant-gas

Measuring the environment of a Cs qubit with dynamical decoupling sequences

We report the experimental implementation of dynamical decoupling on a small, non-interacting ensemble of up to 25 optically trapped, neutral Cs atoms. The qubit consists of the two magnetic-insensitive Cs clock states $\left| F=3, m_F=0 \right>$ and $\left|F=4, m_F=0\right>$, which are coupled by microwave radiation. We observe a significant enhancement of the coherence time when employing Carr-Purcell-Meiboom-Gill (CPMG) dynamical decoupling. A CPMG sequence with ten refocusing pulses increases the coherence time of 16.2(9) ms by more than one order of magnitude to 178(2) ms. In addition, we make use of the filter function formalism and utilize the CPMG sequence to measure the background noise floor affecting the qubit coherence, finding a power-law noise spectrum $1/ω^α$ with $\mathitα = 0.89(2)$. This finding is in very good agreement with an independent measurement of the noise in the intensity of the trapping laser. Moreover, the measured coherence evolutions also exhibit signatures of low-frequency noise originating at distinct frequencies. Our findings point toward noise spectroscopy of engineered atomic baths through single-atom dynamical decoupling in a system of individual Cs impurities immersed in an ultracold $^{87}$Rb bath.

quant-ph