arXiv subjects

Janet Anders

Publications and source records attributed to Janet Anders.

At least 37 records · Page 2Linked to original sources

arXiv2024

Thermodynamically Optimal Protocols for Dual-Purpose Qubit Operations

Information processing, quantum or classical, relies on channels transforming multiple input states to different corresponding outputs. Previous research has established bounds on the thermodynamic resources required for such operations, but no protocols have been specified for their optimal implementation. For the insightful case of qubits, we here develop explicit protocols to transform two states in an energetically optimal manner. We first prove conditions on the feasibility of carrying out such transformations at all, and then quantify the achievable work extraction. Our results uncover a fundamental incompatibility between the thermodynamic ideal of slow, quasistatic processes and the information-theoretic requirement to preserve distinguishablity between different possible output states.

quant-ph↗

arXiv2024

Enhanced entanglement in multi-bath spin-boson models

The spin-boson model usually considers a spin coupled to a single bosonic bath. However, some physical situations require coupling of the spin to multiple environments. For example, spins interacting with phonons in three-dimensional magnetic materials. Here, we consider a spin coupled isotropically to three independent baths. We show that coupling to multiple baths can significantly increase entanglement between the spin and its environment at zero temperature. The effect of this is to reduce the spin's expectation values in the mean force equilibrium state. In contrast, the classical three-bath spin equilibrium state turns out to be entirely independent of the environmental coupling. These results reveal purely quantum effects that can arise from multi-bath couplings, with potential applications in a wide range of settings, such as magnetic materials.

quant-ph↗

arXiv2024

Accounting for Quantum Effects in Atomistic Spin Dynamics

Atomistic spin dynamics (ASD) is a standard tool to model the magnetization dynamics of a variety of materials. The fundamental dynamical model underlying ASD is entirely classical. In this paper, we present two approaches to effectively incorporate quantum effects into ASD simulations, thus enhancing their low temperature predictions. The first allows to simulate the magnetic behavior of a quantum spin system by solving the equations of motion of a classical spin system at an effective temperature relative to the critical temperature. This effective temperature is determined a priori from the microscopic properties of the system. The second approach is based on a \semi model where classical spins interact with an environment with a quantum-like power spectrum. The parameters that characterize this model can be calculated ab initio or extracted from experiments. This semi-classical model quantitatively reproduces the absolute temperature behavior of a magnetic system, thus accounting for the quantum mechanical aspects of its dynamics, even at low temperature. The methods presented here can be readily implemented in current ASD simulations with no additional complexity cost.

cond-mat.mtrl-sci↗

arXiv2024

Stability of long-sustained oscillations induced by electron tunneling

Self-oscillations are the result of an efficient mechanism generating periodic motion from a constant power source. In quantum devices, these oscillations may arise due to the interaction between single electron dynamics and mechanical motion. We show that, due to the complexity of this mechanism, these self-oscillations may irrupt, vanish, or exhibit a bistable behaviour causing hysteresis cycles. We observe these hysteresis cycles and characterize the stability of different regimes in both single and double quantum dot configurations. In particular cases, we find these oscillations stable for over 20 seconds, many orders of magnitude above electronic and mechanical characteristic timescales, revealing the robustness of the mechanism at play.

cond-mat.mes-hall↗

arXiv2024

Coupling a single spin to high-frequency motion

Coupling a single spin to high-frequency mechanical motion is a fundamental bottleneck of applications such as quantum sensing, intermediate and long-distance spin-spin coupling, and classical and quantum information processing. Previous experiments have only shown single spin coupling to low-frequency mechanical resonators, such as diamond cantilevers. High-frequency mechanical resonators, having the ability to access the quantum regime, open a range of possibilities when coupled to single spins, including readout and storage of quantum states. Here we report the first experimental demonstration of spin-mechanical coupling to a high-frequency resonator. We achieve this all-electrically on a fully suspended carbon nanotube device. A new mechanism gives rise to this coupling, which stems from spin-orbit coupling, and it is not mediated by strain. We observe both resonant and off-resonant coupling as a shift and broadening of the electric dipole spin resonance (EDSR), respectively. We develop a complete theoretical model taking into account the tensor form of the coupling and non-linearity in the motion. Our results propel spin-mechanical platforms to an uncharted regime. The interaction we reveal provides the full toolbox for promising applications ranging from the demonstration of macroscopic superpositions, to the operation of fully quantum engines, to quantum simulators.

cond-mat.mes-hall↗

arXiv2023

Long-time equilibration can determine transient thermality

When two initially thermal many-body systems start interacting strongly, their transient states quickly become non-Gibbsian, even if the systems eventually equilibrate. To see beyond this apparent lack of structure during the transient regime, we use a refined notion of thermality, which we call g-local. A system is g-locally thermal if the states of all its small subsystems are marginals of global thermal states. We numerically demonstrate for two harmonic lattices that whenever the total system equilibrates in the long run, each lattice remains g-locally thermal at all times, including the transient regime. This is true even when the lattices have long-range interactions within them. In all cases, we find that the equilibrium is described by the generalized Gibbs ensemble, with three-dimensional lattices requiring special treatment due to their extended set of conserved charges. We compare our findings with the well-known two-temperature model. While its standard form is not valid beyond weak coupling, we show that at strong coupling it can be partially salvaged by adopting the concept of a g-local temperature.

quant-ph↗

arXiv2023

Graph theory approach to exceptional points in wave scattering

In this paper, we use graph theory to solve wave scattering problems in the discrete dipole approximation. As a key result of this work, in the presence of active scatterers, we present a systematic method to find arbitrary large-order zero eigenvalue exceptional points (EPs). This is achieved by solving a set of non-linear equations that we interpret, in a graph theory picture, as vanishing sums of scattering events. We then show how the total field of the system responds to parameter perturbations at the EP. Finally, we investigate the sensitivity of the power output to imaginary perturbation in the design frequency. This perturbation can be employed to trade sensitivity for a different dissipation balance of the system. The purpose of the results of this paper is manifold. On the one hand, we aim to shed light on the link between graph theory and wave scattering. On the other hand, the results of this paper find application in all those settings where zero eigenvalue EPs play a unique role like in coherent perfect absorption (CPA) structures.

physics.optics↗

arXiv2023

Anisotropic signatures in the spin-boson model

Thermal equilibrium properties of nanoscale systems deviate from standard macroscopic predictions due to a non-negligible coupling to the environment. For anisotropic three-dimensional materials, we derive the mean force corrections to the equilibrium state of a classical spin vector. The result is valid at arbitrary coupling strength. Specifically, we consider cubic, orthorhombic, and monoclinic symmetries, and compare their spin expectation values as a function of temperature. We underpin the correctness of the mean force state by evidencing its match with the steady state of the simulated non-Markovian spin dynamics. The results show an explicit dependence on the symmetry of the confining material. In addition, some coupling symmetries show a spin alignment transition at zero temperature. Finally, we quantify the work extraction potential of the mean force-generated inhomogeneities in the energy shells. Such inhomogeneities constitute a classical equivalent to quantum coherences.

cond-mat.stat-mech↗

arXiv2022

Coupling function from bath density of states

Modelling of an open quantum system requires knowledge of parameters that specify how it couples to its environment. However, beyond relaxation rates, realistic parameters for specific environments and materials are rarely known. Here we present a method of inferring the coupling between a generic system and its bosonic (e.g., phononic) environment from the experimentally measurable density of states (DOS). With it we confirm that the DOS of the well-known Debye model for three-dimensional solids is physically equivalent to choosing an Ohmic bath. We further match a real phonon DOS to a series of Lorentzian coupling functions, allowing us to determine coupling parameters for gold, yttrium iron garnet (YIG) and iron as examples. The results illustrate how to obtain material-specific dynamical properties, such as memory kernels. The proposed method opens the door to more accurate modelling of relaxation dynamics, for example for phonon-dominated spin damping in magnetic materials.

quant-ph↗

arXiv2022

Quantum-classical correspondence in spin-boson equilibrium states at arbitrary coupling

The equilibrium properties of nanoscale systems can deviate significantly from standard thermodynamics due to their coupling to an environment. For the generalised $θ$-angled spin-boson model, we first derive a compact and general form of the classical equilibrium state including environmental corrections to all orders. Secondly, for the quantum spin-boson model we prove, by carefully taking a large spin limit, that Bohr's quantum-classical correspondence persists at all coupling strengths. This correspondence gives insight into the conditions for a coupled quantum spin to be well-approximated by a coupled classical spin-vector. Thirdly, we demonstrate that previously identified environment-induced 'coherences' in the equilibrium state of weakly coupled quantum spins, do not disappear in the classical case. Finally, we provide the first classification of the coupling parameter regimes for the spin-boson model, from weak to ultrastrong, both for the quantum case and the classical setting. Our results shed light on the interplay of quantum and mean force corrections in equilibrium states of the spin-boson model, and will help draw the quantum to classical boundary in a range of fields, such as magnetism and exciton dynamics.

quant-ph↗

arXiv2022

Ultrastrong coupling between electron tunneling and mechanical motion

The ultrastrong coupling of single-electron tunneling and nanomechanical motion opens exciting opportunities to explore fundamental questions and develop new platforms for quantum technologies. We have measured and modeled this electromechanical coupling in a fully-suspended carbon nanotube device and report a ratio of $g_\mathrm{m}/ω_\mathrm{m} = 2.72 \pm 0.14$, where $g_\mathrm{m}/2π= 0.80\pm 0.04$ GHz is the coupling strength and $ω_\mathrm{m}/2π=294.5$ MHz is the mechanical resonance frequency. This is well within the ultrastrong coupling regime and the highest among all other electromechanical platforms. We show that, although this regime was present in similar fully-suspended carbon nanotube devices, it went unnoticed. Even higher ratios could be achieved with improvement on device design.

cond-mat.mes-hall↗

arXiv2022

Optimal finite-time heat engines under constrained control

We optimize finite-time stochastic heat engines with a periodically scaled Hamiltonian under experimentally motivated constraints on the bath temperature $T$ and the scaling parameter $λ$. We present a general geometric proof that maximum-efficiency protocols for $T$ and $λ$ are piecewise constant, alternating between the maximum and minimum allowed values. When $λ$ is restricted to a small range and the system is close to equilibrium at the ends of the isotherms, a similar argument shows that this protocol also maximizes output power. These results are valid for arbitrary dynamics. We illustrate them for an overdamped Brownian heat engine, which can experimentally be realized using optical tweezers with stiffness $λ$.

cond-mat.stat-mech↗

arXiv2022

Thermodynamics and optimal protocols of multidimensional quadratic Brownian systems

We characterize finite-time thermodynamic processes of multidimensional quadratic overdamped systems. Analytic expressions are provided for heat, work, and dissipation for any evolution of the system covariance matrix. The Bures-Wasserstein metric between covariance matrices naturally emerges as the local quantifier of dissipation. General principles of how to apply these geometric tools to identify optimal protocols are discussed. Focusing on the relevant slow-driving limit, we show how these results can be used to analyze cases in which the experimental control over the system is partial.

cond-mat.stat-mech↗

arXiv2021

Cavity-Altered Thermal Isomerization Rates and Dynamical Resonant Localization in Vibro-Polaritonic Chemistry

It has been experimentally demonstrated that reaction rates for molecules embedded in microfluidic optical cavities are altered when compared to rates observed under "ordinary" reaction conditions. However, precise mechanisms of how strong coupling of an optical cavity mode to molecular vibrations affect the reactivity and how resonance behavior emerges are still under dispute. In the present work, we approach these mechanistic issues from the perspective of a thermal model reaction, the inversion of ammonia along the umbrella mode, in presence of a single cavity mode of varying frequency and coupling strength. A topological analysis of the related cavity Born-Oppenheimer potential energy surface in combination with quantum mechanical and transition state theory rate calculations reveals two quantum effects, leading to decelerated reaction rates in qualitative agreement with experiments: The stiffening of quantized modes perpendicular to the reaction path at the transition state, which reduces the number of thermally accessible reaction channels, and the broadening of the barrier region which attenuates tunneling. We find these two effects to be very robust in a fluctuating environment, causing statistical variations of potential parameters such as the barrier height. Further, by solving the time-dependent Schrödinger equation in the vibrational strong coupling regime, we identify a resonance behavior, in qualitative agreement with experimental and earlier theoretical work. The latter manifests as reduced reaction probability, when the cavity frequency $ω_c$ is tuned resonant to a molecular reactant frequency. We find this effect to be based on the dynamical localization of the vibro-polaritonic wavepacket in the reactant well.

quant-ph↗

arXiv2021

Global Quantum Thermometry

A paradigm shift in quantum thermometry is proposed. To date, thermometry has relied on local estimation, which is useful to reduce statistical fluctuations once the temperature is very well known. In order to estimate temperatures in cases where few measurement data or no substantial prior knowledge are available, we build instead a theory of global quantum thermometry. Based on scaling arguments, a mean logarithmic error is shown here to be the correct figure of merit for thermometry. Its full minimisation provides an operational and optimal rule to post-process measurements into a temperature reading, and it establishes a global precision limit. We apply these results to the simulated outcomes of measurements on a spin gas, finding that the local approach can lead to biased temperature estimates in cases where the global estimator converges to the true temperature. The global framework thus enables a reliable approach to data analysis in thermometry experiments.

quant-ph↗

arXiv2021

Comparing transient oligonucleotide hybridization kinetics using DNA-PAINT and optoplasmonic single-molecule sensing on gold nanorods

We report a comparison of two photonic techniques for single-molecule sensing: fluorescence nanoscopy and optoplasmonic sensing. As the test system, oligonucleotides with and without fluorescent labels are transiently hybridized to complementary docking strands attached to gold nanorods. Comparing the measured single-molecule kinetics helps to examine the influence of fluorescent labels as well as factors arising from different sensing geometries. Our results demonstrate that DNA dissociation is not significantly altered by the fluorescent label, while DNA association is affected by geometric factors in the two techniques. These findings open the door to exploiting plasmonic sensing and fluorescence nanoscopy in a complementary fashion, which will aid in building more powerful sensors and uncovering the intricate effects that influence the behavior of single molecules.

physics.optics↗

arXiv2021

Local master equations bypass the secular approximation

Master equations are a vital tool to model heat flow through nanoscale thermodynamic systems. Most practical devices are made up of interacting sub-system, and are often modelled using either local master equations (LMEs) or global master equations (GMEs). While the limiting cases in which either the LME or the GME breaks down are well understood, there exists a 'grey area' in which both equations capture steady-state heat currents reliably, but predict very different transient heat flows. In such cases, which one should we trust? Here, we show that, when it comes to dynamics, the local approach can be more reliable than the global one for weakly interacting open quantum systems. This is due to the fact that the secular approximation, which underpins the GME, can destroy key dynamical features. To illustrate this, we consider a minimal transport setup and show that its LME displays exceptional points (EPs). These singularities have been observed in a superconducting-circuit realisation of the model [1]. However, in stark contrast to experimental evidence, no EPs appear within the global approach. We then show that the EPs are a feature built into the Redfield equation, which is more accurate than the LME and the GME. Finally, we show that the local approach emerges as the weak-interaction limit of the Redfield equation, and that it entirely avoids the secular approximation.

quant-ph↗

arXiv2020

Gibbs mixing of partially distinguishable photons with a polarising beamsplitter membrane

For a thought experiment concerning the mixing of two classical gases, Gibbs concluded that the work that can be extracted from mixing is determined by whether or not the gases can be distinguished by a semi-permeable membrane; that is, the mixing work is a discontinuous function of how similar the gases are. Here we describe an optomechanical setup that generalises Gibbs' thought experiment to partially distinguishable quantum gases. Specifically, we model the interaction between a polarising beamsplitter, that plays the role of a semi-permeable membrane, and two photon gases of non-orthogonal polarisation. We find that the work arising from the mixing of the gases is related to the potential energy associated with the displacement of the microscopic membrane, and we derive a general quantum mixing work expression, valid for any two photon gases with the same number distribution. The quantum mixing work is found to change continuously with the distinguishability of the two polarised gases. In addition, fluctuations of the work on the microscopic membrane become important, which we calculate for Fock and thermal states of the photon gases. Our findings generalise Gibbs' mixing to the quantum regime and open the door for new quantum thermodynamic (thought) experiments with quantum gases with non-orthogonal polarisations and microscopic pistons that can distinguish orthogonal polarisations.

quant-ph↗