Stochastic thermodynamics as reviewed here systematically provides a framework for extending the notions of classical thermodynamics such as work, heat and entropy production to the level of individual trajectories of well-defined non-equilibrium ensembles. It applies whenever a non-equilibrium process is still coupled to one (or several) heat bath(s) of constant temperature. Paradigmatic systems are single colloidal particles in time-dependent laser traps, polymers in external flow, enzymes and molecular motors in single molecule assays, small biochemical networks and thermoelectric devices involving single electron transport. For such systems, a first-law like energy balance can be identified along fluctuating trajectories. For a basic Markovian dynamics implemented either on the continuum level with Langevin equations or on a discrete set of states as a master equation, thermodynamic consistency imposes a local-detailed balance constraint on noise and rates, respectively. Various integral and detailed fluctuation theorems, which are derived here in a unifying approach from one master theorem, constrain the probability distributions for work, heat and entropy production depending on the nature of the system and the choice of non-equilibrium conditions. For non-equilibrium steady states, particularly strong results hold like a generalized fluctuation–dissipation theorem involving entropy production. Ramifications and applications of these concepts include optimal driving between specified states in finite time, the role of measurement-based feedback processes and the relation between dissipation and irreversibility. Efficiency and, in particular, efficiency at maximum power can be discussed systematically beyond the linear response regime for two classes of molecular machines, isothermal ones such as molecular motors, and heat engines such as thermoelectric devices, using a common framework based on a cycle decomposition of entropy production. (Some figures may appear in colour only in the online journal) This article was invited by Erwin Frey.

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Stochastic thermodynamics, fluctuation theorems and molecular machines

Linear optics with photon counting is a prominent candidate for practical quantum computing. The protocol by Knill, Laflamme, and Milburn [2001, Nature (London) 409, 46] explicitly demonstrates that efficient scalable quantum computing with single photons, linear optical elements, and projective measurements is possible. Subsequently, several improvements on this protocol have started to bridge the gap between theoretical scalability and practical implementation. The original theory and its improvements are reviewed, and a few examples of experimental two-qubit gates are given. The use of realistic components, the errors they induce in the computation, and how these errors can be corrected is discussed.

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Linear optical quantum computing with photonic qubits

Quantum mechanics---the theory describing the fundamental workings of nature---is famously counterintuitive: it predicts that a particle can be in two places at the same time, and that two remote particles can be inextricably and instantaneously linked These predictions have been the topic of intense metaphysical debate ever since the theory's inception early last century However, supreme predictive power combined with direct experimental observation of some of these unusual phenomena leave little doubt as to its fundamental correctness In fact, without quantum mechanics we could not explain the workings of a laser, nor indeed how a fridge magnet operates Over the last several decades quantum information science has emerged to seek answers to the question: can we gain some advantage by storing, transmitting and processing information encoded in systems that exhibit these unique quantum properties? Today it is understood that the answer is yes Many research groups around the world are working towards one of the most ambitious goals humankind has ever embarked upon: a quantum computer that promises to exponentially improve computational power for particular tasks A number of physical systems, spanning much of modern physics, are being developed for this task---ranging from single particles of light to superconducting circuits---and it is not yet clear which, if any, will ultimately prove successful Here we describe the latest developments for each of the leading approaches and explain what the major challenges are for the future

Quantum Computing

"Quantum sensing" describes the use of a quantum system, quantum properties or quantum phenomena to perform a measurement of a physical quantity Historical examples of quantum sensors include magnetometers based on superconducting quantum interference devices and atomic vapors, or atomic clocks More recently, quantum sensing has become a distinct and rapidly growing branch of research within the area of quantum science and technology, with the most common platforms being spin qubits, trapped ions and flux qubits The field is expected to provide new opportunities - especially with regard to high sensitivity and precision - in applied physics and other areas of science In this review, we provide an introduction to the basic principles, methods and concepts of quantum sensing from the viewpoint of the interested experimentalist

Quantum sensing

Magnetic resonance imaging and optical microscopy are key technologies in the life sciences. For microbiological studies, especially of the inner workings of single cells, optical microscopy is normally used because it easily achieves resolution close to the optical wavelength. But in conventional microscopy, diffraction limits the resolution to about half the wavelength. Recently, it was shown that this limit can be partly overcome by nonlinear imaging techniques, but there is still a barrier to reaching the molecular scale. In contrast, in magnetic resonance imaging the spatial resolution is not determined by diffraction; rather, it is limited by magnetic field sensitivity, and so can in principle go well below the optical wavelength. The sensitivity of magnetic resonance imaging has recently been improved enough to image single cells, and magnetic resonance force microscopy has succeeded in detecting single electrons and small nuclear spin ensembles. However, this technique currently requires cryogenic temperatures, which limit most potential biological applications. Alternatively, single-electron spin states can be detected optically, even at room temperature in some systems. Here we show how magneto-optical spin detection can be used to determine the location of a spin associated with a single nitrogen-vacancy centre in diamond with nanometre resolution under ambient conditions. By placing these nitrogen-vacancy spins in functionalized diamond nanocrystals, biologically specific magnetofluorescent spin markers can be produced. Significantly, we show that this nanometre-scale resolution can be achieved without any probes located closer than typical cell dimensions. Furthermore, we demonstrate the use of a single diamond spin as a scanning probe magnetometer to map nanoscale magnetic field variations. The potential impact of single-spin imaging at room temperature is far-reaching. It could lead to the capability to probe biologically relevant spins in living cells.

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Nanoscale imaging magnetometry with diamond spins under ambient conditions

The fluorescence of individual nitrogen-vacancy defect centers in diamond was observed with room-temperature scanning confocal optical microscopy. The centers were photostable, showing no detectable change in their fluorescence emission spectrum as a function of time. Magnetic resonance on single centers at room temperature was shown to be feasible. The magnetic resonance spectra revealed marked changes in zero-field splitting parameters among different centers. These changes were attributed to strain-induced differences in the symmetry of the centers.

http://science.sciencemag.org/content/sci/276/5321/2012.full.pdf

Scanning confocal optical microscopy and magnetic resonance on single defect centers

Individual paramagnetic defect centers in diamond nanocrystals have been investigated by low-temperature high-resolution optical spectroscopy. Narrow fluorescence excitation spectral lines have been found, indicating transitions between individual spin sublevels. Spectral diffusion is explained by cross relaxation among spin sublevels and by the presence of excited electrons in the conduction band of diamond. The relaxation times are in the millisecond range. The system may be useful for quantum information processing with individual electron spins.

Single spin states in a defect center resolved by optical spectroscopy

A single defect center in diamond periodically excited by a laser is shown to provide a simple realization for a system obeying a fluctuation theorem for nonthermal noise. The distribution of these fluctuations is distinctly non-Gaussian, which has also been verified by numerical calculation. For driving protocols symmetric under time reversal a more restricted form of the theorem holds, which is also known from entropy fluctuations caused by thermal noise.

Experimental test of the fluctuation theorem for a driven two-level system with time-dependent rates.

Using fluorescence spectroscopy we directly measure entropy production of a single two-level system realized experimentally as an optically driven defect center in diamond. We exploit a recent suggestion to define entropy on the level of a single stochastic trajectory [Seifert, Phys. Rev. Lett. 95, 040602 (2005)10.1103/PhysRevLett.95.040602]. Entropy production can then be split into one of the system itself and one of the surrounding medium. We demonstrate that the total entropy production obeys various exact relations for finite time trajectories.

https://arxiv.org/pdf/cond-mat/0607407.pdf

Measurement of stochastic entropy production.

Individual nitrogen-vacancy defect centers have been investigated by low-temperature confocal microscopy and fluorescence excitation spectroscopy. At temperatures below 90 K the fluorescence intensity of individual centers drastically diminishes because of the population of a metastable singlet state in near resonance with the optically excited state. Low-temperature fluorescence excitation spectroscopy down to 5 K becomes possible via deshelving of this state with a second laser source. Surprisingly individual centers reveal low-temperature fluorescence excitation line widths around 0.6 meV, more than two orders of magnitude larger than expected from previous high resolution laser spectroscopy on bulk samples.

C. Tietz

Papers

Scanning confocal optical microscopy and magnetic resonance on single defect centers

Single spin states in a defect center resolved by optical spectroscopy

Experimental test of the fluctuation theorem for a driven two-level system with time-dependent rates.

Measurement of stochastic entropy production.

Low-temperature microscopy and spectroscopy on single defect centers in diamond