Directional amplification with a Josephson circuit

Non-reciprocal devices, which have different transmission coefficients for propagating waves in opposite directions, are crucial components in many low noise quantum measurements. In most schemes, magneto-optical effects provide the necessary non-reciprocity. In contrast, the proof-of-principle device presented here, consists of two on-chip coupled Josephson parametric converters (JPCs), which achieves directionality by exploiting the non-reciprocal phase response of the JPC in the trans-gain mode. The non-reciprocity of the device is controlled in-situ by varying the amplitude and phase difference of two independent microwave pump tones feeding the system. At the desired working point and for a signal frequency of 8.453 GHz, the device achieves a forward power gain of 15 dB within a dynamical bandwidth of 9 MHz, a reverse gain of -6 dB and suppression of the reflected signal by 8 dB. We also find that the amplifier adds a noise equivalent to less than one and a half photons at the signal frequency (referred to the input). It can process up to 3 photons at the signal frequency per inverse dynamical bandwidth. With a directional amplifier operating along the principles of this device, qubit and readout preamplifier could be integrated on the same chip.Comment: 7 pages, 5 figure

Inactivation of mitochondrial aspartate aminotransferase contributes to the respiratory deficit of yeast frataxin-deficient cells

International audienceFriedreich's ataxia is a hereditary neurodegenerative disease caused by reduced expression of mitochondrial frataxin. Frataxin deficiency causes impairment in respiratory capacity, disruption of iron homoeostasis and hypersensitivity to oxidants. Although the redox properties of NAD (NAD + and NADH) are essential for energy metabolism, only few results are available concerning homoeostasis of these nucleotides in frataxin-deficient cells. In the present study, we show that the malate-aspartate NADH shuttle is impaired in Saccharomyces cerevisiae frataxin-deficient cells (yfh1) due to decreased activity of cytosolic and mitochondrial isoforms of malate dehydrogenase and to complete inactivation of the mitochondrial aspartate aminotransferase (Aat1). A considerable decrease in the amount of mitochondrial acetylated proteins was observed in the yfh1 mutant compared with wild-type. Aat1 is acetylated in wild-type mitochondria and deacetylated in yfh1 mitochondria suggesting that inactivation could be due to this post-translational modification. Mutants deficient in iron-sulfur cluster assembly or lacking mitochondrial DNA also showed decreased activity of Aat1, suggesting that Aat1 inactivation was a secondary phenotype in yfh1 cells. Interestingly, deletion of the AAT1 gene in a wild-type strain caused respiratory deficiency and disruption of iron homoeostasis without any sensitivity to oxidative stress. Our results show that secondary inactivation of Aat1 contributes to the amplification of the respiratory defect observed in yfh1 cells. Further implication of mitochondrial protein deacetylation in the physiology of frataxin-deficient cells is anticipated

Comparing and combining measurement-based and driven-dissipative entanglement stabilization

We demonstrate and contrast two approaches to the stabilization of qubit entanglement by feedback. Our demonstration is built on a feedback platform consisting of two superconducting qubits coupled to a cavity which are measured by a nearly-quantum-limited measurement chain and controlled by high-speed classical logic circuits. This platform is used to stabilize entanglement by two nominally distinct schemes: a "passive" reservoir engineering method and an "active" correction based on conditional parity measurements. In view of the instrumental roles that these two feedback paradigms play in quantum error-correction and quantum control, we directly compare them on the same experimental setup. Further, we show that a second layer of feedback can be added to each of these schemes, which heralds the presence of a high-fidelity entangled state in realtime. This "nested" feedback brings about a marked entanglement fidelity improvement without sacrificing success probability.Comment: 40 pages, 12 figure

Size-Dependent Optical Properties of Dendronized Perylenediimide Nanoparticle Prepared by Laser Ablation in Water

Fluorescent nanoparticles of dendronized perylenediimide (DPDI) were fabricated by laser ablation in water. We succeeded in the preparation of colloidal nanoparticles of different sizes (150–400 nm) and examined their size-dependent optical absorption and fluorescence properties. The size-dependent extinction spectra can be explained by the effect of light scattering loss, and it was confirmed that their absorption spectrum is similar to that of molecules in solution. The very weak interchromophoric interaction is also confirmed by fluorescence spectral measurement. On the other hand, we found that the fluorescence quantum yield decreases with decreasing of the particle size, and we propose a new mechanism for the size-dependent reduction of emission intensity in organic nanoparticles. On the basis of the size dependent-fluorescence quantum yield and solvent polarity dependence of DPDI fluorescence in organic solvents, we considered that, while the interchromophoric interactions are weak in the nanoparticle, the excited singlet state migrates in a nanoparticle owing to energy hopping and is quenched at the surface, leading to the observed size-dependent fluorescence quantum yield (Φ_f) and a smaller value of Φ_f for nanoparticles than for the molecules in nonpolar solvents

Confining the state of light to a quantum manifold by engineered two-photon loss

Physical systems usually exhibit quantum behavior, such as superpositions and entanglement, only when they are sufficiently decoupled from a lossy environment. Paradoxically, a specially engineered interaction with the environment can become a resource for the generation and protection of quantum states. This notion can be generalized to the confinement of a system into a manifold of quantum states, consisting of all coherent superpositions of multiple stable steady states. We have experimentally confined the state of a harmonic oscillator to the quantum manifold spanned by two coherent states of opposite phases. In particular, we have observed a Schrodinger cat state spontaneously squeeze out of vacuum, before decaying into a classical mixture. This was accomplished by designing a superconducting microwave resonator whose coupling to a cold bath is dominated by photon pair exchange. This experiment opens new avenues in the fields of nonlinear quantum optics and quantum information, where systems with multi-dimensional steady state manifolds can be used as error corrected logical qubits

Non-Poissonian Quantum Jumps of a Fluxonium Qubit due to Quasiparticle Excitations

As the energy relaxation time of superconducting qubits steadily improves, non-equilibrium quasiparticle excitations above the superconducting gap emerge as an increasingly relevant limit for qubit coherence. We measure fluctuations in the number of quasiparticle excitations by continuously monitoring the spontaneous quantum jumps between the states of a fluxonium qubit, in conditions where relaxation is dominated by quasiparticle loss. Resolution on the scale of a single quasiparticle is obtained by performing quantum non-demolition projective measurements within a time interval much shorter than $T_1$, using a quantum limited amplifier (Josephson Parametric Converter). The quantum jumps statistics switches between the expected Poisson distribution and a non-Poissonian one, indicating large relative fluctuations in the quasiparticle population, on time scales varying from seconds to hours. This dynamics can be modified controllably by injecting quasiparticles or by seeding quasiparticle-trapping vortices by cooling down in magnetic field

Study of light-induced formation of photodimers in the i-motif nucleic acid structure by rapid-scan FTIR difference spectroscopy and hybrid hard- and soft-modelling

The i-motif is a DNA structure formed by cytosine-rich sequences, very relevant from a biochemical point of view and potentially useful in Nanotechnology as pH-sensitive nanodevices or nanomotors. To provide a different view on the structural changes and dynamics of direct excitation processes involving i-motif structures, the use of rapid scan FTIR spectroscopy is proposed. Hybrid hard- and soft-modelling based on the Multivariate Curve Resolution by Alternating least squares (MCR-ALS) algorithm has been used for the resolution of rapid-scan FTIR spectra and the interpretation of the photochemically induced time-dependent conformational changes of i-motif structures. The hybrid hard- and soft-modelling version of MCR-ALS (HS-MCR), which allows the introduction of kinetic models to describe the process behavior, provides also rate constants associated with the transitions modeled. The results show that i-motif structures formed by short DNA sequences present higher structural changes upon UV irradiation than those formed by long sequences with additional structural stabilizing elements, such as hairpins

Study of conformational transitions of i-motif DNA using time-resolved fluorescence and multivariate analysis methods

Recently, the presence of i-motif structures at C-rich sequences in human cells and their regulatory functions have been demonstrated. Despite numerous steady-state studies on i-motif at neutral and slightly acidic pH, the number and nature of conformation of this biological structure are still controversial. In this work, the fluorescence lifetime of labelled molecular beacon i-motif-forming DNA sequences at different pH values is studied. The influence of the nature of bases at the lateral loops and the presence of a Watson-Crick-stabilized hairpin are studied by means of time-correlated single-photon counting technique. This allows characterizing the existence of several conformers for which the fluorophore has lifetimes ranging from picosecond to nanosecond. The information on the existence of different i-motif structures at different pH values has been obtained by the combination of classical global decay fitting of fluorescence traces, which provides lifetimes associated with the events defined by the decay of each sequence and multivariate analysis, such as principal component analysis or multivariate curve resolution based on alternating least squares. Multivariate analysis, which is seldom used for this kind of data, was crucial to explore similarities and differences of behaviour amongst the different DNA sequences and to model the presence and identity of the conformations involved in the pH range of interest. The results point that, for i-motif, the intrachain contact formation and its dissociation show lifetimes ten times faster than for the open form of DNA sequences. They also highlight that the presence of more than one i-motif species for certain DNA sequences according to the length of the sequence and the composition of the bases in the lateral loop