Quantum-limited amplification and parametric instability in the reversed dissipation regime of cavity optomechanics

Cavity optomechanical phenomena, such as cooling, amplification or optomechanically induced transparency, emerge due to a strong imbalance in the dissipation rates of the parametrically coupled electromagnetic and mechanical resonators. Here we analyze the reversed dissipation regime where the mechanical energy relaxation rate exceeds the energy decay rate of the electromagnetic cavity. We demonstrate that this regime allows for mechanically-induced amplification (or cooling) of the electromagnetic mode. Gain, bandwidth, and added noise of this electromagnetic amplifier are derived and compared to amplification in the normal dissipation regime. In addition, we analyze the parametric instability, i.e. optomechanical Brillouin lasing, and contrast it to conventional optomechanical phonon lasing. Finally, we propose an experimental scheme that realizes the reversed dissipation regime using parametric coupling and optomechanical cooling with a second electromagnetic mode enabling quantum-limited amplification. Recent advances in high-Q superconducting microwave resonators make the reversed dissipation regime experimentally realizable.Comment: 5+3 pages, 5 figures, 1 tabl

Quantum-limited amplification and parametric instability in the reversed dissipation regime of cavity optomechanics.

Cavity optomechanical phenomena, such as cooling, amplification, or optomechanically induced transparency, emerge due to a strong imbalance in the dissipation rates of the parametrically coupled electromagnetic and mechanical resonators. Here we analyze the reversed dissipation regime where the mechanical energy relaxation rate exceeds the energy decay rate of the electromagnetic cavity. We demonstrate that this regime allows for mechanically induced amplification (or cooling) of the electromagnetic mode. Gain, bandwidth, and added noise of this electromagnetic amplifier are derived and compared to amplification in the normal dissipation regime. In addition, we analyze the parametric instability, i.e., optomechanical Brillouin lasing, and contrast it to conventional optomechanical phonon lasing. Finally, we propose an experimental scheme that realizes the reversed dissipation regime using parametric coupling and optomechanical cooling with a second electromagnetic mode enabling quantum-limited amplification. Recent advances in high-Q superconducting microwave resonators make the reversed dissipation regime experimentally realizable

Rare earth spin ensemble magnetically coupled to a superconducting resonator

Interfacing superconducting quantum processors, working in the GHz frequency range, with optical quantum networks and atomic qubits is a challenging task for the implementation of distributed quantum information processing as well as for quantum communication. Using spin ensembles of rare earth ions provide an excellent opportunity to bridge microwave and optical domains at the quantum level. In this letter, we demonstrate magnetic coupling of Er$^{3+}$ spins doped in Y$_{2}$SiO$_{5}$ crystal to a high-Q coplanar superconducting resonator.Comment: 5 pages, 3 figure

Electron microscopy analysis of ATP-independent nucleosome unfolding by FACT

FACT is a histone chaperone that participates in nucleosome removal and reassembly during transcription and replication. We used electron microscopy to study FACT, FACT:Nhp6 and FACT:Nhp6:nucleosome complexes, and found that all complexes adopt broad ranges of configurations, indicating high flexibility. We found unexpectedly that the DNA binding protein Nhp6 also binds to the C-terminal tails of FACT subunits, inducing more open geometries of FACT even in the absence of nucleosomes. Nhp6 therefore supports nucleosome unfolding by altering both the structure of FACT and the properties of nucleosomes. Complexes formed with FACT, Nhp6, and nucleosomes also produced a broad range of structures, revealing a large number of potential intermediates along a proposed unfolding pathway. The data suggest that Nhp6 has multiple roles before and during nucleosome unfolding by FACT, and that the process proceeds through a series of energetically similar intermediate structures, ultimately leading to an extensively unfolded form

Acenaphthenoannulation Induced by the Dual Lewis Acidity of Alumina

We have discovered a dual (i. e., soft and hard) Lewis acidity of alumina that enables rapid one-pot π-extension through the activation of terminal alkynes followed by C−F activation. The tandem reaction introduces an acenaphthene fragment – an essential moiety of geodesic polyarenes. This reaction provides quick access to elusive non-alternant polyarenes such as π-extended buckybowls and helicenes through three-point annulation of the 1-(2-ethynyl-6-fluorophenyl)naphthalene moiety. The versatility of the developed method was demonstrated by the synthesis of unprecedented structural fragments of elusive geodesic graphene nanoribbons

The Complexation of Silver (I) ion with 18-Crown-6 Ether in Water and Some Polar Aprotic Solvents

Методом прямого потенциометрического титрования изучен процесс комплексообразования ионов серебра (I) с 18-краун-6 эфиром в среде некоторых полярных водно-апротонных растворителей при постоянной температуре 308 К. Константы устойчивости образующегося комплекса определены при различных мольных долях диметилсульфоксида и диметилформамида от 0,2 до 0,8 в составе смешанного растворителя. Показано, что, несмотря на одинаковую природу сорастворителей, они оказывают прямо противоположное действие на константу устойчивости комплекса вследствие неустойчивости ДМФА в кислой среде и при нагревании. Отмечено, что исследуемая реакция комплексообразования является экзотермичной, а повышение температуры уменьшает устойчивость исследуемых комплексовThe process of complexation of silver (I) ions with 18-crown-6 ether in some polar water-aproton solvents at a constant temperature of 308К was studied by direct potentiometric titration. The stability constants of the resulting complex are determined depending on the molar fraction from 0.2 to 0.8 dimethylsulfoxide and dimethylformamide in the composition of the mixed solvent. It is shown that, despite the same nature of the co-solvents, they have the opposite effect on the stability constant of the complex due to the instability of DMF in an acidic medium and when heated. It is noted that the studied reaction is exothermic and the temperature increase reduces the stability of the studied complexe

Josephson Coupling and Fiske Dynamics in Ferromagnetic Tunnel Junctions

We report on the fabrication of Nb/AlO_x/Pd_{0.82}Ni_{0.18}/Nb superconductor/insulator/ferromagnetic metal/superconductor (SIFS) Josephson junctions with high critical current densities, large normal resistance times area products, high quality factors, and very good spatial uniformity. For these junctions a transition from 0- to \pi-coupling is observed for a thickness d_F ~ 6 nm of the ferromagnetic Pd_{0.82}Ni_{0.18} interlayer. The magnetic field dependence of the \pi-coupled junctions demonstrates good spatial homogeneity of the tunneling barrier and ferromagnetic interlayer. Magnetic characterization shows that the Pd_{0.82}Ni_{0.18} has an out-of-plane anisotropy and large saturation magnetization, indicating negligible dead layers at the interfaces. A careful analysis of Fiske modes provides information on the junction quality factor and the relevant damping mechanisms up to about 400 GHz. Whereas losses due to quasiparticle tunneling dominate at low frequencies, the damping is dominated by the finite surface resistance of the junction electrodes at high frequencies. High quality factors of up to 30 around 200 GHz have been achieved. Our analysis shows that the fabricated junctions are promising for applications in superconducting quantum circuits or quantum tunneling experiments.Comment: 15 pages, 9 figure

Snake Cytotoxins Bind to Membranes via Interactions with Phosphatidylserine Head Groups of Lipids

The major representatives of Elapidae snake venom, cytotoxins (CTs), share similar three-fingered fold and exert diverse range of biological activities against various cell types. CT-induced cell death starts from the membrane recognition process, whose molecular details remain unclear. It is known, however, that the presence of anionic lipids in cell membranes is one of the important factors determining CT-membrane binding. In this work, we therefore investigated specific interactions between one of the most abundant of such lipids, phosphatidylserine (PS), and CT 4 of Naja kaouthia using a combined, experimental and modeling, approach. It was shown that incorporation of PS into zwitterionic liposomes greatly increased the membrane-damaging activity of CT 4 measured by the release of the liposome-entrapped calcein fluorescent dye. The CT-induced leakage rate depends on the PS concentration with a maximum at approximately 20% PS. Interestingly, the effects observed for PS were much more pronounced than those measured for another anionic lipid, sulfatide. To delineate the potential PS binding sites on CT 4 and estimate their relative affinities, a series of computer simulations was performed for the systems containing the head group of PS and different spatial models of CT 4 in aqueous solution and in an implicit membrane. This was done using an original hybrid computational protocol implementing docking, Monte Carlo and molecular dynamics simulations. As a result, at least three putative PS-binding sites with different affinities to PS molecule were delineated. Being located in different parts of the CT molecule, these anion-binding sites can potentially facilitate and modulate the multi-step process of the toxin insertion into lipid bilayers. This feature together with the diverse binding affinities of the sites to a wide variety of anionic targets on the membrane surface appears to be functionally meaningful and may adjust CT action against different types of cells