RESUMEN
The accumulation and extrusion of Ca2+ in the pre- and postsynaptic compartments play a critical role in initiating plastic changes in biological synapses. To emulate this fundamental process in electronic devices, we developed diffusive Ag-in-oxide memristors with a temporal response during and after stimulation similar to that of the synaptic Ca2+ dynamics. In situ high-resolution transmission electron microscopy and nanoparticle dynamics simulations both demonstrate that Ag atoms disperse under electrical bias and regroup spontaneously under zero bias because of interfacial energy minimization, closely resembling synaptic influx and extrusion of Ca2+, respectively. The diffusive memristor and its dynamics enable a direct emulation of both short- and long-term plasticity of biological synapses, representing an advance in hardware implementation of neuromorphic functionalities.
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A method is derived to solve the massless Dirac-Weyl equation describing electron transport in a monolayer of graphene with a scalar potential barrier U(x,t), homogeneous in the y direction, of arbitrary space and time dependence. Resonant enhancement of both electron backscattering and currents, across and along the barrier, is predicted when the modulation frequencies satisfy certain resonance conditions. These conditions resemble those for Shapiro steps of driven Josephson junctions. Surprisingly, we find a nonzero y component of the current for carriers of zero momentum along the y-axis.
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A Brownian particle moving across a porous membrane subject to an oscillating force exhibits stochastic resonance with properties which strongly depend on the geometry of the confining cavities on the two sides of the membrane. Such a manifestation of stochastic resonance requires neither energetic nor entropic barriers, and can thus be regarded as a purely geometric effect. The magnitude of this effect is sensitive to the geometry of both the cavities and the pores, thus leading to distinctive optimal synchronization conditions.
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Respiration in bacteria involves a sequence of energetically coupled electron and proton transfers creating an electrochemical gradient of protons (a proton-motive force) across the inner bacterial membrane. With a simple kinetic model, we analyze a redox loop mechanism of proton-motive force generation mediated by a molecular shuttle diffusing inside the membrane. This model, which includes six electron-binding and two proton-binding sites, reflects the main features of nitrate respiration in E. coli bacteria. We describe the time evolution of the proton translocation process. We find that the electron-proton electrostatic coupling on the shuttle plays a significant role in the process of energy conversion between electron and proton components. We determine the conditions where the redox loop mechanism is able to translocate protons against the transmembrane voltage gradient above 200 mV with a thermodynamic efficiency of about 37%, in the physiologically important range of temperatures from 250 to 350 K.
Asunto(s)
Membrana Celular/metabolismo , Difusión , Escherichia coli/citología , Escherichia coli/metabolismo , Modelos Biológicos , Fuerza Protón-Motriz , Protones , Transporte Biológico , Conductividad Eléctrica , Transporte de Electrón , Escherichia coli/enzimología , Hemo/metabolismo , Cinética , Temperatura , Vitamina K 2/metabolismoRESUMEN
A popular interpretation of the "collapse" of the wave function is as being the result of a local interaction ("measurement") of the quantum system with a macroscopic system ("detector"), with the ensuing loss of phase coherence between macroscopically distinct components of its quantum state vector. Nevetheless as early as in 1953 Renninger suggested a Gedankenexperiment, in which the collapse is triggered by non-observation of one of two mutually exclusive outcomes of the measurement, i.e., in the absence of interaction of the quantum system with the detector. This provided a powerful argument in favour of "physical reality" of (nonlocal) quantum state vector. In this paper we consider a possible version of Renninger's experiment using the light propagation through a birefringent quantum metamaterial. Its realization would provide a clear visualization of a wave function collapse produced by a "non-measurement", and make the concept of a physically real quantum state vector more acceptable.
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The intrinsic variability of switching behavior in memristors has been a major obstacle to their adoption as the next generation of universal memory. On the other hand, this natural stochasticity can be valuable for hardware security applications. Here we propose and demonstrate a novel true random number generator utilizing the stochastic delay time of threshold switching in a Ag:SiO2 diffusive memristor, which exhibits evident advantages in scalability, circuit complexity, and power consumption. The random bits generated by the diffusive memristor true random number generator pass all 15 NIST randomness tests without any post-processing, a first for memristive-switching true random number generators. Based on nanoparticle dynamic simulation and analytical estimates, we attribute the stochasticity in delay time to the probabilistic process by which Ag particles detach from a Ag reservoir. This work paves the way for memristors in hardware security applications for the era of the Internet of Things.Memristors can switch between high and low electrical-resistance states, but the switching behaviour can be unpredictable. Here, the authors harness this unpredictability to develop a memristor-based true random number generator that uses the stochastic delay time of threshold switching.
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A novel Ag/oxide-based threshold switching device with attractive features including ≈1010 nonlinearity is developed. High-resolution transmission electron microscopic analysis of the nanoscale crosspoint device suggests that elongation of an Ag nanoparticle under voltage bias followed by spontaneous reformation of a more spherical shape after power off is responsible for the observed threshold switching.
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Tantalum oxide memristors can switch continuously from a low-conductance semiconducting to a high-conductance metallic state. At the boundary between these two regimes are quantized conductance states, which indicate the formation of a point contact within the oxide characterized by multistable conductance fluctuations and enlarged electronic noise. Here, we observe diverse conductance-dependent noise spectra, including a transition from 1/f(2) (activated transport) to 1/f (flicker noise) as a function of the frequency f, and a large peak in the noise amplitude at the conductance quantum GQ=2e(2)/h, in contrast to suppressed noise at the conductance quantum observed in other systems. We model the stochastic behaviour near the point contact regime using Molecular Dynamics-Langevin simulations and understand the observed frequency-dependent noise behaviour in terms of thermally activated atomic-scale fluctuations that make and break a quantum conductance channel. These results provide insights into switching mechanisms and guidance to device operating ranges for different applications.
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We numerically simulated the diffusion of a charged Brownian particle confined to a plane under the action of an orthogonal magnetic field with intensity depending on the distance from a center. Despite its apparent simplicity, this system exhibits anomalous diffusion. For positive field gradients, radial and angular dynamics are asymptotically subdiffusive, with exponents given by simple analytical expressions. In contrast, when driven by a weakly decaying field, the particle attains normal diffusion only after exceedingly long superdiffusive transients. These mechanisms can be related to Bohm diffusion in magnetized plasmas.
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We consider the unidirectional particle transport in a suspension of colloidal particles which interact with each other via a pair potential having a hard-core repulsion plus an attractive tail. The colloids are confined within a long narrow channel and are driven along by a dc or an ac external potential. In addition, the walls of the channel interact with the particles via a ratchetlike periodic potential. We use dynamical density functional theory to compute the average particle current. In the case of dc drive, we show that as the attraction strength between the colloids is increased beyond a critical value, the stationary density distribution of the particles loses its stability leading to depinning and a time-dependent density profile. Attraction induced symmetry breaking gives rise to the coexistence of stable stationary density profiles with different spatial periods and time-periodic density profiles, each characterized by different values for the particle current.
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Geometric stochastic resonance of particles diffusing across a porous membrane subject to oscillating forces is characterized as a synchronization process. Noninteracting particle currents through a symmetric membrane pore are driven either perpendicular or parallel to the membrane, whereas, harmonic-mixing spectral current components are generated by the combined action of perpendicular and parallel drives. In view of potential applications to the transport of colloids and biological molecules through narrow pores, we also consider the role of particle repulsion as a controlling factor.
Asunto(s)
Biofisica/métodos , Coloides/química , Membranas/química , Algoritmos , Transporte Biológico , Simulación por Computador , Difusión , Modelos Estadísticos , Oscilometría/métodos , Porosidad , Procesos EstocásticosRESUMEN
We consider an elastic neutral dimer formed by two bound equal masses carrying opposite charges and moving along an electrically active filament in one dimension. An ac electrical field drives the two dimer heads, when set free or bound together to form a rigid rod, to opposite directions, thus yielding a zero net dimer current for zero and infinite elastic constants. Under the same driving conditions, an elastically deformable dimer can get rectified and the ensuing net current maximized for an optimal value of dimer elastic constant. The dependence of the dimer current on the periodic charge distribution along the filament is analyzed in terms of global symmetries of the dimer dynamics.