The random field Ising model is studied numerically at both zero and positive temperature. Ground states are mapped out in a region of random field and external field strength. Thermal states and thermodynamic properties are obtained for all temperatures using the Wang-Landau algorithm. The specific heat and susceptibility typically display sharp peaks in the critical region for large systems and strong disorder. These sharp peaks result from large domains flipping. For a given realization of disorder, ground states and thermal states near the critical line are found to be strongly correlated--a concrete manifestation of the zero temperature fixed point scenario.
In this paper the three-dimensional random-field Ising model is studied at both zero temperature and positive temperature. Critical exponents are extracted at zero temperature by finite size scaling analysis of large discontinuities in the bond energy. The heat capacity exponent ␣ is found to be near zero. The ground states are determined for a range of external field and disorder strength near the zero temperature critical point and the scaling of ground state tilings of the field-disorder plane is discussed. At positive temperature the specific heat and the susceptibility are obtained using the Wang-Landau algorithm. It is found that sharp peaks are present in these physical quantities for some realizations of systems sized 16 3 and larger. These sharp peaks result from flipping large domains and correspond to large discontinuities in ground state bond energies. Finally, zero temperature and positive temperature spin configurations near the critical line are found to be highly correlated suggesting a strong version of the zero temperature fixed point hypothesis.
Several configurations of multi-beam reconfigurable THz antennas based on graphene have been investigated. Two modulation mechanisms of graphene-based THz antenna are introduced, one is the reflector-transmission window model, and the other is the reflector-director model (Yagi-Uda antenna). The main parameters, such as main beam direction, resonance frequency, peak gain, and the front-to-back ratio of the proposed antenna can be controlled by adjusting the chemical potentials of the graphene in the antenna. Moreover, this paper provides an easy way to obtain complex graphene-based multi-beam antennas, showing strong potential in the design of other complex graphene-based systems, enabling nanoscale wireless communications and sensing devices for different applications. INDEX TERMS Graphene, multi-beam, reconfigurable, THz antenna.
Transcranial low-intensity ultrasound is a promising neuromodulation modality, with the advantages of noninvasiveness, deep penetration, and high spatiotemporal accuracy. However, the underlying biological mechanism of ultrasonic neuromodulation remains unclear, hindering the development of efficacious treatments. Here, the well-known Piezo1 was studied through a conditional knockout mouse model as a major mediator for ultrasound neuromodulation ex vivo and in vivo. We showed that Piezo1 knockout (P1KO) in the right motor cortex of mice significantly reduced ultrasound-induced neuronal calcium responses, limb movement, and muscle electromyogram (EMG) responses. We also detected higher Piezo1 expression in the central amygdala (CEA), which was found to be more sensitive to ultrasound stimulation than the cortex was. Knocking out the Piezo1 in CEA neurons showed a significant reduction of response under ultrasound stimulation, while knocking out astrocytic Piezo1 showed no-obvious changes in neuronal responses. Additionally, we excluded an auditory confound by monitoring auditory cortical activation and using smooth waveform ultrasound with randomized parameters to stimulate P1KO ipsilateral and contralateral regions of the same brain and recording evoked movement in the corresponding limb. Thus, we demonstrate that Piezo1 is functionally expressed in different brain regions and that it is an important mediator of ultrasound neuromodulation in the brain, laying the ground for further mechanistic studies of ultrasound.
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