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Register a new userLight Programmable Micro/Nanomotors with Optically Tunable In-Phase Electric Polarization
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To develop active nanomaterials that can instantly respond to external stimuli with designed mechanical motions is an important step towards the realization of nanomachines and nanorobots. Herein, we present our finding of a versatile working mechanism that allows instantaneous change of alignment direction and speed of semiconductor nanowires in an external electric field with simple visible-light exposure. The light induced alignment switch can be cycled over hundreds of times and programmed to express words in Morse code. With theoretical analysis and numerical simulation, the working principle can be attributed to the optically tuned real-part (in-phase) electrical polarization of a semiconductor nanowire in an aqueous suspension. The manipulation principle is exploited to create a new type of microscale stepper motor that can readily switch between in-phase and out-phase modes, and agilely operate independent of neighboring motors with patterned light. This work could inspire the development of a new type of micro/nanomachines with individual and reconfigurable maneuverability for many applications.
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Highly efficient and widely applicable working mechanisms that allow nanomaterials and devices to respond to external stimuli with controlled mechanical motions could make far-reaching impact to reconfigurable, adaptive, and robotic nanodevices. Here, we report an innovative mechanism that allows multifold reconfiguration of mechanical rotation of semiconductor nanoentities in electric (E) fields by visible light stimulation. When illuminated by light in the visible to infrared range, the rotation speed of semiconductor Si nanowires in electric fields can instantly increase, decrease, and even reverse the orientation depending on the intensity of the applied light and the AC E-field frequency. This multifold rotation configuration is highly efficient, instant, and facile. Switching between different modes can be simply controlled by the light intensity at an AC frequency. An array of experimentations, theoretical analysis, and simulations are carried out to understand the underlying principle, which can be attributed to the optically tunable polarization of Si nanowires in aqueous suspension and an external electric field. Finally, leveraging this newly discovered effect, we successfully differentiate semiconductor and metallic nanoentities in a non-contact and non-destructive manner. This research could inspire a new class of reconfigurable nanoelectromechanical and nanorobotic devices for optical sensing, communication, molecule release, detection, nanoparticle separation, and microfluidic automation.
Mechanical systems are one of the promising platforms for classical and quantum information processing and are already widely-used in electronics and photonics. Cavity optomechanics offers many new possibilities for information processing using mechanical degrees of freedom; one of them is storing optical signals in long-lived mechanical vibrations by means of optomechanically induced transparency. However, the memory storage time is limited by intrinsic mechanical dissipation. More over, in-situ control and manipulation of the stored signals--processing--has not been demonstrated. Here, we address both of these limitations using a multi-mode cavity optomechanical memory. An additional optical field coupled to the memory modifies its dynamics through time-varying parametric feedback. We demonstrate that this can extend the memory decay time by an order of magnitude, decrease its effective mechanical dissipation rate by two orders of magnitude, and deterministically shift the phase of a stored field by over 2$pi$. This further expands the information processing toolkit provided by cavity optomechanics.
A theoretical variation between the two distinct light-matter coupling regimes, namely weak and strong coupling, becomes uniquely feasible in open optical Fabry-Perot microcavities with low mode volume, as discussed here. In combination with monolayers of transition-metal dichalcogenides (TMDCs) such as WS2, which exhibits a large exciton oscillator strength and binding energy, the room-temperature observation of hybrid bosonic quasiparticles, referred to as exciton-polaritons and characterized by a Rabi splitting, comes into reach. In this context, our simulations using the transfer-matrix method show how to tailor and alter the coupling strength actively by varying the relative field strength at the excitons position - exploiting a tunable cavity length, a transparent PMMA spacer layer and angle-dependencies of optical resonances. Continuously tunable coupling for future experiments is hereby proposed, capable of real-time adjustable Rabi splitting as well as switching between the two coupling regimes. Being nearly independent of the chosen material, the suggested structure could also be used in the context of light-matter-coupling experiments with quantum dots, molecules or quantum wells. While the adjustable polariton energy levels could be utilized for polariton-chemistry or optical sensing, cavities that allow working at the exceptional point promise the exploration of topological properties of that point.
The tantalizing promise of quantum computational speedup in solving certain problems has been strongly supported by recent experimental evidence from a high-fidelity 53-qubit superconducting processor1 and Gaussian boson sampling (GBS) with up to 76 detected photons. Analogous to the increasingly sophisticated Bell tests that continued to refute local hidden variable theories, quantum computational advantage tests are expected to provide increasingly compelling experimental evidence against the Extended Church-Turing thesis. In this direction, continued competition between upgraded quantum hardware and improved classical simulations is required. Here, we report a new GBS experiment that produces up to 113 detection events out of a 144-mode photonic circuit. We develop a new high-brightness and scalable quantum light source, exploring the idea of stimulated squeezed photons, which has simultaneously near-unity purity and efficiency. This GBS is programmable by tuning the phase of the input squeezed states. We demonstrate a new method to efficiently validate the samples by inferring from computationally friendly subsystems, which rules out hypotheses including distinguishable photons and thermal states. We show that our noisy GBS experiment passes the nonclassicality test using an inequality, and we reveal non-trivial genuine high-order correlation in the GBS samples, which are evidence of robustness against possible classical simulation schemes. The photonic quantum computer, Jiuzhang 2.0, yields a Hilbert space dimension up to $10^{43}$, and a sampling rate $10^{24}$ faster than using brute-force simulation on supercomputers.
In this paper, a broadband tunable polarization converter based on graphene metasurfaces is proposed. This polarization converter works in the terahertz (THz) frequency region, using the advantage of graphene characteristics to have a tunable frequency response. The designed graphene-shaped periodic structure on top of the substrate is utilized to convert the incident wave polarization to the desired target in a flexible operational band in the THz frequencies. The polarization conversion ratio is more than 0.85 in a wide range of frequencies in the THz band from 4.86 to 8.42 THz (the fractional bandwidth is 54%). The proposed polarization converter is insensitive to the angle of the incident wave up to 40{deg}. Using graphene provides a tunable frequency response without changing the geometry of the designed structure.
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