Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userOptically tunable microresonator using an azobenzene monolayer
58
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
Photoswitchable organic molecules can undergo reversible structural changes with an external light stimulus. These optically controlled molecules have been used in the development of smart polymers, optical writing of grating films, and even controllable in-vivo drug release. Being the simplest class of photoswitches in terms of structure, azobenzenes have become the most ubiquitous, well-characterized, and implemented organic molecular switch. Given their predictable response, they are ideally suited to create an all-optically controlled switch. However, fabricating a monolithic optical device comprised solely from azobenzene while maintaining the photoswitching functionality is challenging. In this work, we combine integrated photonics with optically switchable organic molecules to create an optically controlled integrated device. A silica toroidal resonant cavity is functionalized with a monolayer of an azobenzene derivative. After functionalization, the loaded cavity Q is above 100,000. When 450 nm light is coupled into cavity resonance, the azobenzene isomerizes from trans-isomer to cis-isomer, inducing a refractive index change. Because the resonant wavelength of the cavity is governed by the index, the resonant wavelength changes in parallel. At the probe wavelength of 1300 nm, the wavelength shift is determined by the duration and intensity of the 450 nm light and the density of azobenzene functional groups on the device surface, providing multiple control mechanisms. Using this photoswitchable device, resonance frequency tuning as far as sixty percent of the cavity free spectral range in the near-IR is demonstrated. The kinetics of the tuning are in agreement with spectroscopic and ellipsometry measurements coupled with finite element method calculations.
rate research
Read More
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.
We present a monolayer black phosphorus (BP)-based metamaterial structure for tunable anisotropic absorption in the mid-infrared. Based on the critical coupling mechanism of guided resonance, the structure realizes the high absorption efficiency of 99.65$%$ for TM polarization, while only 2.61$%$ at the same wavelength for TE polarization due to the intrinsic anisotropy of BP. The absorption characteristics can be flexibly controlled by changing critical coupling conditions, including the electron doping of BP, geometric parameters and incident angles of light. The results show feasibility in designing high-performance BP-based optoelectronic devices with spectral tunability and polarization selectivity.
We report on the first experimental demonstration of widely-tunable parametric sideband generation in a Kerr microresonator. Specifically, by pumping a silica microsphere in the normal dispersion regime, we achieve the generation of phase-matched four-wave mixing sidebands at large frequency detunings from the pump. Thanks to the role of higher-order dispersion in enabling phase matching, small variations of the pump wavelength translate into very large and controllable changes in the wavelengths of the generated sidebands: we experimentally demonstrate over 720 nm of tunability using a low-power continuous-wave pump laser in the C-band. We also derive simple theoretical predictions for the phase-matched sideband frequencies, and discuss the predictions in light of the discrete cavity resonance frequencies. Our experimentally measured sideband wavelengths are in very good agreement with theoretical predictions obtained from our simple phase matching analysis.
Strong light-matter interactions within nanoscale structures offer the possibility of optically controlling material properties. Motivated by the recent discovery of intrinsic long-range magnetic order in two-dimensional materials, which allows for the creation of novel magnetic devices of unprecedented small size, we predict that light can couple with magnetism and efficiently tune magnetic orders of monolayer ruthenium trichloride (RuCl3). First-principles calculations show that both free carriers and optically excited electron-hole pairs can switch monolayer RuCl3 from the proximate spin-liquid phase to a stable ferromagnetic phase. Specifically, a moderate electron-hole pair density (on the order of 10^13 cm-2) can significantly stabilize the ferromagnetic phase by 10 meV/f.u. in comparison to the zigzag phase, so that the predicted ferromagnetism can be driven by optical pumping experiments. Analysis shows that this magnetic phase transition is driven by a combined effect of doping-induced lattice strain and itinerant ferromagnetism. According to the Ising-model calculation, we find that the Curie temperature of the ferromagnetic phase can be increased significantly by raising carrier or electron-hole pair density. This enhanced opto-magnetic effect opens new opportunities to manipulate two-dimensional magnetism through non-contact, optical approaches.
We theoretically investigate the terahertz dielectric response of a semiconductor slab hosting an infrared photoinduced grating. The periodic structure is due to the charge carries photo-excited by the interference of two tilted infrared plane waves so that the grating depth and period can be tuned by modifying the beam intensities and incidence angles, respectively. In the case where the grating period is much smaller than the terahertz wavelength, we numerically evaluate the ordinary and extraordinary component of the effective permittivity tensor by resorting to electromagnetic full-wave simulation coupled to the dynamics of charge carries excited by infrared radiation. We show that the photoinduced metamaterial optical response can be tailored by varying the grating and it ranges from birefringent to hyperbolic to anisotropic negative dielectric without resorting to microfabrication.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
