The ability of extreme sound energy confinement with high-quality factor (Q-factor) resonance is of vital importance for acoustic devices requiring high intensity and hypersensitivity in biological ultrasonics, enhanced collimated sound emission (i.e
. sound laser) and high-resolution sensing. However, structures reported so far demonstrated a limited quality factor (Q-factor) of acoustic resonances, up to several tens in an open resonator. The emergence of bound states in the continuum (BIC) makes it possible to realize high-Q factor acoustic modes. Here, we report the theoretical design and experimental demonstration of acoustic BICs supported by a single open resonator. We predicted that such an open acoustic resonator could simultaneously support three types of BICs, including symmetry protected BIC, Friedrich-Wintgen BIC induced by mode interference, as well as a new kind of BIC: mirror-symmetry induced BIC. We also experimentally demonstrated the existence of all three types of BIC with Q-factor up to one order of magnitude greater than the highest Q-factor reported in an open resonator.
Two dimensional (2D) transition metal dichalcogenide (TMDC) materials, such as MoS2, WS2, MoSe2, and WSe2, have received extensive attention in the past decade due to their extraordinary physical properties. The unique properties make them become ide
al materials for various electronic, photonic and optoelectronic devices. However, their performance is limited by the relatively weak light-matter interactions due to their atomically thin form factor. Resonant nanophotonic structures provide a viable way to address this issue and enhance light-matter interactions in 2D TMDCs. Here, we provide an overview of this research area, showcasing relevant applications, including exotic light emission, absorption and scattering features. We start by overviewing the concept of excitons in 1L-TMDC and the fundamental theory of cavity-enhanced emission, followed by a discussion on the recent progress of enhanced light emission, strong coupling and valleytronics. The atomically thin nature of 1L-TMDC enables a broad range of ways to tune its electric and optical properties. Thus, we continue by reviewing advances in TMDC-based tunable photonic devices. Next, we survey the recent progress in enhanced light absorption over narrow and broad bandwidths using 1L or few-layer TMDCs, and their applications for photovoltaics and photodetectors. We also review recent efforts of engineering light scattering, e.g., inducing Fano resonances, wavefront engineering in 1L or few-layer TMDCs by either integrating resonant structures, such as plasmonic/Mie resonant metasurfaces, or directly patterning monolayer/few layers TMDCs. We then overview the intriguing physical properties of different types of van der Waals heterostructures, and their applications in optoelectronic and photonic devices. Finally, we draw our opinion on potential opportunities and challenges in this rapidly developing field of research.
We propose a universal strategy to realize a broadband control on arbitrary scatterers, through multiple coherent beams. By engineering the phases and amplitudes of incident beams, one can suppress the dominant scattering partial waves, making the ob
stacle lose its intrinsic responses in a broadband spectrum. The associated coherent beams generate a finite and static region, inside which the corresponding electric field intensity and Poynting vector vanish. As a solution to go beyond the sum-rule limit, our methodology is also irrespective of inherent system properties, as well as extrinsic operating wavelength, providing a non-invasive control on the wave-obstacles interaction for any kinds of shape.
Multimode interference and multipolar interplay govern functionalities of optical nanoresonators and nonlinear nanoantennas. Recently, excitation of the high-quality supercavity modes (quasi-BIC states) in individual subwavelength dielectric particle
s has been predicted to boost the nonlinear frequency conversion at the nanoscale. Here, we put forward the multipolar model which captures the physics behind linear and nonlinear response driven by such high-$Q$ modes in nanoresonators. We show that formation of the quasi-BIC state in the AlGaAs nanodisk can be understood through multipolar transformations of coupled leaky modes. In particular, the hybridized axially symmetric TE-polarized modes can be viewed as superpositions of multipoles, with a basis of parent multipoles constituted mainly by magnetic dipoles and octupole. The quasi-BIC point in the parameter space appears where dipolar losses are totally suppressed. The efficient optical coupling to this state is implemented via azimuthally polarized beam illumination matching its multipolar origin. We establish a one-to-one correspondence between the standard non Hermitian coupled-mode theory and multipolar models that enables transparent interpretation of scattering characteristics. Using our approach, we derive the multipolar composition of the generated second-harmonic radiation from the AlGaAs nanodisk and validate it with full-wave numerical simulations. Back-action of the second-harmonic radiation onto the fundamental frequency is taken into account in the coupled nonlinear model with pump depletion. A hybrid metal-dielectric nanoantenna is proposed to augment the conversion efficiency up to tens of per cent and actualize the nonlinear parametric downconversion. Our findings delineate the in-depth conceptual framework and novel promising strategies in the design of functional elements for nonlinear nanophotonics applications.
High index dielectric nanostructure supports different types of resonant modes. However, it is very challenging to achieve high-Q factor in a single subwavelength dielectric nanoresonator due to non-hermtian property of the open system. Here, we pres
ent a universal approach of finding out a series of high-Q resonant modes in a single nonspherical dielectric nanocavity by exploring quasi-bound state in the continuum. Unlike conventional method relying on heavy computation (ie, frequency scanning by FDTD), our approach is built upon leaky mode engineering, through which many high-Q modes can be easily achieved by constructing avoid-crossing (or crossing) of the eigenvalue for pair leaky modes. The Q-factor can be up to 2.3*10^4 for square subwavelength nanowire (NW) (n=4), which is 64 times larger than the highest Q-factor (Q=360) reported so far in single subwavelength nanodisk. Such high-Q modes can be attributed to suppressed radiation in the corresponding eigenchannels and simultaneously quenched electric(magnetic) at momentum space. As a proof of concept, we experimentally demonstrate the emergence of the high-Q resonant modes (Q=380) in the scattering spectrum of a single silicon subwavelength nanowire.
The microstructural features and high-temperature oxidation resistance of hybrid (TiC+TiB) networks reinforced Ti-6Al-4V composites were investigated after fabricated with reaction hot pressing technique. The inhomogeneous distribution of hybrid rein
forcers resulted in a sort of stress-induced grain refinement for {alpha}-Ti matrix phase, which was further facilitated by heterogeneous nucleation upon additive interfaces. HRTEM analyses revealed the crystallographic orientation relation between TiB and alpha-Ti phases as (201)TiB//(-1100)alpha-Ti plus [11-2]//[0001] alpha-Ti, while TiC and {alpha}-Ti phases maintained the interrelation of (-200)TiC//(-2110) {alpha}-Ti and [001]TiC//[01-10] alpha-Ti. The hybridly reinforced Ti-6Al-4V/(TiC+TiB) composites displayed superior oxidation resistance to both the sintered matrix alloy and the two composites reinforced solely with TiC or TiB addition during the cyclic oxidation at 873, 973 and 1073 K respectively for 100 h. The hybrid reinforcers volume fraction was a more influential factor to improve oxidation resistance than the matrix alloy powder size. As temperature rose from 873 to 1073 K, the oxidation kinetics transferred from the nearly parabolic type through qusilinear tendency into the finally linear mode. This corresponded to the morphological transition of oxide scales from a continuous protective film to a partially damaged layer and ended up with the complete spallation of alternating alumina and rutile multilayers. A phenomenological model was proposed to elucidate the growth process of oxides scales. The release of thermal stress, the suppression of oxygen diffusion and the fastening of oxide adherence were found as the three major mechanisms to enhance the oxidation resistance of hybrid reinforced composites.
It has been widely accepted that the introduction of titanium carbides into titanium-based alloys can significantly enhance the oxidation resistance due to their superior physicochemical stability at elevated temperatures. The present study reported
for the first time that the ordered C vacancies within titanium carbides could lead to an uncommon phenomenon particularly at the very initial stage of oxidation. The intrinsic micro-to-macro oxidation mechanisms were systematically clarified with the aids of transmission electron microscope and ab-initio molecular dynamics simulation.
We report that the refractive index of transition metal dichacolgenide (TMDC) monolayers, such as MoS2, WS2, and WSe2, can be substantially tuned by > 60% in the imaginary part and > 20% in the real part around exciton resonances using CMOS-compatibl
e electrical gating. This giant tunablility is rooted in the dominance of excitonic effects in the refractive index of the monolayers and the strong susceptibility of the excitons to the influence of injected charge carriers. The tunability mainly results from the effects of injected charge carriers to broaden the spectral width of excitonic interband transitions and to facilitate the interconversion of neutral and charged excitons. The other effects of the injected charge carriers, such as renormalizing bandgap and changing exciton binding energy, only play negligible roles. We also demonstrate that the atomically thin monolayers, when combined with photonic structures, can enable the efficiencies of optical absorption (reflection) tuned from 40% (60%) to 80% (20%) due to the giant tunability of refractive index. This work may pave the way towards the development of field-effect photonics in which the optical functionality can be controlled with CMOS circuits.
Transition metal dichalcogenide (TMDC) monolayers present a remarkable multifunctional material with potential to enable the development of a wide range of novel devices. However, the functionalities observed often fall short of the expectation, whic
h hinders the device development. Here we demonstrate that the optical, catalytic, and thermal functionalities of TMDC monolayers can all be substantially enhanced by up to orders of magnitude with the intercalation of water molecules or small cations (H+ and Li+) between the monolayers and underlying substrates. In contrast, the same molecules or cations adsorbed on top of the monolayers show negligible effects. We also discover two major roles of the intercalated species in the enhancement: doping the monolayers and modifying the interaction of the monolayers with the substrate. The result points out a versatile and convenient strategy of using the intercalation of molecules or ions to enhance the functionalities of TMDC monolayers.
Enabling perfect light absorption in ultrathin materials promises the development of exotic photonic devices. Here we demonstrate new strategies that can provide capabilities to rationally design ultrathin (thickness < {lambda}/10~{lambda}/5) semicon
ductor perfect absorbers for arbitrary wavelengths, including those at which the intrinsic absorption of the semiconductor is weak, e.g. Si for near-IR wavelengths. This is in stark contrast with the existing studies on ultrathin perfect absorbers, which have focused on metallic materials or highly-absorptive semiconductors. Our design strategies are built upon an intuitive model, coupled leaky mode theory that we recently developed and can turn the design for perfect absorbers to the design for leaky modes. The designed absorber is featured with extraordinary absorption enhancement, miniaturized dimension, and high selectivity for the wavelength, polarization, and angle of incident light. It can enable the development of flexible, light-weight, high-performance, cost-effective, and multifunctional optoelectronic devices that are difficult with current light absorbers.
