Abstract:Natural hyperbolic materials with dielectric permittivities of opposite sign along different principal axes can confine long-wavelength electromagnetic waves down to the nanoscale, well below the diffraction limit. This has been demonstrated using hyperbolic phonon polaritons (HPP) in hexagonal boron nitride (hBN) and -MoO 3 , among other materials. However, HPP dissipation at ambient conditions is substantial and its fundamental limits remain unexplored 1,2 . Here, we exploit cryogenic nano-infrared imaging … Show more
“…This is clear evidence of geometric confinement, considering that, in RB3, numerically calculated Q factors from freestanding area (Figure a, red line) are slightly smaller than those from the supported area (Figure a, black line). The large Q factors of up to 40 in spatially confined freestanding α-MoO 3 is 2–4 times higher than previously reported values ,,, (see Table S1) in α-MoO 3 , even surpassing those obtained at the temperature as low as 50 K, where the temperature-dependent PhP damping is largely suppressed. Compared to the reduced temperature, submicron freestanding channels of hyperbolic materials presented in this work can be more conveniently realized and thus promising for real applications.…”
Section: Resultscontrasting
confidence: 58%
“…Within the x – y plane, hyperbolic PhPs propagate along the [001] and [100] directions in RB1 and RB2, respectively, and elliptic PhPs propagate in the x – y plane in RB3, resulting in anisotropic PhPs . The remarkably low loss of PhPs in α-MoO 3 , compared to counterparts such as boron nitride and graphene , can potentially lead to practical applications in IR signal processing and heat transfer . Due to strong crystallinity of each layer of α-MoO 3 , twistronics can also be readily experienced in this material. − Twisted double layer α-MoO 3 has been shown to be able to manipulate light at the nanoscale with topological transitions that bring huge potential to nanophotonics and polaritonics. − In addition to twisting the angle between adjacent α-MoO 3 layers, PhPs can also be engineered by other approaches, including patterning their microstructures, , changing the material composition, , and controlling the surrounding dielectric environment. , …”
Highly confined and in-plane anisotropic
phonon-polaritons (PhPs)
in orthorhombic-phase molybdenum trioxide (α-MoO3) exist in three Reststrahlen bands (RB) in the mid-infrared regime
where the crystal exhibits negative permittivity along three principal
axes. However, PhP behaviors in geometrically confined α-MoO3 remain enigmatic. Here, we investigated PhPs confined in
freestanding α-MoO3 covering submicron-width trenches.
We remarkably observed opposite trends in terms of PhP wavelengths
in two RBs for PhPs propagating on supported and spatially confined
freestanding α-MoO3. Due to the geometric confinement
in the submicron α-MoO3 freestanding channel, we
resolved ultraconfined PhPs with the record-high quality (Q) factor of up to 40 at room temperature, 2 times higher
than the previously reported highest value in α-MoO3. We further demonstrated PhPs guiding along a curved trajectory
and, for the first time, proved PhPs could be guided to desired angles
within spatially confined freestanding α-MoO3 channels.
The outcomes of this work can be exploited for creating high-Q PhP waveguides toward directional nanophotonic and polaritonic
devices.
“…This is clear evidence of geometric confinement, considering that, in RB3, numerically calculated Q factors from freestanding area (Figure a, red line) are slightly smaller than those from the supported area (Figure a, black line). The large Q factors of up to 40 in spatially confined freestanding α-MoO 3 is 2–4 times higher than previously reported values ,,, (see Table S1) in α-MoO 3 , even surpassing those obtained at the temperature as low as 50 K, where the temperature-dependent PhP damping is largely suppressed. Compared to the reduced temperature, submicron freestanding channels of hyperbolic materials presented in this work can be more conveniently realized and thus promising for real applications.…”
Section: Resultscontrasting
confidence: 58%
“…Within the x – y plane, hyperbolic PhPs propagate along the [001] and [100] directions in RB1 and RB2, respectively, and elliptic PhPs propagate in the x – y plane in RB3, resulting in anisotropic PhPs . The remarkably low loss of PhPs in α-MoO 3 , compared to counterparts such as boron nitride and graphene , can potentially lead to practical applications in IR signal processing and heat transfer . Due to strong crystallinity of each layer of α-MoO 3 , twistronics can also be readily experienced in this material. − Twisted double layer α-MoO 3 has been shown to be able to manipulate light at the nanoscale with topological transitions that bring huge potential to nanophotonics and polaritonics. − In addition to twisting the angle between adjacent α-MoO 3 layers, PhPs can also be engineered by other approaches, including patterning their microstructures, , changing the material composition, , and controlling the surrounding dielectric environment. , …”
Highly confined and in-plane anisotropic
phonon-polaritons (PhPs)
in orthorhombic-phase molybdenum trioxide (α-MoO3) exist in three Reststrahlen bands (RB) in the mid-infrared regime
where the crystal exhibits negative permittivity along three principal
axes. However, PhP behaviors in geometrically confined α-MoO3 remain enigmatic. Here, we investigated PhPs confined in
freestanding α-MoO3 covering submicron-width trenches.
We remarkably observed opposite trends in terms of PhP wavelengths
in two RBs for PhPs propagating on supported and spatially confined
freestanding α-MoO3. Due to the geometric confinement
in the submicron α-MoO3 freestanding channel, we
resolved ultraconfined PhPs with the record-high quality (Q) factor of up to 40 at room temperature, 2 times higher
than the previously reported highest value in α-MoO3. We further demonstrated PhPs guiding along a curved trajectory
and, for the first time, proved PhPs could be guided to desired angles
within spatially confined freestanding α-MoO3 channels.
The outcomes of this work can be exploited for creating high-Q PhP waveguides toward directional nanophotonic and polaritonic
devices.
“…[ 10 ] Also, confined electromagnetic waves coupled to phonons in hyperbolic dielectrics are referred to as hyperbolic phonon polaritons (HPhPs). [ 14 ] In particular, orthorhombic molybdenum trioxide (α‐MoO 3 ) [ 10b ] and vanadium pentoxide (α‐V 2 O 5 ) [ 10c ] have been demonstrated to support biaxial HPhPs with extreme anisotropy in the mid‐IR to terahertz spectral region (corresponding to energies ranging from molecular vibrations to thermal emission and absorption), which stems from their highly anisotropic lattice vibrations along different principal axes. In contrast to artificial surfaces, these natural hyperbolic two‐dimensional (2D) materials support higher wave vectors and electromagnetic confinement in the hyperbolic regime and, thus, offer potential advantages in planar focusing.…”
Manipulation of the propagation and energy‐transport characteristics of subwavelength infrared (IR) light fields is critical for the application of nanophotonic devices in photocatalysis, biosensing, and thermal management. In this context, metamaterials are useful composite materials, although traditional metal‐based structures are constrained by their weak mid‐IR response, while their associated capabilities for optical propagation and focusing are limited by the size of attainable artificial optical structures and the poor performance of the available active means of control. Herein, a tunable planar focusing device operating in the mid‐IR region is reported by exploiting highly oriented in‐plane hyperbolic phonon polaritons in α‐MoO3. Specifically, an unprecedented change of effective focal length of polariton waves from 0.7 to 7.4 μm is demonstrated by the following three different means of control: the dimension of the device, the employed light frequency, and engineering of phonon–plasmon hybridization. The high confinement characteristics of phonon polaritons in α‐MoO3 permit the focal length and focal spot size to be reduced to 1/15 and 1/33 of the incident wavelength, respectively. In particular, the anisotropic phonon polaritons supported in α‐MoO3 are combined with tunable surface‐plasmon polaritons in graphene to realize in situ and dynamical control of the focusing performance, thus paving the way for phonon‐polariton‐based planar nanophotonic applications.
“…Extension of these nonlinear effects to polaritonic modes [94][95][96] beyond those in graphene is a meaningful future direction. For example, monolayer hexagonal boron nitride [97,98] should exhibit strong second order optical nonlinearity due to broken inversion symmetry of the crystal lattice, and would be a natural platform for generating entanglement between the long lived hyperbolic phonon polaritons [99][100][101][102][103][104][105][106][107][108]. Similar nonlinear processes exist for optical phonons in SiC [109], Josephson plasmons in layered superconductors [110][111][112][113] and the collective modes in excitonic insulators [114][115][116][117][118].…”
Section: Discussion and Experimental Outlookmentioning
We analyze nonlinear optics schemes for generating pairs of quantum entangled plasmons in graphene. We predict that high plasmonic field concentration and strong optical nonlinearity of monolayer graphene enables pair-generation rates much higher than those of conventional photonic sources. The first scheme we study is spontaneous parametric down conversion in a graphene nanoribbon. In this second-order nonlinear process a plasmon excited by an external pump splits into a pair of plasmons, of half the original frequency each, emitted in opposite directions. The conversion is activated by applying a dc electric field that induces a density gradient or a current across the ribbon. Another scheme is degenerate four-wave mixing where the counter-propagating plasmons are emitted at the pump frequency. This third-order nonlinear process does not require a symmetrybreaking dc field. We suggest nano-optical experiments for measuring position-momentum entanglement of the emitted plasmon pairs. We estimate the critical pump fields at which the plasmon generation rates exceed their dissipation, leading to parametric instabilities.
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