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In this work we derive the state of strain or stress under symmetry conserving conditions in pseudomorphic lattices with monoclinic symmetry. We compare surface vectors across the template epitaxial layer interface and impose conditions of a stress free epitaxial layer. As a result, we demonstrate the existence, in theory, of exactly three possible unit cells which can establish onto a given template. We demonstrate this approach for a class of templates with $(h0l)$ planes and $\beta$-(Al$_x$Ga$_{1-x}$)$_2$O$_3$ on $(h0l)$ $\beta$-Ga$_2$O$_3$. We discuss the effects of composition $x$ and surface orientation onto the formation of three elastically stable unit cells, their strain and stress tensors, unit cell axes, unit cell volumes, lattice spacing, elastic potential energies, and stress free directions. The previous paradigm for epitaxial layer growth where the stress free direction is always perpendicular to the growing surface is not generally valid for low symmetry materials. In the example here, we find two possible competing domains with stress free direction oblique to the surface of the template for almost all planes $(h0l)$. We calculate the band-to-band transitions for $\beta$-(Al$_{0.1}$Ga$_{0.9}$)$_2$O$_3$ on $(h0l)$ $\beta$-Ga$_2$O$_3$ using the composition dependent deformation parameters and elastic coefficients reported prevoiously [Korlacki~\textit{et al.} Phys. Rev. Appl.~\textbf{18}, 064019 (2022)]., Comment: 10 pages, 8 figures

In this letter, we derive an expression for magnetic dipole transitions that is analogous to the Lyddane-Sachs-Teller relation for dielectric polar lattice vibrations. We thereby define transverse and longitudinal optical frequencies at which paramagnetic resonance and antiresonance occurs, respectively. The relation found here thus permits non-invasive optical analysis of static magnetization properties in paramagnetic materials. Validated through terahertz electron paramagnetic resonance ellipsometry and superconducting quantum interference device measurements on Iron-doped Gallium Nitride, our findings show very good agreement between theory and experiment. We term the excitations associated with the paramagnetic transitions as paramagnetic polaritons which may find use in future photonic applications

A generalized approach derived from Blochs equation of motion of nuclear magnetic moments is presented to model the frequency, magnetic field, spin density, and temperature dependencies in the electromagnetic permeability tensor for materials with magnetic resonances. The resulting tensor model predicts characteristic polarization signatures which can be observed, for example, in fully polarization-resolved Mueller matrix element spectra measured across magnetic resonances as a function of frequency, magnetic field, magnetic moment density, and temperature. When augmented with thermodynamic considerations and suitable Hamiltonian description of the magnetic eigenvalue spectrum, important parameters such as zero-frequency magnetization, spectral amplitude distribution, relaxation time constants, and geometrical orientation parameters of the magnetic moment density can be obtained from comparing the generalized model approach to experimental data. We demonstrate our approach by comparing model calculations with full Mueller matrix element spectra measured at oblique angle of incidence in the terahertz spectral range, across electron spin resonance quintuplet transitions observed in wurtzite-structure GaN doped with iron. Measurements were performed by ellipsometry, using a superconducting cryostat magnet at magnetic fields of 7.23 T and at temperatures of 20 K and 30 K. We detail the occurrence of linear and circular birefringence and dichroism associated with each of the zero-field split spin transitions in the S = 5/2 defect system. We derive the spectral dependence of the magnetic susceptibility function and obtain the temperature and magnetic field dependence of the spin Hamiltonian. Our model correctly predicts the complexity of the polarization signatures observed in the 15 independent elements of the normalized Mueller matrix for both positive and negative magnetic fields.

Monoclinic $\beta$-Ga$_2$O$_3$ films grown on $c$-plane sapphire have been shown to exhibit six $(\bar{2}01)$-plane oriented domains, which are equally-spaced-by-rotation around the surface normal and equally-sized-by-volume that render the film optical response effectively uniaxial. We derive and discuss an optical model suitable for ellipsometry data analysis of such films. We model mid- and far-infrared ellipsometry data from undoped and electrically insulating films with an effective uniaxial dielectric tensor based on projections of all phonon modes within the rotation domains parallel and perpendicular to the sample normal, i.e., to the reciprocal lattice vector $\mathbf{g}_{\bar{2}01}$. Two effective response functions are described by model, and found sufficient to calculate ellipsometry data that best-match measured ellipsometry data from a representative film. We propose to render either effective dielectric functions, or inverse effective dielectric functions, each separately for electric field directions parallel and perpendicular to $\mathbf{g}_{\bar{2}01}$, by sums of Lorentz oscillators, which permit to determine either sets of transverse optical phonon mode parameters, or sets of longitudinal optical phonon mode parameters, respectively. Transverse optical modes common to both dielectric functions can be traced back to single crystal modes with $B_{\mathrm{u}}$ character, while modes with $A_{\mathrm{u}}$ character only appear within the dielectric function for polarization perpendicular to the sample surface. The thereby obtained parameter sets reveal all phonon modes anticipated from averaging over the six-fold rotation domains of single crystal $\beta$-Ga$_2$O$_3$, but with slightly shifted transverse optical, and completely different longitudinal optical phonon modes., Comment: 14 pgaes, 8 figures

Nitrogen-polar III-nitride heterostructures offer advantages over metal-polar structures in high frequency and high power applications. However, polarity control in III-nitrides is difficult to achieve as a result of unintentional polarity inversion domains (IDs). Herein, we present a comprehensive structural investigation with both atomic detail and thermodynamic analysis of the polarity evolution in low- and high-temperature AlN layers on on-axis and 4$^{\circ}$ off-axis Carbon-face 4H-SiC (000$\bar{1}$) grown by hot-wall metal organic chemical vapor deposition. A polarity control strategy has been developed by variation of thermodynamic Al supersaturation and substrate misorientation angle in order to achieve desired growth mode and polarity. We demonstrate that IDs are totally suppressed for high-temperature AlN nucleation layers when step-flow growth mode is achieved at the off-axis. We employ this approach to demonstrate high quality N-polar epitaxial AlGaN/GaN/AlN heterostructures., Comment: 9 pages, 6 figures

The bowing of the energy of the three lowest band-to-band transitions in $\beta$-(Al$_{x}$Ga$_{1-x}$)$_2$O$_3$ alloys was resolved using a combined density functional theory (DFT) and generalized spectroscopic ellipsometry (GSE) approach. The DFT calculations of the electronic band structure of both, $\beta$-Ga$_2$O$_3$ and $\theta$-Al$_2$O$_3$, allow extracting of the linear portion of the energy shift in the alloys, and provide a method for quantifying the role of coherent strain present in the $\beta$-(Al$_{x}$Ga$_{1-x}$)$_2$O$_3$ thin films on (010) $\beta$-Ga$_2$O$_3$ substrates. The energies of band-to-band transitions were obtained using the spectroscopic ellipsometry eigenpolarization model approach [A. Mock et al., Phys. Rev. B 95, 165202 (2017)]. After subtracting the effects of strain which also induces additional bowing and after subtraction of the linear portion of the energy shift due to alloying, the bowing parameters associated with the three lowest band-to-band transitions in monoclinic $\beta$-(Al$_{x}$Ga$_{1-x}$)$_2$O$_3$ are found., Comment: 12 pages, 5 figures

Metalorganic chemical vapor deposition (MOCVD) of GaN layers doped with Mg atoms to the recognized optimum level of [Mg] $\sim2 \times 10^{19}$ cm$^{-3}$ has been performed. In a sequence of MOCVD runs, operational conditions, including temperature and flow rate of precursors, have been maintained except for intentionally larger flows of hydrogen carrier gas fed into the reactor. By employing the largest hydrogen flow of 25 slm in this study, the performance of the as-grown Mg-doped GaN layers has been certified by a room-temperature hole concentration of $p\sim2 \times 10^{17}$ cm$^{-3}$ in the absence of any thermal activation treatment. Experimental evidence is delivered that the large amounts of hydrogen during the MOCVD growth can regulate the incorporation of the Mg atoms into GaN in a significant way so that MgH complex can co-exist with a dominant and evidently electrically active isolated MgGa acceptor., Comment: 11 pages, 3 figures

The hot-wall metal-organic chemical vapor deposition (MOCVD), previously shown to enable superior III-nitride material quality and high performance devices, has been explored for Mg doping of GaN. We have investigated the Mg incorporation in a wide doping range ($2.45\times{10}^{18}~cm^{-3}$ up to $1.10\times{10}^{20}~cm^{-3}$) and demonstrate GaN:Mg with low background impurity concentrations under optimized growth conditions. Dopant and impurity levels are discussed in view of Ga supersaturation which provides a unified concept to explain the complexity of growth conditions impact on Mg acceptor incorporation and compensation. The results are analysed in relation to the extended defects, revealed by scanning transmission electron microscopy (STEM), X-ray diffraction (XRD), and surface morphology, and in correlation with the electrical properties obtained by Hall effect and capacitance-voltage (C-V) measurements. This allows to establish a comprehensive picture of GaN:Mg growth by hot-wall MOCVD providing guidance for growth parameters optimization depending on the targeted application. We show that substantially lower H concentration as compared to Mg acceptors can be achieved in GaN:Mg without any in-situ or post-growth annealing resulting in p-type conductivity in as-grown material. State-of-the-art $p$-GaN layers with a low-resistivity and a high free-hole density (0.77 $\Omega$.cm and $8.4\times{10}^{17}~cm^{-3}$, respectively) are obtained after post-growth annealing demonstrating the viability of hot-wall MOCVD for growth of power electronic device structures., Comment: main: 11 pages, 8 figures - supplementary: 2 pages, 3 figures

We report on terahertz (THz) electron paramagnetic resonance generalized spectroscopic ellipsometry (THz-EPR-GSE). Measurements of the field and frequency dependencies of the magnetic response due to the spin transitions associated with the nitrogen defect in 4H-SiC are shown as an example. THz-EPR-GSE dispenses with the need of a cavity, permits independently scanning field and frequency parameters, and does not require field or frequency modulation. We investigate spin transitions of hexagonal ($h$) and cubic ($k$) coordinated nitrogen including coupling with its nuclear spin (I=1), and we propose a model approach for the magnetic susceptibility to account for the spin transitions. From the THz-EPR-GSE measurements we can fully determine the polarization properties of the spin transitions and we obtain $g$ and hyperfine splitting parameters using magnetic field and frequency dependent Lorentzian oscillator lineshape functions. We propose frequency-scanning THz-EPR-GSE as a new and versatile method to study properties of spins in solid state materials., Comment: 6 pages, 5 figures

We determine the anisotropic dielectric functions of rhombohedral $\alpha$-Ga$_2$O$_3$ by far-infrared and infrared generalized spectroscopic ellipsometry and derive all transverse optical and longitudinal optical phonon mode frequencies and broadening parameters. We also determine the high frequency and static dielectric constants. We perform density functional theory computations and determine the phonon dispersion for all branches in the Brillouin zone, and we derive all phonon mode parameters at the Brillouin zone center including Raman-active, infrared-active, and silent modes. Excellent agreement is obtained between our experimental and computation results as well as among all previously reported partial information from experiment and theory. We also compute the same information for $\alpha$-Al$_2$O$_3$, the binary parent compound for the emerging alloy of $\alpha$-(Al$_{x}$Ga$_{1-x}$)$_2$O$_3$, and use results from previous investigations [Schubert, Tiwald, and Herzinger, Phys. Rev. B 61, 8187 (2000)] to compare all properties among the two isostructural compounds. From both experimental and theoretical investigations we compute the frequency shifts of all modes between the two compounds. Additionally, we calculate overlap parameters between phonon mode eigenvectors and discuss the possible evolution of all phonon modes into the ternary alloy system and whether modes may form single mode or more complex mode behaviors.

Nanostructures of conventional metals offer manipulation of light at the nanoscale but are limited to static behavior due to their fixed material properties. To develop the next frontier of dynamic nanooptics and metasurfaces, we utilize the redox-tunable optical properties of conducting polymers, which were recently shown to be capable of sustaining plasmons in their most conducting oxidized state. Using nanodisks of poly(3,4-ethylenedioxythiophene:sulfate) (PEDOT:Sulf) as a model system, we present the first electrically tunable conducting polymer nanooptical antennas. In addition to repeated on/off switching of the polymeric nanoantennas, we demonstrate the possibility for gradual electrical tuning of their nanooptical response, which was found to be related to the modulation of both density and mobility of the mobile polaronic charge carriers in the polymer. The presented concept takes important steps towards electrically tunable metasurfaces with truly dynamic optical nanoantenna pixels, with not only varying farfield but also tunable nearfield. The work paves the way for applications ranging from tunable flat metaoptics to adaptable smart windows.

A complete set of all optical phonon modes predicted by symmetry for bixbyite structure indium oxide is reported here from a combination of far-infrared and infrared spectroscopic ellipsometry, as well as first principle calculations. Dielectric function spectra measured on high quality, marginally electrically conductive melt grown single bulk crystals are obtained on a wavelength-by-wavelength (a.k.a. point-by-point) basis and by numerical reduction of a subtle free charge carrier Drude model contribution. A four-parameter semi-quantum model is applied to determine all sixteen pairs of infrared-active transverse and longitudinal optical phonon modes, including the high-frequency dielectric constant, $\varepsilon_{\infty}=4.05\pm 0.05$. The Lyddane-Sachs-Teller relation then gives access to the static dielectric constant, $\varepsilon_{\mathrm{DC}}=10.55\pm 0.07$. All experimental results are in excellent agreement with our density functional theory calculations and with previously reported values, where existent. We also perform optical Hall effect measurements and determine for the unintentionally doped $n$-type sample a free electron density of $n=(2.81 \pm 0.01)\times 10^{17}$~cm$^{-3}$, mobility of $\mu=(112 \pm 3)$~cm$^{2}$/(Vs), and an effective mass parameter of $(0.208\pm0.006)m_e$. Density and mobility parameters compare very well with results of electrical Hall effect measurements. Our effective mass parameter, which is measured independently of any other experimental technique, represents the bottom curvature of the $\Gamma$ point in In$_2$O$_3$ in agreement with previous extrapolations. We use terahertz spectroscopic ellipsometry to measure the quasi-static response of In$_2$O$_3$, and our model validates the static dielectric constant obtained from the Lyddane-Sachs-Teller relation.

Precise manipulation of light-matter interaction has enabled a wide variety of approaches to create bright and vivid structural colours. Techniques utilizing photonic crystals, Fabry-P\'erot cavities, plasmonics, or high-refractive index dielectric metasurfaces have been studied for applications ranging from optical coatings to reflective displays. However, complicated fabrication procedures for sub-wavelength nanostructures, limited active areas, and inherent absence of tunability with these approaches significantly impede their further developments towards flexible, large-scale, and switchable devices compatible with facile and cost-effective production. Herein, we present a way to generate structural colours based on conducting polymer thin films prepared on metallic surfaces via vapour phase polymerization and ultraviolet (UV) light patterning. Varying the UV dose leads to synergistic variation of film absorption and thickness, which generates controllable colours from violet to red. Together with greyscale photomasks this enables fabrication of high-resolution colour images using single exposure steps. We further demonstrate spatiotemporal tuning of the structurally coloured surfaces and images via electrochemical modulation of the polymer redox state. The simple structure, facile fabrication, wide colour gamut, and dynamic colour tuning make this concept competitive for future multi-functional and smart displays.

Presented here is the development and demonstration of a tunable cavity-enhanced terahertz frequency-domain optical Hall effect technique. The cavity consists of at least one fixed and one tunable Fabry-P\'erot resonator. The approach is suitable for enhancement of the optical signatures produced by the optical Hall effect in semi-transparent conductive layer structures with plane parallel interfaces. The physical principle is the constructive interference of electric field components that undergo multiple optical Hall effect induced polarization rotations upon multiple light passages through the conductive layer stack. Tuning one of the cavity parameters, such as the external cavity thickness, permits shifting of the frequencies of the constructive interference, and enhancement of the optical signatures produced by the optical Hall effect can be obtained over large spectral regions. A cavity-tuning optical stage and gas flow cell are used as examples of instruments that exploit tuning an external cavity to enhance polarization changes in a reflected terahertz beam. Permanent magnets are used to provide the necessary external magnetic field. Conveniently, the highly reflective surface of a permanent magnet can be used to create the tunable external cavity. The signal enhancement allows the extraction of the free charge carrier properties of thin films, and can eliminate the need for expensive super-conducting magnets. Furthermore, the thickness of the external cavity establishes an additional independent measurement condition, similar to, for example, the magnetic field strength, terahertz frequency, and angle of incidence. A high electron mobility transistor structure and epitaxial graphene are studied as examples. We discuss the theoretical background, instrument design, data acquisition, and data analysis procedures., Comment: 12 pages, 8 figures

Polymer based stereolithographic additive manufacturing has been established for the rapid and low-cost fabrication of THz optical components due to its ability to construct complex 3D geometries with high resolution. For polymer based or integrated optics, thermal annealing processes are often used to optimize material properties. However, despite the growing interest in THz optics fabricated using stereolithography, the effects of thermal annealing on the THz dielectric properties of polymethacrylates compatible with stereolithography has not been studied yet. In this manuscript we report on the THz ellipsometric response of thermally annealed polymethacrylates prepared using UV polymerization. Our findings indicate that the investigated polymethacrylate maintain a stable optical response in THz spectral range from 650 to 950 GHz after thermal annealing at temperatures up to 70 degrees C for several hours.

Metal nanostructures are key elements in nanooptics owing to their strong resonant interaction with light through local plasmonic charge oscillations. Their ability to shape light at the nanoscale have made them important across a multitude of areas, including biosensing, energy conversion and ultrathin flat metaoptics. Yet another dimension of avenues is foreseen for dynamic nanoantennas, ranging from tuneable metalenses for miniaturized medical devices to adaptable windows that control radiation flows in and out of buildings. However, enabling nano-optical antennas to be dynamically controllable remains highly challenging and particularly so for traditional metals with fixed permittivity. Here we present state-of-the-art conductive polymers as a new class of organic plasmonic materials for redox-tuneable nano-optics. Through experiments and simulations, we show that nanodisks of highly conductive polymers can provide clear optical extinction peaks via excitation of dipolar localised surface plasmon resonances. Resonance frequencies redshift with increasing nanodisk aspect ratio, in agreement with analytical calculations based on dipolar polarizability theory. We furthermore demonstrate complete switching of the optical response of the organic nanoantennas by chemical tuning of the polymer's redox state, which effectively modulates the material permittivity between plasmonic and non-plasmonic regimes. Our results thereby show that conductive polymer nanostructures can act as redox-tuneable plasmonic nanoantennas, based on bipolaronic charge carriers rather than electrons as in conventional metals. Future directions may investigate different polymers and geometries to further widen the plasmonic spectral range (here around 0.8 to 3.6 {\mu}m) as well as different ways of tuning.

We present a terahertz (THz) frequency-domain spectroscopic (FDS) ellipsometer design which suppresses formation of standing waves by use of stealth technology approaches. The strategy to suppress standing waves consists of three elements \textit{geometry}, \textit{coating} and \textit{modulation}. The instrument is based on the rotating analyzer ellipsometer principle and can incorporate various sample compartments, such as a superconducting magnet, \textit{in-situ} gas cells or resonant sample cavities, for example. A backward wave oscillator and three detectors are employed, which permit operation in the spectral range of 0.1--1~THz (3.3--33~cm$^{-1}$ or 0.4--4~meV). The THz frequency-domain ellipsometer allows for standard and generalized ellipsometry at variable angles of incidence in both reflection and transmission configurations. The methods used to suppress standing waves and strategies for an accurate frequency calibration are presented. Experimental results from dielectric constant determination in anisotropic materials, and free charge carrier determination in optical Hall effect, resonant-cavity enhanced optical Hall effect and \textit{in-situ} optical Hall effect experiments are discussed. Examples include silicon and sapphire optical constants, free charge carrier properties of two dimensional electron gas in group-III nitride high electron mobility transistor structure, and ambient effects on free electron mobility and density in epitaxial graphene.

Mid-infrared optical Hall effect measurements are used to determine the free charge carrier parameters of an unintentionally doped wurtzite-structure $c$-plane oriented In$_{0.33}$Ga$_{0.67}$N epitaxial layer. Room temperature electron effective mass parameters of $m^{*}_{\bot}=(0.205 \pm 0.013)~m_0$ and $m^{*}_{\parallel}=(0.204 \pm 0.016)~m_0$ for polarization perpendicular and parallel to the $c$-axis, respectively, were determined. The free electron concentration was obtained as $(1.7 \pm 0.2)\times 10^{19}~$cm$^{-3}$. Within our uncertainty limits we detect no anisotropy for the electron effective mass parameter and we estimate the upper limit of the possible effective mass anisotropy is 7$\%$. We discuss the influence of band nonparabolicity on the electron effective mass parameter as a function of In content. The effective mass parameter is consistent with a linear interpolation scheme between the conduction band mass parameters in GaN and InN when the strong nonparabolicity in InN is included. The In$_{0.33}$Ga$_{0.67}$N electron mobility parameters were found to be anisotropic supporting previous experimental findings for wurtzite-structure GaN, InN, and Al$_{x}$Ga$_{1-x}$N epitaxial layers with $c$-plane growth orientation., Comment: 5 pages, 3 figures, 1 table

The isotropic average conduction band minimum electron effective mass in Sn-doped monoclinic single crystal $\beta$-Ga$_2$O$_3$ is experimentally determined by mid-infrared optical Hall effect to be $(0.284\pm0.013)m_{0}$ combining investigations on ($010$) and ($\bar{2}01$) surface cuts. This result falls within the broad range of values predicted by theoretical calculations for undoped $\beta$-Ga$_2$O$_3$. The result is also comparable to recent density functional calculations using the Gaussian-attenuation-Perdue-Burke-Ernzerhof hybrid density functional, which predict an average effective mass of $0.267m_{0}$ (arXiv:1704.06711 [cond-mat.mtrl-sci]). Within our uncertainty limits we detect no anisotropy for the electron effective mass, which is consistent with most previous theoretical calculations. We discuss upper limits for possible anisotropy of the electron effective mass parameter from our experimental uncertainty limits, and we compare our findings with recent theoretical results.

We present a comprehensive study of the band structure of two- and three-dimensional hexagonal layered materials using Landau Level optical Hall effect spectroscopy investigations, employing graphene and graphite as model systems. We study inter-Landau-level transitions in highly oriented pyrolytic graphite and a stack of multilayer graphene on C-face 6\textit{H}-SiC, using data from reflection-type optical Hall effect measurements in the mid-infrared spectral range at sample temperatures of $T=1.5$~K and magnetic fields up to $B=8$~T. We describe a comprehensive dielectric polarizability model for inter-Landau-level transitions, which permits analysis of the optical Hall effect data. From their magnetic field dependence we identify sets of H- and K-point inter-Landau-level transitions in graphite and sets of inter-Landau-level transition from decoupled graphene single, and coupled graphene bi-, tri-, and quad-layer for the multilayer graphene stack. For inter-Landau-level transitions in decoupled graphene single-layers and H-point transitions in graphite we observe polarization mode preserving behavior, requiring symmetric magneto-optical contributions to the corresponding dielectric tensors. Inter-Landau-level transitions in coupled graphene layers as well as K-point transitions in graphite exhibit polarization mode mixing behavior, requiring antisymmetric magneto-optical contributions to the corresponding dielectric tensors. From the circular-polarization-averaged inter-Landau-level transition energies and the energy splitting between right- and left-handed circular polarized inter-Landau-level transitions we determine the model parameters in the Slonczewski-Weiss-McClure band structure approximation for two- and three-dimensional hexagonal layered materials, with graphene and graphite as examples.

We employ an eigen polarization model including the description of direction dependent excitonic effects for rendering critical point structures within the dielectric function tensor of monoclinic \beta-Ga2O3 yielding a comprehensive analysis of generalized ellipsometry data obtained from 0.75 eV--9 eV. The eigen polarization model permits complete description of the dielectric response, and we obtain single-electron and excitonic band-to-band transition anisotropic critical point structure model parameters including their polarization eigenvectors within the monoclinic lattice. We compare our experimental analysis with results from density functional theory calculations performed using a recently proposed Gaussian-attenuation-Perdue-Burke-Ernzerhof hybrid density functional, and we present and discuss the order of the fundamental direct band-to-band transitions and their polarization selection rules, the electron and hole effective mass parameters for the three lowest band-to-band transitions, and their exciton binding energy parameters, in excellent agreement with our experimental results. We find that the effective masses for holes are highly anisotropic and correlate with the selection rules for the fundamental band-to-band transitions, where the observed transitions are polarized closely in the direction of the lowest hole effective mass for the valence band participating in the transition.