Publications by authors named "Rockstuhl C"

Understanding the impact of the relativistic motion of a chiral molecule on its optical response is a prime challenge for fundamental science, but it also has a direct practical relevance in our search for extraterrestrial life. To contribute to these significant developments, we describe a multi-scale computational framework that combines quantum chemistry calculations and full-wave optical simulations to predict the chiral optical response from molecules moving at relativistic speeds. Specifically, the effect of a relativistic motion on the transmission circular dichroism (TCD) of three life-essential biomolecules, namely, B-DNA, chlorophyll a, and chlorophyll b, is investigated.

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Chiral materials are essential to perceive photonic devices that control the helicity of light. However, the chirality of natural materials is rather weak, and relatively thick films are needed for noticeable effects. To overcome this limitation, artificial photonic materials were suggested to affect the chiral response in a much more substantial manner.

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In the last few years, infrared reflection-absorption spectroscopy (IRRAS) has become a standard technique to study vibrational excitations of molecules. These investigations are strongly motivated by potential applications in monitoring chemical processes. For a better understanding of the adsorption mechanism of molecules on dielectrics, the polarization-dependence of an interaction of infrared light with adsorbates on dielectric surfaces is commonly used.

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Freeform dielectric waveguides connect optical chips made of different materials in fully integrated photonic devices. With a spatial extent in the order of 100 µm, they constitute a computational challenge and make Maxwell full-wave solvers unhandy for the accelerated design. Therefore, it is of utmost importance to have tools that permit the fast prediction of waveguide loss to enable the rapid optimization of waveguide trajectories.

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Nonlinear optics is essential for many recent photonic technologies. Here, a novel multi-scale approach is introduced to simulate the nonlinear optical response of molecular nanomaterials combining ab initio quantum-chemical and classical Maxwell-scattering computations. In this approach, the first hyperpolarizability tensor is computed with time-dependent density-functional theory and incorporated into a multi-scattering formalism that considers the optical interaction between neighboring molecules.

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Metasurfaces with bound states in the continuum (BICs) have proven to be a powerful platform for drastically enhancing light-matter interactions, improving biosensing, and precisely manipulating near- and far-fields. However, engineering metasurfaces to provide an on-demand spectral and angular position for a BIC remains a prime challenge. A conventional solution involves a fine adjustment of geometrical parameters, requiring multiple time-consuming calculations.

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Photonic time crystals are artificial materials whose electromagnetic properties are uniform in space but periodically vary in time. The synthesis of these materials and experimental observation of their physics remain very challenging because of the stringent requirement for uniform modulation of material properties in volumetric samples. In this work, we extend the concept of photonic time crystals to two-dimensional artificial structures-metasurfaces.

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Electroluminescence from single molecules adsorbed on a conducting surface imposes conflicting demands for the molecule-electrode coupling. To conduct electrons, the molecular orbitals need to be hybridized with the electrodes. To emit light, they need to be decoupled from the electrodes to prevent fluorescence quenching.

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Bianisotropic media can be used to engineer absorbance, scattering, polarization, and dispersion of electromagnetic waves. However, the demonstration of a tunable light-induced bianisotropy at optical frequencies is still lacking. Here, we propose an experimentally feasible concept for a light-induced tunable bianisotropic response in a homogeneous sphere made of an epsilon-near-zero (ENZ) material.

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Exploring the interaction of light with materials periodically structured in space and time is intellectually rewarding and, simultaneously, a computational challenge. Appropriate computational tools are urgently needed to explore how such upcoming photonic materials can control light on demand. Here, we introduce a semi-analytical approach based on the transition matrix (also known as T-matrix) to analyze the optical response of a spatiotemporal metasurface.

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Solving the inverse problem is a major challenge in contemporary nano-optics. However, frequently not just a possible solution needs to be found but rather the solution that accommodates constraints imposed by the problem at hand. To select the most plausible solution for a nano-optical inverse problem additional information can be used in general, but how to specifically formulate it frequently remains unclear.

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The design of scatterers on demand is a challenging task that requires the investigation and development of novel and flexible approaches. In this paper, we propose a machine learning-assisted optimization framework to design multi-layered core-shell particles that provide a scattering response on demand. Artificial neural networks can learn to predict the scattering spectrum of core-shell particles with high accuracy and can act as fully differentiable surrogate models for a gradient-based design approach.

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Multi-photon lithography allows us to complement planar photonic integrated circuits (PIC) by in-situ 3D-printed freeform waveguide structures. However, design and optimization of such freeform waveguides using time-domain Maxwell's equations solvers often requires comparatively large computational volumes, within which the structure of interest only occupies a small fraction, thus leading to poor computational efficiency. In this paper, we present a solver-independent transformation-optics-(TO-) based technique that allows to greatly reduce the computational effort related to modeling of 3D freeform waveguides.

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The modeling of functional photonic devices that rely on molecular materials continues to be a major contemporary challenge. It is a challenge because, in the Maxwell equations, which govern the light-matter interaction, material properties are primarily introduced on phenomenological grounds and not from first principles. To overcome such limitations, we outline a multiscale modeling approach that bridges multiple length scales.

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Graphene flakes acting as photonic nanoantennas may sustain strong electromagnetic field localization and enhancement. To exploit the field enhancement, quantum emitters such as atoms or molecules should be positioned in such close proximity to the flake that electron tunneling might influence the optical and electronic properties of the system. However, tunneling is usually not considered if the optical coupling mechanism between quantum emitters and nanoantennas is at focus.

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Liquid crystalline (LC) dimers formed helical nanofilaments depending on the parity of the alkyl linker, revealing an unusual odd-even effect. Molecular dynamics simulations were used to investigate the observed tendency. Elongation of the linker translates to an increase of the pitch of the helices, which allows achieving tuneable helical assemblies of Au nanoparticles doped to the LC matrix.

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The recent fabrication advances in nanoscience and molecular materials point toward a new era where material properties are tailored in silico for target applications. To fully realize this potential, accurate and computationally efficient theoretical models are needed for: a) the computer-aided design and optimization of new materials before their fabrication; and b) the accurate interpretation of experiments. The development of such theoretical models is a challenging multi-disciplinary problem where physics, chemistry, and material science are intertwined across spatial scales ranging from the molecular to the device level, that is, from ångströms to millimeters.

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We investigate molecular plasmonic excitations sustained in hollow spherical gold nanoparticles using time-dependent density functional theory (TD-DFT). Specifically, we consider Au spherical, hollow molecules as a toy model for single-shell plasmonic molecules. To quantify the plasmonic character of the excitations obtained from TD-DFT, the energy-based plasmonicity index is generalized to the framework of DFT, validated on simple systems such as the sodium Na chain and the silver Ag compound, and subsequently successfully applied to more complex molecules.

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While various nanophotonic structures applicable to relatively thin crystalline silicon-based solar cells were proposed to ensure effective light in-coupling and light trapping in the absorber, it is of great importance to evaluate their performance on the solar module level under realistic irradiation conditions. Here, we analyze the annual energy yield of relatively thin (crystalline silicon (c-Si) wafer thickness between 5 μm and 80 μm) heterojunction (HJT) solar module architectures when optimized anti-reflective and light trapping titanium dioxide (TiO) nanodisk square arrays are applied on the front and rear cell interfaces, respectively. Our numerical study shows that upon reducing c-Si wafer thickness down to 5 μm, the relative increase of the annual energy yield can go up to 23.

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We propose using deep neural networks for the fast retrieval of effective properties of metamaterials based on their angular-dependent reflection and transmission spectra from thin slabs. While we noticed that non-uniqueness is an issue for a successful application, we propose as a solution an automatic algorithm to subdivide the entire parameter space. Then, in each sub-space, the mapping between the optical response (complex reflection and transmission coefficients) and the corresponding material parameters (dielectric permittivity and permeability) is unique.

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Conventional optical diffusers, such as thick volume scatterers (Rayleigh scattering) or microstructured surface scatterers (geometric scattering), lack the potential for on-chip integration and are thus incompatible with next-generation photonic devices. Dielectric Huygens' metasurfaces, on the other hand, consist of 2D arrangements of resonant dielectric nanoparticles and therefore constitute a promising material platform for ultrathin and highly efficient photonic devices. When the nanoparticles are arranged in a random but statistically specific fashion, diffusers with exceptional properties are expected to come within reach.

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Liquid-phase, quasi-epitaxial growth is used to stack asymmetric, dipolar organic compounds on inorganic substrates, permitting porous, crystalline molecular materials that lack inversion symmetry. This allows material fabrication with built-in electric fields. A new programmed assembly strategy based on metal-organic frameworks (MOFs) is described that facilitates crystalline, noncentrosymmetric space groups for achiral compounds.

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Optimal light absorption is decisive in obtaining high-efficiency solar cells. An established, if not to say the established, approach is to texture the interface of the light-absorbing layer with a suitable microstructure. However, structuring the light-absorbing layer is detrimental concerning its electrical properties due to an increased surface recombination rate (owing to enlarged surface area and surface defects) caused by the direct patterning process itself.

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