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Marcel Schubert

Publications and source records attributed to Marcel Schubert.

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Purely equatorial lasing in spherical liquid crystal polymer microlasers with engineered refractive index gradient

Liquid crystal whispering gallery mode microlasers show high sensitivity to external stimuli and distinct spectral features, rendering them ideally suited for various sensing applications. They also offer intrinsic anisotropic optical properties, which can be used to shape and manipulate light even inside spatially highly symmetric structures. Here, we report the synthesis and detailed optical characterization of a spherical bipolar liquid crystal polymer microlaser that tightly confines the optical path of whispering gallery modes to the equatorial plane. By controlled anchoring of the liquid crystal mesogens followed by polymerization, a fixed refractive index gradient is formed within the spherical microcavity. Consequently, only transverse electric (TE) modes oscillating in the equatorial plane experience the high extraordinary refractive index, allowing to confine lasing into a single plane. Furthermore, we observe that the refractive index gradient causes a characteristic splitting of the TE modes. By combining hyperspectral imaging and analytical modeling, we demonstrate that the observed splitting is caused by lifting of the energy degeneracy of higher order azimuthal laser modes, enabling direct insights into the complex interplay of refractive index gradients and resulting whispering gallery mode confinement. In addition, the unique ability to confine lasing of a spherical microbead into only a single plane makes these microlasers independent of the exact position of the pump beam, which allows consistent localized sensing especially in combination with fast point scanning microscopes or inside highly dynamic biological environments.

physics.optics

Minimal-footprint photonic crystal nanolasers for biointegration

Photonic crystals allow unprecedented control over how light is confined, propagates, and interacts with matter. Their development has had a transformative impact on optics and physics, and they remain the central platform for both fundamental discoveries and practical photonic technologies. However, the relatively large footprint and substrate-bound nature of photonic crystal structures have so far strongly limited their use as miniature optical devices or biointegrated sensors. Here, we overcome these limitations by identifying the minimal size of a 2D photonic crystal array needed to achieve lasing and describe the fabrication of substrate-less hexagonal laser particles with an active area as small as 30 {\mu}m2. Massively parallel fabrication, robust detachment, and integration of the nanolaser particles into live cells is demonstrated. Crucially, by engineering spatial and spectral mode characteristics, we designed NIR-II probes with mode volumes on the order of tens of attolitres, an order of magnitude smaller than whispering gallery probes of similar dimensions. Such high light localization is comparable in scale to different organelles of eucaryotic cells. In the future, we expect that chemical or plasmonic functionalization of the device will enable label-free sensing of nanoscale intracellular processes, and that it shall serve as a miniature platform to exploit developments in optical and quantum sensing for chemical and biological applications.

physics.optics

Elastomer-based whispering gallery mode microlasers with low Young's modulus for biosensing applications

Sensing biological forces with microscopic lasers is an emerging technique that offers significant advantages over conventional fluorescent probes and imaging-based techniques. However, the limited availability of suitable deformable or elastic microlaser materials is restricting the scale of forces that can be detected which strongly narrows their overall applicability. Here, we describe the synthesis of spherical whispering gallery mode microbead lasers from a commercially available elastomer material in a microfluidic system with high viscosity. Upon doping with an organic dye, the microbeads show multimode lasing with thresholds in the range of 2-11 nJ. Measurements of the mechanical properties reveal that the width of the laser modes is directly proportional to the applied external force. The measured mean Young's modulus is 36 kPa, comparable to the stiffness of single cells and soft tissues. We also demonstrate that elastomer microlasers are stable under cell culture conditions for several days and observe splitting of the laser modes for intracellular microlasers. The observed properties render elastomer microlasers as a robust material platform for biointegrated lasers that also allows further tuning of the mechanical and optical properties for tailored force sensing inside cells, tissues, and small animals.

physics.optics

Monitoring microplastics in live reef-building corals with microscopic laser particles

Micro- and nanoplastics pose a growing threat to marine organisms, such as reef-building corals. Yet, our understanding of microplastic uptake, interaction with coral tissue, and incorporation into coral skeletons remains limited, mainly due to the invasiveness of existing methods for detecting microplastics. Here, we exploit optical resonances in polymer spheres to transform microplastic particles into microscopic lasers. The bright, distinctive, and stable spectral signatures emitted by the microscopic laser particles function as optical barcodes, allowing extended tracking of microplastics transport through optically opaque coral tissue. Simultaneously, the lasers provide real-time sensing of dynamic changes at the microplastic surface with nanoscale resolution. Using confocal hyperspectral imaging, we establish the technical and analytical framework to capture coral anatomy and combine tracking and surface sensing into an integrated, non-invasive approach. With this, we explore the transport and internalization of individual microplastics in live corals, opening new avenues for understanding their ecological impact.

physics.bio-ph

DNA Sensing with Whispering Gallery Mode Microlasers

Nucleic acid sensing is crucial for advancing diagnostics, therapeutic monitoring and molecu-lar biology research, by enabling the precise identification of DNA and RNA interactions. Here, we present an innovative sensing platform based on DNA-functionalized whispering gallery mode (WGM) microlasers. By correlating spectral shifts in laser emission to changes in refractive index, we demonstrate real-time detection of DNA hybridization and structural changes. The addition of gold nanoparticles to the DNA strands significantly enhances sensi-tivity, and labeling exclusively the sensing strand or a hairpin strand eliminates the need for secondary labeling of the target strand. We further show that ionic strength influences DNA compactness, and we introduce a hairpin-based system as a dual-purpose sensor and con-trolled release mechanism for potential drug delivery. This versatile WGM-based platform of-fers promise for sequence-specific nucleic acid sensing, multiplexed detection, and in vivo ap-plications in diagnostics and cellular research.

physics.optics

Optically manipulated micromirrors for precise excitation of WGM microlasers

Whispering gallery mode microlasers are highly sensitive refractive index sensors widely explored for biophotonic and biomedical applications. Microlaser excitation and collection of the emitted light typically utilize microscope objectives at normal incidence, limiting the choice of the oscillation plane of the modes. Here, we present a platform that enables the excitation of microlasers from various directions using an optically manipulated micromirror. The scheme enables precise sensing of the environment surrounding the microlasers along different well-controlled planes. We further demonstrate the capability of the platform to perform a time-resolved experiment of dynamic sensing using a polystyrene probe bead orbiting the microlaser.

physics.optics

Local sensing of absolute refractive index during protein-binding using microlasers with spectral encoding

Multiplexed, specific and sensitive detection of antigens is critical for the rapid and accurate diagnosis of disease and the informed development of personalized treatment plans. Here, we show that polymer microsphere lasers can be used as photonic sensors to monitor and quantify direct surface binding of biomolecules via changes in the refractive index. The unique spectral signature of each individual laser can be used to find their size and effective refractive index which adds a new encoding dimension when compared to conventional fluorescent beads. We utilize antibody-functionalized microlasers to selectively detect protein binding. Different stages of the multilayer surface modification can be resolved, and protein binding is demonstrated for two different proteins, IgG and CRP. Moreover, by continuously monitoring single lasers, we demonstrate the possibility of real-time monitoring of binding dynamics between antigens in solution phase and the immobilized antibodies. For multiplexed detection, the microlasers are employed in a flow cytometer configuration, with fast spectral detection and identification of microlasers with and without antigen binding. We envision that by combining microlasers with well-established surface modification chemistries and flow geometries, the multiplexing ability of microbead immunoassays can be strongly increased while also opening avenues for single cell profiling within heterogenous cell populations.

physics.optics

Non-obstructive intracellular nanolasers

Nanophotonic objects like plasmonic nanoparticles and colloidal quantum dots can complement the functionality of molecular dyes in biomedical optics. However, their operation is usually governed by spontaneous processes, which results in broad spectral features and limited signal-to-noise ratio, thus restricting opportunities for spectral multiplexing and sensing. Lasers provide the ultimate spectral definition and background suppression, and their integration with cells has recently been demonstrated. However, laser size and threshold remain problematic. Here, we report on the design, high-throughput fabrication and intracellular integration of semiconductor nanodisk lasers. By exploiting the large optical gain and high refractive index of GaInP/AlGaInP quantum wells, we obtain lasers with volumes 1000-fold smaller than the eukaryotic nucleus ($V_{laser}$<0.1 $μ$m$^3$), lasing thresholds 500-fold below the pulse energies typically used in two-photon microscopy ($E_{th} \approx $0.13 pJ), and excellent spectral stability (<50 pm wavelength shift). Multiplexed labelling with these lasers allows cells-tracking through micro-pores, thus providing a powerful tool to study cell migration and cancer invasion.

physics.optics

An exciton-polariton laser based on biologically produced fluorescent protein

Under adequate conditions, cavity-polaritons form a macroscopic coherent quantum state, known as Bose-Einstein condensate (BEC). Compared to Wannier-Mott excitons in inorganic semiconductors, the localized Frenkel excitons in organic emitter materials show weaker interaction but stronger coupling, which recently enabled the first realization of BEC at room temperature. However, this required ultrafast optical pumping which limits the applications of organic BECs. Here, we demonstrate room-temperature BEC of cavity-polaritons in simple laminated microcavities filled with the biologically produced enhanced green fluorescent protein (eGFP). The unique molecular structure of eGFP prevents exciton annihilation even at high excitation densities, thus facilitating BEC under conventional nanosecond pumping. BEC is clearly evidenced by a distinct threshold, an interaction-induced blueshift of the condensate, long-range coherence and the presence of a second threshold at higher excitation density which is associated with the onset of photon lasing and results from thermalization of the exciton reservoir.

cond-mat.mes-hall

Charge mobility determination by current extraction under linear increasing voltages: the case of non-equilibrium charges and field-dependent mobilities

The method of current extraction under linear increasing voltages (CELIV) allows for the simultaneous determination of charge mobilities and charge densities directly in thin films as used in organic photovoltaic cells (OPV). In the past, it has been specifically applied to investigate the interrelation of microstructure and charge transport properties in such systems. Numerical and analytical calculations presented in this work show that the evaluation of CELIV transients with the commonly used analysis scheme is error prone once charge recombination and, possibly, field dependent charge mobilities are taken into account. The most important effects are an apparent time-dependence of charge mobilities and errors in the determined field dependencies. Our results implicate that reports on time-dependent mobility relaxation in OPV materials obtained by the CELIV technique should be carefully revisited and confirmed by other measurement methods.

cond-mat.mtrl-sci