arXiv subjects

Peter Zijlstra

Publications and source records attributed to Peter Zijlstra.

3 recordsLinked to original sources

arXiv2026

Suppressing Plasmonic Heating in Aqueous Environments with Hexagonal Boron Nitride

Optical heating of plasmonic nanostructures is a critical challenge in nanoscale systems. Although plasmonic effects enable enhanced optical functionalities, the associated temperature rise can degrade performance in heat-sensitive applications such as biosensing, nanophotonics, and microelectronics. Conventional cooling strategies fail at these scales due to limited heat transport and high interfacial thermal resistance, motivating the integration of advanced materials for thermal management. Here, we investigate hexagonal boron nitride (hBN) thin flakes as heat spreaders to mitigate plasmonic heating of gold nanospheres immobilized on hBN deposited on glass and surrounded by water. Using finite-element simulations, we quantify the influence of hBN thickness, in-plane thermal conductivity, and interfacial thermal conductance on cooling efficiency. Complementary experiments employ cross-grating wavefront microscopy (CGM) for nanothermometry to map the temperature around optically heated gold nanoparticles and quantify the cooling effect of hBN. We extend the application of CGM for rapid, non-invasive, and all-optical characterization of non-absorbing 2D materials. Our results reveal a strong thickness dependence, where heat dissipation in thin flakes is limited by the heat capacity of hBN and in thick flakes by interfacial thermal conductance. Including hBN, we obtain a reduction in temperature rise by up to 60% compared to glass. In addition, the presence of two main heat dissipation pathways emerges: a direct one from the nanoparticle to the hBN and an indirect one from the particle via water to the hBN. This combined simulation-experiment framework offers a versatile approach to improve thermal management in plasmonic systems and beyond, establishing design guidelines for integrating 2D materials into thermally sensitive platforms such as biosensors and integrated circuits.

physics.optics↗

arXiv2023

Exact particle-enhanced point-spread function unlocks 3D super-resolution localization microscopy on nanoparticles

Nanoparticles (NPs) have proven their applicability in biosensing, drug delivery, and photo-thermal therapy, but their performance depends critically on the distribution and number of functional groups on their surface. When studying surface functionalization using super-resolution microscopy, the NP modifies the fluorophores point-spread function (PSF). This leads to systematic mislocalizations in conventional analyses employing Gaussian PSFs. Here, we address this shortcoming by deriving the first-ever analytical PSF model for a fluorophore near a spherical NP. Its calculation is four orders of magnitude faster than numerical approaches and thus feasible for direct use in localization algorithms. We fit this model to individual 2D images from DNA-PAINT experiments on DNA-coated gold NPs and demonstrate extraction of the 3D positions of functional groups with <5 nm precision, revealing inhomogeneous surface coverage. Our method is exact, fast, accessible, and poised to become the standard in super-resolution imaging of NPs for biosensing and drug delivery applications.

physics.optics↗

arXiv2012

Optical detection of single non-absorbing molecules using the surface plasmon of a gold nanorod

Current optical detection schemes for single molecules require light absorption, either to produce fluorescence or direct absorption signals. This severely limits the range of molecules that can be detected, because most molecules are purely refractive. Metal nanoparticles or dielectric resonators detect non-absorbing molecules by a resonance shift in response to a local perturbation of the refractive index, but neither has reached single-protein sensitivity. The most sensitive plasmon sensors to date detect single molecules only when the plasmon shift is amplified by a highly polarizable label or by a localized precipitation reaction on the particle's surface. Without amplification, the sensitivity only allows for the statistical detection of single molecules. Here we demonstrate plasmonic detection of single molecules in realtime, without the need for labeling or amplification. We monitor the plasmon resonance of a single gold nanorod with a sensitive photothermal assay and achieve a ~ 700-fold increase in sensitivity compared to state-of-the-art plasmon sensors. We find that the sensitivity of the sensor is intrinsically limited due to spectral diffusion of the SPR. We believe this is the first optical technique that detects single molecules purely by their refractive index, without any need for photon absorption by the molecule. The small size, bio-compatibility and straightforward surface chemistry of gold nanorods may open the way to the selective and local detection of purely refractive proteins in live cells.

physics.chem-ph↗