SearcharxivSearch

arXiv subjects

Suichu Huang

Publications and source records attributed to Suichu Huang.

2 recordsLinked to original sources

Multimodal Guided Surface Lattice Resonances in Index-Discontinuous Environments

Surface lattice resonances (SLRs) in metasurfaces have become a transformative platform for subwavelength optical devices, leveraging their high quality (Q)-factors, pronounced local field enhancement, and extensive long-range interactions. However, current high-Q SLR implementations are fundamentally limited by their dependence on homogeneous dielectric environments. This restriction significantly hinders their applicability in emerging fields such as molecular sensing, where operation in heterogeneous dielectric media (e.g., interfaces with an aqueous or air cladding) is often indispensable. To overcome this limitation, we introduce guided surface lattice resonances (gSLRs) by integrating nanoparticle arrays within slab waveguides. This configuration facilitates efficient coupling between scattered light and Bloch modes, thereby enabling high-Q multimodal resonances even in index-discontinuous environments. Experimental validation under incoherent illumination demonstrates a Q-factor of 1489 in an index-mismatched surrounding. Furthermore, the coupling strength and resonance intensity of these multimodal gSLRs can be continuously modulated by adjusting the vertical displacement of the nanoparticle arrays within the slab layers. To augment the sensitivity to local dielectric variations, we investigate gSLRs in metasurfaces integrated with metallic substrates, demonstrating suitability for biomolecule detection. A mathematical sensing model, incorporating biochemical reaction kinetics and optical responses, is established by representing adsorbed molecules as a uniform dielectric layer and validated through bovine serum albumin (BSA) sensing experiments. This work not only advances the fundamental understanding of resonance engineering in complex media but also facilitates the development of ultrathin, ultra-compact nano-optical and optoelectronic devices.

physics.optics

Light-driven C-H bond activation mediated by 2D transition metal dichalcogenides

C-H bond activation enables the facile synthesis of new chemicals. While C-H activation in short-chain alkanes has been widely investigated, it remains largely unexplored for long-chain organic molecules. Here, we report light-driven C-H activation in complex organic materials mediated by 2D transition metal dichalcogenides (TMDCs) and the resultant solid-state synthesis of luminescent carbon dots in a spatially-resolved fashion. We unravel the efficient H adsorption and a lowered energy barrier of C-C coupling mediated by 2D TMDCs to promote C-H activation. Our results shed light on 2D materials for C-H activation in organic compounds for applications in organic chemistry, environmental remediation, and photonic materials.

cond-mat.mtrl-sci