Anchita Addhya | Searcharxiv

arXiv2025

Extending exciton and trion lifetimes in MoSe$_{2}$ with a nanoscale plasmonic cavity

Excitons in transition metal dichalcogenides (TMDs) have extremely short, picosecond-scale lifetimes which hinders exciton thermalization, limits the emergence of collective coherence, and reduces exciton transport in optoelectronic devices. In this work, we explore an all-optical pathway to extend exciton lifetimes by placing MoSe$_2$ in a deep-subwavelength Fabry-Perot silver cavity. The cavity structure is designed to suppress radiative recombination from in-plane optical dipoles, such as bright excitons and trions. We observe a consistent decrease in photoluminescence (PL) linewidths of excitons and trions (~1 nm), along with a corresponding lifetime increase (~10 ps). We confirm the experimental observations arise purely from exciton-cavity interactions-etching back the top silver layer returns the PL linewidth and lifetimes return to their original values. Our study offers a pathway to engineer excited state lifetimes in 2D materials which can be utilized for studies of optically dark excitons and have potential applications for novel optoelectronic devices.

cond-mat.mes-hall↗

arXiv2023

Direct-bonded diamond membranes for heterogeneous quantum and electronic technologies

Diamond has superlative material properties for a broad range of quantum and electronic technologies. However, heteroepitaxial growth of single crystal diamond remains limited, impeding integration and evolution of diamond-based technologies. Here, we directly bond single-crystal diamond membranes to a wide variety of materials including silicon, fused silica, sapphire, thermal oxide, and lithium niobate. Our bonding process combines customized membrane synthesis, transfer, and dry surface functionalization, allowing for minimal contamination while providing pathways for near unity yield and scalability. We generate bonded crystalline membranes with thickness as low as 10 nm, sub-nm interfacial regions, and nanometer-scale thickness variability over 200 by 200 $\mu m^2$ areas. We measure spin coherence times $T_2$ for nitrogen-vacancy centers in bonded membranes of up to 623(21) $\mu$s, suitable for advanced quantum applications. We demonstrate multiple methods for integrating high quality factor nanophotonic cavities with the diamond heterostructures, highlighting the platform versatility in quantum photonic applications. Furthermore, we show that our ultra-thin diamond membranes are compatible with total internal reflection fluorescence (TIRF) microscopy, which enables interfacing coherent diamond quantum sensors with living cells while rejecting unwanted background luminescence. The processes demonstrated herein provide a full toolkit to synthesize heterogeneous diamond-based hybrid systems for quantum and electronic technologies.

physics.app-ph↗