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Reporters, Markers, Dyes, Nanoparticles, and Molecular Probes for Biomedical Applications

DNA-assembled plasmonic nanodiamonds: bright and stable single-photon emitters

Ishan Barman, Swati Tanwar

Published Mar 13, 2024• 0 citations
Publisher

Abstract

Unlocking the quantum potential of nitrogen-vacancy (NV) centers in diamonds has led to innovative advancements in sensing applications. By coupling NV centers with plasmonic nanostructures, ultrasensitive biolabels are envisioned. To this end, we exploit DNA self-assembly to create hybrid plasmonic nanodiamonds, featuring a closed nanocavity encapsulating a single nanodiamond. Correlated spectroscopy reveals enhanced brightness and emission rates, crucial for quantum sensing. This synergy between plasmonics and diamond fluorescence augments photon emission intensity and accelerates emission rates, enabling improved temporal resolution. These nanodiamonds hold promise as stable single-photon sources and versatile platforms for probing quantum effects in biology. This talk highlights the development, properties, and potential applications of these nanodiamonds, bridging quantum sensing and biomedicine, and fostering transformative changes in biophotonics.

DOI
10.1117/12.3008454

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Unlocking the quantum potential of nitrogen-vacancy (NV) centers in diamonds has led to innovative advancements in sensing applications. By coupling NV centers with plasmonic nanostructures, ultrasensitive biolabels are envisioned. To this end, we exploit DNA self-assembly to create hybrid plasmonic nanodiamonds, featuring a closed nanocavity encapsulating a single nanodiamond. Correlated spectroscopy reveals enhanced brightness and emission rates, crucial for quantum sensing. This synergy between plasmonics and diamond fluorescence augments photon emission intensity and accelerates emission rates, enabling improved temporal resolution. These nanodiamonds hold promise as stable single-photon sources and versatile platforms for probing quantum effects in biology. This talk highlights the development, properties, and potential applications of these nanodiamonds, bridging quantum sensing and biomedicine, and fostering transformative changes in biophotonics.
Fluorescent milled nanodiamonds are one of the most promising physical bases for quantum devices. The nitrogen vacancy (NV) center in diamond acts a room temperature, optically addressable quantum system which significantly decreases the infrastructure costs of developing quantum devices. Since nanodiamonds are nontoxic and colloidally stable, the nanoparticles are particularly attractive to the fields of sensing and nanomedicine where environmental changes must be detected with nanoscale resolution. Particle to particle irregularity, however, alters the spin and optical properties of each nanodiamond and complicates their integration into more complex systems. In this dissertation, we address the inhomogeneity of nanodiamonds and provide multiple paths towards fully utilizing these quantum emitters. First, we develop a technique for the self-assembly of nanodiamonds into arrays. We then utilize these arrays to perform a statistical study of the nanodiamonds and characterize the impact of the material’s surface and crystalline structure on the NV center’s optical and spin properties. Next, we establish a surface modification method that both improves the general properties of the nanodiamonds and enables chemical conjugation reactions. Together, these results deliver a newfound level of control and uniformity over an otherwise uncontrollable and polydisperse material.
The realization of scalable arrangements of nitrogen vacancy (NV) centers in diamond remains a key challenge on the way towards efficient quantum information processing, quantum simulation and quantum sensing applications. Although technologies based on implanting NV-centers in bulk diamond crystals or hybrid device approaches have been developed, they are limited by the achievable spatial resolution and by the intricate technological complexities involved in achieving scalability. We propose and demonstrate a novel approach for creating an arrangement of NV-centers, based on the self-assembling capabilities of biological systems and their beneficial nanometer spatial resolution. Here, a self-assembled protein structure serves as a structural scaffold for surface functionalized nanodiamonds, in this way allowing for the controlled creation of NV-structures on the nanoscale and providing a new avenue towards bridging the bio–nano interface. One-, two- as well as three-dimensional structures are within the scope of biological structural assembling techniques. We realized experimentally the formation of regular structures by interconnecting nanodiamonds using biological protein scaffolds. Based on the achievable NV-center distances of 11 nm, we evaluate the expected dipolar coupling interaction with neighboring NV-centers as well as the expected decoherence time. Moreover, by exploiting these couplings, we provide a detailed theoretical analysis on the viability of multiqubit quantum operations, suggest the possibility of individual addressing based on the random distribution of the NV intrinsic symmetry axes and address the challenges posed by decoherence and imperfect couplings. We then demonstrate in the last part that our scheme allows for the high-fidelity creation of entanglement, cluster states and quantum simulation applications.
Nitrogen-vacancy centers (NVs) are an atomic defect in diamond which possess remarkable fluorescence and spin properties which can be used for multiple metrological applications, particularly when the NV is hosted in nanodiamond, which can be easily integrated with a variety of nanoscale systems. A new class of nanodiamond hybrid nanostructures was developed using bottom-up synthesis methods. In this work, coupling between NV centers and plasmonic, excitonic and magnetic nanoparticles in these nanodiamond hybrid nanostructures is investigated using fluorescence lifetime measurements, spin relaxometry measurements and modeled using finite element method (FEM) and Monte Carlo simulations. This work not only characterizes the properties of these nanodiamond-hybrid nanostructures but also facilitates design guidelines for future hybrid structures with enhanced metrological and imaging capabilities.
Properties of quantum light represent a tool for overcoming limits of classical optics. Several experiments have demonstrated this advantage ranging from quantum enhanced imaging to quantum illumination. In this work, experimental demonstration of quantum-enhanced resolution in confocal fluorescence microscopy will be presented. This is achieved by exploiting the non-classical photon statistics of fluorescence emission of single nitrogen-vacancy (NV) color centers in diamond. By developing a general model of super-resolution based on the direct sampling of the kth-order autocorrelation function of the photoluminescence signal, we show the possibility to resolve, in principle, arbitrarily close emitting centers. Finally, possible applications of NV-based fluorescent nanodiamonds in biosensing and future developments will be presented.
Ultrafast emission rates obtained from quantum emitters coupled to plasmonic nanoantennas have recently opened fundamentally new possibilities in quantum information and sensing applications. Plasmonic nanoantennas greatly improve the brightness of quantum emitters by dramatically shortening their fluorescence lifetimes. Gap plasmonic nanocavities that support strongly confined modes are of particular interest for such applications. We demonstrate single-photon emission from nitrogen-vacancy (NV) centers in nanodiamonds coupled to nanosized gap plasmonic cavities with internal mode volumes about 10 000 times smaller than the cubic vacuum wavelength. The resulting structures features sub-nanosecond NV excited-state lifetimes and detected photon rates up to 50 million counts per second. Analysis of the fluorescence saturation allows the extraction of the multi-order excitation rate enhancement provided by the nanoantenna. Efficiency analysis shows that the NV center is producing up to 0.25 billion photons per second in the far-field.