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Optical and Quantum Sensing and Precision Metrology II

Quantum sensing and laser spectroscopy aided by plasmonic nanoantennas and nonclassical states of light

Alexei V. Sokolov, Zhi Yang Gao, Marlan O. Scully, Jizhou Wang, Zhenhuan Yi

Published Mar 19, 2025• 0 citations
Publisher
DOI
10.1117/12.3053200

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As is well known, light arising from Raman scattering on molecules shows nonclassical mutual correlations between the Stokes and anti-Stokes components. However, the practical use of nonclassical Raman light is limited, due to its low intensity. The Raman signal can be enhanced in surface-enhanced Raman scattering (SERS) experiments by placing Raman active molecules near a plasmonic nanoantenna, due to the Purcell effect. Since the main contribution to emission in SERS experiments is re-emitted light from the plasmonic nanoantenna with no nonclassical correlations, the question arises as to whether it is possible to simultaneously amplify the Raman signal and preserve the nonclassical correlations. In this work, we give a positive answer to this question. We show that plasmonic nanoantennas can be used to enhance the nonclassical light intensity. We demonstrate that the main factor causing deterioration of the cross correlations of SERS light is the fluorescent background of the plasmonic nanoantenna. We analyze the way in which the geometry of a plasmonic nanoantenna affects the nonclassical cross correlations of the Raman light, and show that there is an optimal size of plasmonic nanoantenna that both increases the Raman signal and preserves the nonclassical correlations of the light at the level of a single molecule. The obtained results pave the way for the creation of sources with controlled intensity and a degree of nonclassicality.
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.