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Added by
Mohammadjavad Dowran
Publication date
2018
fields
Physics
and research's language is
English
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Quantum resources can enhance the sensitivity of a device beyond the classical shot noise limit and, as a result, revolutionize the field of metrology through the development of quantum-enhanced sensors. In particular, plasmonic sensors, which are widely used in biological and chemical sensing applications, offer a unique opportunity to bring such an enhancement to real-life devices. Here, we use bright entangled twin beams to enhance the sensitivity of a plasmonic sensor used to measure local changes in refractive index. We demonstrate a 56% quantum enhancement in the sensitivity of state-of-the-art plasmonic sensor with measured sensitivities on the order of $10^{-10}$RIU$/sqrt{textrm{Hz}}$, nearly 5 orders of magnitude better than previous proof-of-principle implementations of quantum-enhanced plasmonic sensors. These results promise significant enhancements in ultratrace label free plasmonic sensing and will find their way into areas ranging from biomedical applications to chemical detection.
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The measurement of parameters that describe kinetic processes is important in the study of molecular interactions. It enables a deeper understanding of the physical mechanisms underlying how different biological entities interact with each other, such as viruses with cells, vaccines with antibodies, or new drugs with specific diseases. In this work, we study theoretically the use of quantum sensing techniques for measuring the kinetic parameters of molecular interactions. The sensor we consider is a plasmonic resonance sensor -- a label-free photonic sensor that is one of the most widely used in research and industry. The first type of interaction we study is the antigen BSA interacting with antibody IgG1, which provides a large sensor response. The second type is the enzyme carbonic anhydrase interacting with the tumor growth inhibitor benzenesulfonamide, which produces a small sensor response. For both types of interaction we consider the use of two-mode Fock states, squeezed vacuum states and squeezed displaced states. We find that these quantum states offer an enhancement in the measurement precision of kinetic parameters when compared to that obtained with classical light. The results may help in the design of more precise quantum-based sensors for studying kinetics in the life sciences.
Kinetic models are essential for describing how molecules interact in a variety of biochemical processes. The estimation of a models kinetic parameters by experiment enables researchers to understand how pathogens, such as viruses, interact with other entities like antibodies and trial drugs. In this work, we report a proof-of-principle experiment that uses quantum sensing techniques to give a more precise estimation of kinetic parameters than is possible with a classical approach. The specific interaction we study is that of bovine serum albumin (BSA) binding to gold via an electrostatic mechanism. BSA is an important protein in biochemical research as it can be conjugated with other proteins and peptides to create sensors with a wide range of specificity. We use single photons generated via parametric down-conversion to probe the BSA-gold interaction in a plasmonic resonance sensor. We find that sub-shot-noise level fluctuations in the sensor signal allow us to achieve an improvement in the precision of up to 31.8% for the values of the kinetic parameters. This enhancement can in principle be further increased in the setup. Our work highlights the potential use of quantum states of light for sensing in biochemical research.
Photonic sensors have many applications in a range of physical settings, from measuring mechanical pressure in manufacturing to detecting protein concentration in biomedical samples. A variety of sensing approaches exist, and plasmonic systems in particular have received much attention due to their ability to confine light below the diffraction limit, greatly enhancing sensitivity. Recently, quantum techniques have been identified that can outperform classical sensing methods and achieve sensitivity below the so-called shot-noise limit. Despite this significant potential, the use of definite photon number states in lossy plasmonic systems for further improving sensing capabilities is not well studied. Here, we investigate the sensing performance of a plasmonic interferometer that simultaneously exploits the quantum nature of light and its electromagnetic field confinement. We show that, despite the presence of loss, specialised quantum resources can provide improved sensitivity and resolution beyond the shot-noise limit within a compact plasmonic device operating below the diffraction limit.
The recently discovered spin defects in hexagonal boron nitride (hBN), a layered van der Waals material, have great potential in quantum sensing. However, the photoluminescence and the contrast of the optically detected magnetic resonance (ODMR) of hBN spin defects are relatively low so far, which limits their sensitivity. Here we report a record-high ODMR contrast of 46$%$ at room temperature, and simultaneous enhancement of the photoluminescence of hBN spin defects by up to 17-fold by the surface plasmon of a gold-film microwave waveguide. Our results are obtained with shallow boron vacancy spin defects in hBN nanosheets created by low-energy He$^+$ ion implantation, and a gold-film microwave waveguide fabricated by photolithography. We also explore the effects of microwave and laser powers on the ODMR, and improve the sensitivity of hBN spin defects for magnetic field detection. Our results support the promising potential of hBN spin defects for nanoscale quantum sensing.
Present protocols of criticality enhanced sensing with open quantum sensors assume direct measurement of the sensor and omit the radiation quanta emitted to the environment, thereby omitting potentially valuable information. Here we propose a protocol for criticality enhanced sensing via continuous observation of the emitted radiation quanta. Under general assumptions, we establish a scaling theory for the global quantum Fisher information of the joint system and environment state at a dissipative critical point. We demonstrate that it obeys universal scaling laws featuring transient and long-time behavior governed by the underlying critical exponents. Importantly, such scaling laws exceed the standard quantum limit and can in principle satuarate the Heisenberg limit. To harness such advantageous scaling, we propose a practical sensing scheme based on continuous detection of the emitted quanta. In such a scheme a single interrogation corresponds to a (stochastic) quantum trajectory of the open system evolving under the non-unitary dynamics dependent on the parameter to be sensed and the back-action of the continuous measurement. Remarkably, we demonstrate that the associated precision scaling significantly exceeds that based on direct measurement of the critical steady state, thereby establishing the metrological value of detection of the emitted quanta at dissipative criticality. We illustrate our protocol via counting the photons emitted by the open Rabi model, a paradigmatic model for the study of dissipative phase transition with finite components. Our protocol is applicable to diverse open quantum sensors permitting continuous readout, and may find applications at the frontier of quantum sensing such as human-machine interface, magnetic diagnosis of heart disease and zero-field nuclear magnetic resonance.
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