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arXiv:2003.06970

Quantum Sensing by Using STIRAP with Dressed States Driving

Hao Zhang, Guo‐Qing Qin, Xue‐Ke Song, Gui‐Lu Long

Published Mar 16, 2020• 0 citations
arXivHTMLPDF

Abstract

Exploring quantum technology to precisely measure physical quantities is a meaningful task for practical scientific researches. Here, we propose a novel quantum sensing model based on dressed states driving (DSD) in stimulated Raman adiabatic passage. The model is universal for sensing different physical quantities, such as magnetic field, mass, rotation and etc. For different sensors, the used systems can range from macroscopic scale, e.g. optomechanical systems, to microscopic nanoscale, e.g. nitrogen-vacancy color centres in diamond. By investigating the dynamics of color detuning of DSD passage, the results show the sensitivity of sensors can be enhanced by tuning system with more adiabatic and accelerated processes in non-degenerate and degenerate color detuning regime, respectively. To show application examples, we apply our approach to build optomechanical mass sensor and solid spin magnetometer with practical parameters.

DOI
10.48550/arxiv.2003.06970

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Exploring quantum technology to precisely measure physical quantities is a meaningful task for practical scientific researches. Here, we propose a novel quantum sensing model based on dressed states driving (DSD) in stimulated Raman adiabatic passage. The model is universal for sensing different physical quantities, such as magnetic field, mass, rotation and etc. For different sensors, the used systems can range from macroscopic scale, e.g. optomechanical systems, to microscopic nanoscale, e.g. nitrogen-vacancy color centres in diamond. By investigating the dynamics of color detuning of DSD passage, the results show the sensitivity of sensors can be enhanced by tuning system with more adiabatic and accelerated processes in non-degenerate and degenerate color detuning regime, respectively. To show application examples, we apply our approach to build optomechanical mass sensor and solid spin magnetometer with practical parameters.
Exploring quantum technology to precisely measure physical quantities is a meaningful task for practical scientific researches. Here, we propose a novel quantum sensing model based on color detuning dynamics with dressed states driving (DSD) in stimulated Raman adiabatic passage. The model is valid for sensing different physical quantities, such as magnetic field, mass, rotation and so on. For different sensors, the used systems can range from macroscopic scale, e.g. optomechanical systems, to microscopic nanoscale, e.g. solid spin systems. The dynamics of color detuning of DSD passage indicates the sensitivity of sensors can be enhanced by tuning system with more adiabatic or accelerated processes in different color detuning regimes. To show application examples, we apply our approach to build optomechanical mass sensor and solid spin magnetometer with practical parameters.
We report the first experimental demonstration of stimulated Raman adiabatic passage (STIRAP) in nuclear-spin transitions of 14^{14}14N within nitrogen-vacancy (NV) color centers in diamond. It is shown that the STIRAP technique suppresses the occupation of the intermediate state, which is a crucial factor for improvements in quantum sensing technology. Building on that advantage, we develop and implement a generalized version of the Ramsey interferometric scheme, employing half-STIRAP pulses to perform the necessary quantum-state manipulation with high fidelity. The enhanced robustness of the STIRAP-based Ramsey scheme to variations in the pulse parameters is experimentally demonstrated, showing good agreement with theoretical predictions. Our results pave the way for improving the long-term stability of diamond-based sensors, such as gyroscopes and frequency standards.
Abstract Stimulated Raman adiabatic passage (STIRAP) is a widely used technique for efficient population transfer between quantum states. However, the adiabatic nature of STIRAP requires slow evolution, leading to long operation times, which limits its practical applications. The superadiabatic method has been introduced to accelerate the STIRAP process, but it often necessitates additional couplings between the initial and target states, which may not be available in the original Hamiltonian. In this work, we present a novel approach to implement superadiabatic STIRAP (sa-STIRAP) between dressed states in a three-level quantum system. By modulating the amplitude and phase of the original driving fields, the initial and target states in dressed-state space can be effectively coupled. This approach provides a practical means of realizing sa-STIRAP in experimental setups, making it convenient to accelerate adiabatic quantum state transfer.
Abstract We report the first experimental demonstration of stimulated Raman adiabatic passage (STIRAP) in nuclear-spin transitions of 14N within nitrogen-vacancy color centers in diamond. It is shown that the STIRAP technique suppresses the occupation of the intermediate state, which is a crucial factor for improvements in quantum sensing technology. Building on that advantage, we develop and implement a generalized version of the Ramsey interferometric scheme, employing half-STIRAP pulses to perform the necessary quantum-state manipulation with high fidelity. The enhanced robustness of the STIRAP-based Ramsey scheme to variations in the pulse parameters is experimentally demonstrated, showing good agreement with theoretical predictions. Our results pave the way for improving the long-term stability of diamond-based sensors, such as gyroscopes and frequency standards.
Versatile nanoscale sensors that are susceptible to changes in a variety of physical quantities often exhibit limited selectivity. We propose a novel scheme based on microwave-dressed spin states for optically probed nanoscale temperature detection using diamond quantum sensors, which provides selective sensitivity to temperature changes. By combining this scheme with a continuous pump-probe scheme using ensemble nitrogen-vacancy centers in nanodiamonds, we demonstrate a sub-100-nanosecond temporal resolution with thermal sensitivity of 3.7 K⋅\cdot⋅Hz−1/2^{-1/2}−1/2 that is insensitive to variations in external magnetic fields on the order of 2 G. The presented results are favorable for the practical application of time-resolved nanoscale quantum sensing, where temperature imaging is required under fluctuating magnetic fields.
Solid-state spin ensembles have emerged as a leading platform for micro- and nanoscale sensing, combining high sensitivity, nanoscale spatial resolution, and operation under ambient conditions. At high spin densities, magnetic dipole–dipole interactions typically limit sensing performance by reducing coherence, but can in principle be harnessed to enhance sensitivity. Realizing such interaction-enhanced sensing in practice, however, remains challenging due to the intrinsic anisotropy of dipolar interactions and the random spatial distribution of spins. This thesis presents a series of experimental works that culminate in a practical interaction-enhanced magnetometer based on ensembles of nitrogen-vacancy (NV) centers in diamond. Our approach is based on collective, one-axis-twisting-like (OAT-like) dynamics engineered from native dipolar interactions using controlled nanoscale spin textures, in combination with a dressed-state qubit encoding that significantly extends the sensor coherence time. These results open the door to practical deployment of interaction-enhanced quantum sensors for nanoscale biological imaging and material characterization.