Spectroscopy of atomic spin noise allows the determination of many sample properties such as energy-level structures and transverse-spin relaxation rates without the need to drive the system away from equilibrium with applied fields. Analysis of noise measurements can also reveal the processes that limit the sensitivity of a measured signal. Standard methods for spectroscopic noise measurements in atomic vapors rely on far-off-resonant optical probing. We present a method for investigating spin noise with a probe beam frequency relatively close to resonance and show how the back action of the probe on the atomic state can be subtracted from the recorded noise spectra. We verify this method experimentally by showing noise data that scale with the square root of the number of atoms, after the probe back action has been properly subtracted.
Spectroscopy of atomic spin noise allows the determination of many sample properties such as energy-level structures and transverse-spin relaxation rates without the need to drive the system away from equilibrium with applied fields. Analysis of noise measurements can also reveal the processes that limit the sensitivity of a measured signal. Standard methods for spectroscopic noise measurements in atomic vapors rely on far-off-resonant optical probing. We present a method for investigating spin noise with a probe beam frequency relatively close to resonance and show how the back action of the probe on the atomic state can be subtracted from the recorded noise spectra. We verify this method experimentally by showing noise data that scale with the square root of the number of atoms, after the probe back action has been properly subtracted.
We explore the applications of spin noise spectroscopy (SNS) for detection of the spin properties of atomic ensembles in and out of equilibrium. In SNS, a linearly polarized far-detuned probe beam on passing through an ensemble of atomic spins acquires the information of the spin correlations of the system which is extracted using its time-resolved Faraday-rotation noise. We measure various atomic, magnetic and sub-atomic properties as well as perform precision magnetometry using SNS in rubidium atomic vapor in thermal equilibrium. Thereafter, we manipulate the relative spin populations between different ground state hyperfine levels of rubidium by controlled optical pumping which drives the system out of equilibrium. We then apply SNS to probe such spin imbalance non-perturbatively. We further use this driven atomic vapor to demonstrate that SNS can have better resolution than typical absorption spectroscopy in detecting spectral lines in the presence of various spectral broadening mechanisms.
We describe a relatively non-invasive optical spectroscopy technique, known as spin noise spectroscopy (SNS), to probe spontaneous magnetization fluctuations in an alkali atomic vapor at thermal equilibrium. The atomic magnetization at a non-zero temperature fluctuates about its equilibrium value, and such magnetization (spin) noise imparts fluctuation in the measured Faraday rotation of a far-detuned, linearly polarized probe laser beam passing through the vapor. This Faraday rotation fluctuation reveals the intrinsic spin dynamics of the electrons in the alkali vapor. We present a systematic experimental study of the SNS realized in thermal rubidium vapor and illustrate how one can measure various magnetic and chemical properties of the sample with minimal perturbation. We also demonstrate the applicability of this spectroscopy technique in measuring the spin populations and their dynamics in different hyperfine and magnetic levels by optically pumping the atomic system.
Spin noise sets fundamental limits to the attainable precision of measurements using spin-polarized atomic vapors and therefore merits a careful study. On the other hand, it has been recently shown that spin noise contains useful physical information about the atomic system, otherwise accessible via magnetic-resonance-type experiments. We here show in yet another manifestation of the fluctuation-dissipation theorem, that spin noise reveals information on the spin-coherence dissipation properties of the atomic system, described by 1∕T2, the transverse spin-relaxation rate. We present the high-resolution measurements of spin noise at a low magnetic field, leading to an accurate comparison of the extracted relaxation rates with the ones inferred from traditional magnetic-resonance-type measurements in optical pumping experiments.
Spin noise spectroscopy (SNS) allows optically detect the fluctuations of a spin ensemble. Such fluctuations induce noise in the birefringence of the medium, which can be probed by recording polarization fluctuations of a laser beam after its propagation through the sample. As spin fluctuations are centered on the zero frequency, a transverse magnetic field is applied: spin precession then shifts the spin noise resonance at the Larmor frequency, so that it is not hidden by technical noises. The first SNS experiment was reported in the early 1980s by Alexandrov and Zapasskii, but it is only in 2004 that advances in narrow linewidth lasers and low noise electronics allow using this technique to probe various systems, such as thermal atomic vapors, semiconductors, or quantum wells. It was also proposed for magnetic field sensing, and possible measurements of correlations beyond the second-order raise a lot of interest, as they can give access to new quantum phenomena. We have performed spin noise spectroscopy in a metastable helium gas cell, and show that we can get two polarization dependent noise peaks when we record the linear instead of the circular birefringence fluctuations. Moreover, the relatively simple structure of helium allows us to show that it depends on the closest optical transition even when we are detuned by more than the Doppler broadening. We can also show that the behavior of the polarization dependence is strongly affected by time dependent B-field fluctuations. We performed simulations using a density matrix time evolution model, with added random fluctuations. It reproduces quite well the experimental results, including the transition dependence and the time dependent B-field noise effect, which have not been reported yet.
Spin relaxometry using solid-state spin defects, such as the diamond nitrogen-vacancy (NV) center, probes dynamical processes by measuring how environmental fluctuations enhance the spin relaxation rate. In the weak-coupling limit, relaxation rates sample the transverse magnetic-noise power spectral density through a sensor-specific filter function, turning the defect into a local, frequency-selective noise spectrometer. This review bridges theory and experiment, clarifying how measured relaxation rates map onto noise spectra and how near-field geometry shapes the response. We highlight representative applications across condensed-matter physics, chemical and biological sensing, and relaxometry-based magnetic-resonance spectroscopy. We conclude with emerging opportunities and key challenges.
We study the fundamental limits of noise spectroscopy using estimation theory, Faraday rotation probing of an atomic spin system, and squeezed light. We find a simple and general expression for the Fisher information, which quantifies the sensitivity to spectral parameters such as resonance frequency and linewidth. For optically detected spin noise spectroscopy, we find that shot noise imposes ``local'' standard quantum limits for any given probe power and atom number, and also ``global'' standard quantum limits when the probe power and atom number are taken as free parameters. We confirm these estimation theory results using nondestructive Faraday rotation probing of hot Rb vapor, observing the predicted optima, and finding good quantitative agreement with a first-principles calculation of the spin noise spectra. Finally, we show sensitivity beyond the atom- and photon-number-optimized global standard quantum limit using squeezed light.