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Cambridge University Press eBooks

Surface coatings for atomic magnetometry

Scott J. Seltzer, Marie-Anne Bouchiat, M. V. Balabas

Published Mar 7, 2013• 6 citations
Publisher

Abstract

Introduction and history Paraffin films and other surface coatings have played a decisive role in the emergence and development of optical magnetometry. When alkali atoms in the vapor phase collide with the bare surface of a glass container, they disappear inside the glass and are replaced in the vapor phase by another atom with random spin orientation. With a mean free path of the dimensions of the cell (typically on the order of 1 to several cm), the collision frequency is much too high, 10 4 s −1 , to maintain the substantial spin polarization required for practical applications. In order to prevent this detrimental effect, vapor cells include either an inert buffer gas [1–3] or an antirelaxation surface coating [4]. In the presence of a noble gas at a pressure from 10 −2 to a few atmospheres, the alkali atoms diffuse very slowly from the center of the cell to the glass walls, and their orientation is only very slightly affected by gas collisions. However, there are several advantages to the use of a surface coating instead of buffer gas. If the static magnetic field is not homogeneous, then resonance lines suffer from inhomogeneous broadening in the presence of the gas [5–7]. In addition, the optical pumping process is perturbed by the buffer gas [8, 9]: (i) it is more efficient at the center of the cell than near the uncoated walls, so that the atomic orientation is inhomogeneous inside the cell; (ii) the pump beam absorption line is broadened, and its profile varies with the distance from the entrance window. These effects are unfavorable for the production of alignment in the ground state.

DOI
10.1017/cbo9780511846380.012

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Many technologies based on cells containing alkali-metal atomic vapor benefit from the use of antirelaxation surface coatings in order to preserve atomic spin polarization. In particular, paraffin has been used for this purpose for several decades and has been demonstrated to allow an atom to experience up to 10 000 collisions with the walls of its container without depolarizing, but the details of its operation remain poorly understood. We apply modern surface and bulk techniques to the study of paraffin coatings in order to characterize the properties that enable the effective preservation of alkali spin polarization. These methods include Fourier transform infrared spectroscopy, differential scanning calorimetry, atomic force microscopy, near-edge x-ray absorption fine structure spectroscopy, and x-ray photoelectron spectroscopy. We also compare the light-induced atomic desorption yields of several different paraffin materials. Experimental results include the determination that crystallinity of the coating material is unnecessary, and the detection of C[Double Bond]C double bonds present within a particular class of effective paraffin coatings. Further study should lead to the development of more robust paraffin antirelaxation coatings, as well as the design and synthesis of new classes of coating materials.

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The study of wall interactions of spin polarized rubidium atoms using the frequency shift in the electron paramagnetic resonance of the rubidium atoms

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I studied the effect of wall collisions on the electron paramagnetic resonance (EPR) of gas phase alkali metal atoms (87Rb). Two types of walls were studied: antirelaxation-coated walls and RbH-coated walls. I measured the dwell times of spin polarized Rb atoms on the two most common antirelaxation coatings, octadecyltrichlorosilane (OTS)- and paraffin. I found that at a cell temperature of 72 C the dwell times for OTS- and paraffin-coated walls are 0.9 ± 0.1 μs and 1.8 ± 0.2 μs, respectively. The implication of these dwell times, which are much longer than what was previously reported in the literature, is discussed in connection with the relaxing property of these coatings. In cells coated with RbH salt I made the first observation of the EPR frequency shift of the gas phase 87Rb atoms. Due to collisions with the RbH salt, which was nuclear spin polarized by spin exchange with optically pumped Rb vapor. The measured EPR frequency shifts are of the order of several hundred Hz in a millimeter-sized cell. By measuring the dependence of the EPR frequency shifts on cell length and by comparing the EPR frequency shifts in RbH-coated cells with those in OTS-coated cells, I provided convincing evidence that the observed EPR frequency shifts are due to collisions with RbH-coated walls, and not due to gas phase processes. The EPR frequency shift is due to the Fermi contact interaction between the s-electron of the adsorbed 87Rb atom and the polarized nucleus on the salt surface. The measured EPR frequency shifts allowed me to calculate the ensemble-averaged phase shift experienced by the Rb atom while adsorbed on the walls. Under our experimental condition this is about 70 mrad. My experiment opens up the possibility of studying surface NMR using gas phase EPR. The phase shift is proportional to the surface nuclear polarization, thus provides an interesting method for measuring the surface nuclear polarization using gas phase EPR. My observation will alert the high precision miniature atomic magnetometry community that collisions with cell walls may cause a systematic error and line broadening in the magnetic resonance frequency.

•Jan 1, 2014•0 citations
Introduction and history Paraffin films and other surface coatings have played a decisive role in the emergence and development of optical magnetometry. When alkali atoms in the vapor phase collide with the bare surface of a glass container, they disappear inside the glass and are replaced in the vapor phase by another atom with random spin orientation. With a mean free path of the dimensions of the cell (typically on the order of 1 to several cm), the collision frequency is much too high, 10 4 s −1 , to maintain the substantial spin polarization required for practical applications. In order to prevent this detrimental effect, vapor cells include either an inert buffer gas [1–3] or an antirelaxation surface coating [4]. In the presence of a noble gas at a pressure from 10 −2 to a few atmospheres, the alkali atoms diffuse very slowly from the center of the cell to the glass walls, and their orientation is only very slightly affected by gas collisions. However, there are several advantages to the use of a surface coating instead of buffer gas. If the static magnetic field is not homogeneous, then resonance lines suffer from inhomogeneous broadening in the presence of the gas [5–7]. In addition, the optical pumping process is perturbed by the buffer gas [8, 9]: (i) it is more efficient at the center of the cell than near the uncoated walls, so that the atomic orientation is inhomogeneous inside the cell; (ii) the pump beam absorption line is broadened, and its profile varies with the distance from the entrance window. These effects are unfavorable for the production of alignment in the ground state.
Many technologies based on cells containing alkali-metal atomic vapor benefit from the use of antirelaxation surface coatings in order to preserve atomic spin polarization. In particular, paraffin has been used for this purpose for several decades and has been demonstrated to allow an atom to experience up to 10 000 collisions with the walls of its container without depolarizing, but the details of its operation remain poorly understood. We apply modern surface and bulk techniques to the study of paraffin coatings in order to characterize the properties that enable the effective preservation of alkali spin polarization. These methods include Fourier transform infrared spectroscopy, differential scanning calorimetry, atomic force microscopy, near-edge x-ray absorption fine structure spectroscopy, and x-ray photoelectron spectroscopy. We also compare the light-induced atomic desorption yields of several different paraffin materials. Experimental results include the determination that crystallinity of the coating material is unnecessary, and the detection of C[Double Bond]C double bonds present within a particular class of effective paraffin coatings. Further study should lead to the development of more robust paraffin antirelaxation coatings, as well as the design and synthesis of new classes of coating materials.
The interaction of spin polarized cesium atoms on coated surfaces is examined. Coated surfaces find extensive applications in atomic devices-hydrogen masers and advanced rubidium frequency standards utilize wall coatings to obtain very narrow hyperfine resonances. A Cs atomic beam is hyperfine or spin polarized by optical pumping techniques using a single mode AlGaAs diode laser. The ground state distribution is probed before and after scattering from coated surfaces using laser induced fluorescence spectroscopy. The coatings under investigations are paraffin and organosilanes and these are known to be very weakly relaxing surfaces for polarized alkali atoms. The spin relaxation properties of paraffin and organosilane coatings have been studied in glass cell-vapor environment. In our experiments using polarized atomic beams, our goal is to examine in detail the hyperfine and spin relaxation properties of these coatings in a carefully controlled environment which is not possible in the gas cell environment. We measure the spin relaxation probability per wall collision as a function of temperature of the surface. Results of our studies will be presented.
Antirelaxation surface coatings allow long spin relaxation times in alkali-metal cells without buffer gas, enabling faster diffusion of the alkali atoms throughout the cell and giving larger signals due to narrower optical linewidths. Effective coatings were previously unavailable for operation at temperatures above 80 °C. We demonstrate that octadecyltrichlorosilane (OTS) can allow potassium or rubidium atoms to experience hundreds of collisions with the cell surface before depolarizing, and that an OTS coating remains effective up to about 170 °C for both potassium and rubidium. We consider the experimental concerns of operating without buffer gas and with minimal quenching gas at high vapor density, studying the stricter need for effective quenching of excited atoms and deriving the optical rotation signal shape for atoms with resolved hyperfine structure in the spin-temperature regime. As an example of a high-temperature application of antirelaxation coated alkali vapor cells, we operate a spin-exchange relaxation-free atomic magnetometer with sensitivity of 6 fT/Hz and magnetic linewidth as narrow as 2 Hz.
We measured the rate of velocity-changing collisions (VCCs) between alkali atoms and background gas in buffer-gas-free anti-spin-relaxation-coated cells. The average VCC rate in paraffin-coated rubidium vapor cells prepared in this work was 1×1061 \times 10^{6}1×106 s−1^{-1}−1, which corresponds to $\sim$1 mm in the mean free path of rubidium atoms. This short mean free path indicates that alkali atoms do not travel freely between the cell walls. In addition, we found that a heating process known as increases the VCC rate, and also confirmed that ripening improves the anti-relaxation performance of the coatings.
Abstract The spin polarization and spatial homogeneity of alkali metal atoms are critical characteristics that determine the performance of spin-exchange relaxation-free magnetometers. In buffer gas cells, these characteristics are influenced by optical broadening and alkali atomic motional restriction imposed by the buffer gas. In coated cells, the protective effect of the coating on atomic spins, combined with rapid atomic diffusion, leads to significantly superior spin polarization characteristics compared to those in high-pressure buffer gas cells. However, due to neglecting the influence of atom-coating interactions on atomic motion, the existing spin polarization and spatial distribution models fail to accurately describe the polarization characteristics in coated cells. In this paper, based on the Langevin–Bloch equation, a dynamic model considering interaction effects between alkali metal atoms and the coating as well as between the pump light and the hyperfine levels of alkali metal atoms is proposed to accurately describe the spin polarization and spatial distribution in coated cells. To validate the proposed model, a series of experiments were carried out. The results demonstrate that coated cells can maintain high spin polarization and spatial homogeneity even under conditions of low pump intensity and high temperature, which are in good agreement with the simulations. This work provides a theoretical reference for the design of high-performance and low-power quantum sensors.
I studied the effect of wall collisions on the electron paramagnetic resonance (EPR) of gas phase alkali metal atoms (87Rb). Two types of walls were studied: antirelaxation-coated walls and RbH-coated walls. I measured the dwell times of spin polarized Rb atoms on the two most common antirelaxation coatings, octadecyltrichlorosilane (OTS)- and paraffin. I found that at a cell temperature of 72 C the dwell times for OTS- and paraffin-coated walls are 0.9 ± 0.1 μs and 1.8 ± 0.2 μs, respectively. The implication of these dwell times, which are much longer than what was previously reported in the literature, is discussed in connection with the relaxing property of these coatings. In cells coated with RbH salt I made the first observation of the EPR frequency shift of the gas phase 87Rb atoms. Due to collisions with the RbH salt, which was nuclear spin polarized by spin exchange with optically pumped Rb vapor. The measured EPR frequency shifts are of the order of several hundred Hz in a millimeter-sized cell. By measuring the dependence of the EPR frequency shifts on cell length and by comparing the EPR frequency shifts in RbH-coated cells with those in OTS-coated cells, I provided convincing evidence that the observed EPR frequency shifts are due to collisions with RbH-coated walls, and not due to gas phase processes. The EPR frequency shift is due to the Fermi contact interaction between the s-electron of the adsorbed 87Rb atom and the polarized nucleus on the salt surface. The measured EPR frequency shifts allowed me to calculate the ensemble-averaged phase shift experienced by the Rb atom while adsorbed on the walls. Under our experimental condition this is about 70 mrad. My experiment opens up the possibility of studying surface NMR using gas phase EPR. The phase shift is proportional to the surface nuclear polarization, thus provides an interesting method for measuring the surface nuclear polarization using gas phase EPR. My observation will alert the high precision miniature atomic magnetometry community that collisions with cell walls may cause a systematic error and line broadening in the magnetic resonance frequency.