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arXiv:1512.07511 · Journal of Physics B Atomic Molecular and Optical Physics

Adsorbate dynamics on a silica-coated gold surface measured by Rydberg Stark spectroscopy

Julian B. Naber, Shimon Machluf, Lara Torralbo-Campo, Maarten L. Soudijn, N. J. van Druten, H. B. van Linden van den Heuvell, R. J. C. Spreeuw

Published Apr 20, 2016• 16 citations
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Abstract

Trapping a Rydberg atom close to a surface is an important step towards the realisation of many proposals for quantum information processing or hybrid quantum systems. One of the challenges in these experiments is posed by the electric field emanating from contaminations on the surface. Here we report on measurements of an electric field created by 87 Rb atoms adsorbed on a 25 nm thick layer of SiO 2 , covering a 90 nm layer of Au. The electric field is measured using a two-photon transition to the and states. The electric field value that we measure is higher than typical values measured above metal surfaces, but is consistent with a recent measurement above a SiO 2 surface. In addition, we measure the temporal behaviour of the field and observe that we can reduce it in a single experimental cycle, using ultraviolet light or by mildly locally heating the surface with one of the excitation lasers, whereas the buildup of the field takes thousands of cycles. We explain these results by a change in the adatom distribution on the surface. These results indicate that, while the stray electric field can be reduced, achieving field-free conditions above a silica-coated gold chip remains challenging.

DOI
10.1088/0953-4075/49/9/094005

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Trapping a Rydberg atom close to a surface is an important step towards the realisation of many proposals for quantum information processing or hybrid quantum systems. One of the challenges in these experiments is posed by the electric field emanating from contaminations on the surface. Here we report on measurements of an electric field created by 87 Rb atoms adsorbed on a 25 nm thick layer of SiO 2 , covering a 90 nm layer of Au. The electric field is measured using a two-photon transition to the and states. The electric field value that we measure is higher than typical values measured above metal surfaces, but is consistent with a recent measurement above a SiO 2 surface. In addition, we measure the temporal behaviour of the field and observe that we can reduce it in a single experimental cycle, using ultraviolet light or by mildly locally heating the surface with one of the excitation lasers, whereas the buildup of the field takes thousands of cycles. We explain these results by a change in the adatom distribution on the surface. These results indicate that, while the stray electric field can be reduced, achieving field-free conditions above a silica-coated gold chip remains challenging.
Experiments handling Rydberg atoms near surfaces must necessarily deal with the high sensitivity of Rydberg atoms to (stray) electric fields that typically emanate from adsorbates on the surface. We demonstrate a method to modify and reduce the stray electric field by changing the adsorbate distribution. We use one of the Rydberg excitation lasers to locally affect the adsorbed dipole distribution. By adjusting the averaged exposure time we change the strength (with the minimal value less than 0.2V/cm0.2\phantom{\rule{0.28em}{0ex}}\mathrm{V}/\mathrm{cm}0.2V/cm at $78\phantom{\rule{0.28em}{0ex}}\ensuremath{\mu}\mathrm{m}$ from the chip) and even the sign of the perpendicular field component. This technique is a useful tool for experiments handling Rydberg atoms near surfaces, including atom chips.
We demonstrate spatially resolved, coherent excitation of Rydberg atoms on an atom chip. Electromagnetically induced transparency (EIT) is used to investigate the properties of the Rydberg atoms near the gold-coated chip surface. We measure distance-dependent shifts ( ~ 101010 MHz) of the Rydberg energy levels caused by a spatially inhomogeneous electric field. The measured field strength and distance dependence is in agreement with a simple model for the electric field produced by a localized patch of Rb adsorbates deposited on the chip surface during experiments. The EIT resonances remain narrow (<4<4<4 MHz) and the observed widths are independent of atom-surface distance down to  ~ 202020 $\ensuremath{\mu}$m, indicating relatively long lifetime of the Rydberg states. Our results open the way to studies of dipolar physics, collective excitations, quantum metrology, and quantum information processing involving interacting Rydberg excited atoms on atom chips.
We have investigated Rb adsorbates on the SiO 2 (0001) surface. Using Rydberg atom electromagnetically induced transparency, we investigate the electric fields resulting from Rb adsorbed on the quartz surface, and measure the activation energy of the Rb adsorbates. We show that the adsorbed Rb induces a negative electron affinity (NEA) on the quartz surface. The NEA surface allows low energy electrons to bind to the surface and cancel the electric field from the Rb adsorbates. Our results are important for integrating Rydberg atoms into hybrid quantum systems and the fundamental study of atom-surface interactions, as well as applications for electrons bound to a surface.
On one side, atom-chip experiments have demonstrated to be a versatile tool to study quantum physics in cold atoms systems. On the other side, Rydberg atoms have exaggerated properties that makes them good candidates to study quantum information and quantum simulations protocols. In this thesis both system are put together with the aim to study Rydberg physics (in particular atom-atom interaction) in an atom-chip experiment. Due to the exaggerated properties of Rydberg atoms they are very sensitive to electric fields. Thus, the combination of Rydberg atoms with surfaces can be challenging. Therefore a detailed characterization of the mentioned stray electric fields via the analysis of Stark-Zeeman maps is crucial. We employ two-photon Rydberg Stark spectroscopy of a micron-sized cloud of magnetically trapped ultracold rubidium atoms to characterize the electric fields near our atom-chip. Once we characterized the local electric fields we were able to study in more detail the effect of Rydberg excitation in the ultracold cloud of atoms. For instance we observed the formation of ultralong-range Rydberg molecules in our system. In these molecules a ground state atom is weakly bound to the Rydberg electron. We also attempted to observe the effect of Rydberg blockade in the system by looking at the characteristics of Rydberg spectra. Finally we studied the possibility of inducing rf transitions within a Rydberg state manifold in order to enhance our detection method and populate states that are not accessible directly with a two-photon laser transition.
We investigate the behavior of electric fields originating from adsorbates deposited on a cryogenic atom chip as it is cooled from room temperature to cryogenic temperature. Using Rydberg electromagnetically induced transparency, we measure the field strength versus distance from a 1 mm square of yttrium barium copper oxide (YBCO) patterned onto a yttria stabilized zirconia chip substrate. We find a localized and stable dipole field at room temperature and attribute it to a saturated layer of chemically adsorbed rubidium atoms on the YBCO. As the chip is cooled towards 83 K we observe a change in sign of the electric field as well as a transition from a localized to a delocalized dipole density. We relate these changes to the onset of physisorption on the chip surface when the van der Waals attraction overcomes the thermal desorption mechanisms. Our findings suggest that through careful selection of substrate materials, it may be possible to reduce the electric fields caused by atomic adsorption on chips, opening up experiments to controlled Rydberg-surface coupling schemes.
Hybrid quantum platforms based on highly excited Rydberg atoms coupled to nanophotonics devices offer a promising route toward scalable quantum networks and integrated quantum technologies. However, the close proximity of Rydberg atoms to dielectric nanostructures makes these systems particularly susceptible to uncontrolled surface electric fields that can lead to a degradation of the excitation process. Here, we experimentally investigate Rydberg excitation of laser-cooled 87^{87}87Rb atoms via the evanescent field of an optical nanofiber in the presence of fiber-guided red- and blue-detuned light fields as used to trap ground state atoms in fiber-based dipole traps. We observe a time evolution of the Rydberg excitation spectrum when both the dipole trapping fields are on and the additional spectral features that appear can be suppressed by applying an external oscillating electric field to the system, strongly indicating that surface charge accumulation is responsible for the observed spectral feature. The experimental results are reproduced qualitatively by a model that incorporates DC energy level shifts arising from electric fields generated by charges deposited on the nanofiber surface. We identify Rydberg-ground state collisional ionization, which is enhanced by the dipole trapping fields, as the dominant mechanism for charge generation. These results provide new insight into charge dynamics at dielectric nanophotonic interfaces and establish practical guidelines for mitigating surface charge-induced electric fields in fiber-integrated Rydberg quantum systems.