95 research outputs found
Zeeman-resolved Autler-Townes splitting in Rydberg atoms with tunable resonances and a single transition dipole moment
Applying a magnetic field as a method for tuning the frequency of
Autler-Townes splitting for Rydberg electrometry has recently been
demonstrated. In this paper we provide a theoretical understanding of EIT
signals in the presence of a large magnetic field, as well as demonstrate some
advantages of this technique over traditional Autler-Townes based electrometry.
We show that a strong magnetic field provides a well-defined quantization axis
regardless of the optical field polarizations, we demonstrate that by
separating the levels of the Rydberg state we can perform an
Autler-Townes splitting with a single participating dipole moment, and we
demonstrate recovery of signal strength by populating a single level
using circularly polarized light
Phase-Resolved Rydberg Atom Field Sensing using Quantum Interferometry
Although Rydberg atom-based electric field sensing provides key advantages
over traditional antenna-based detection, it remains limited by the need for a
local oscillator (LO) for low-field and phase resolved detection. In this work,
we demonstrate that closed-loop quantum interferometric schemes can be used to
generate a system-internal reference that can directly replace an external LO
for Rydberg field sensing. We reveal that this quantum-interferometrically
defined internal reference phase and frequency can be used analogously to a
traditional LO for atom-based down-mixing to an intermediate frequency for
lock-in phase detection. We demonstrate that this LO-equivalent functionality
provides analogous benefits to an LO, including full 360 phase
resolution as well as improved sensitivity. The general applicability of this
approach is confirmed by demodulating a four phase-state signal broadcast on
the atoms. Our approach opens up new sensing schemes and provides a clear path
towards all-optical Rydberg atom sensing implementations
Sensitivity Comparison of Two-photon vs Three-photon Rydberg Electrometry
We investigate the sensitivity of three-photon EIT in Rydberg atoms to radio
frequency detection and compare it against conventional two-photon systems.
Specifically, we model the 4-level and 5-level atomic system and compare how
the transmission of the probe changes with different powers of the lasers used
and strengths of the RF field. In this model, we also define a sensitivity
metric to best relate to the operation of the current best experimental
implementation based on shot noise limited detection. We find that the
three-photon system boasts much narrower line widths compared to the
conventional two-photon EIT. However, these narrow line features do not align
with the regions of the best sensitivity. In addition to this, we calculate the
expected sensitivity for the two-photon Rydberg sensor and find that the best
achievable sensitivity is over an order of magnitude better than the current
measured values of 5 uV/m/Hz. However, by accounting for the additional noise
sources in the experiment and the quantum efficiency of the photo-detectors,
the values are in good agreement.Comment: 9 pages, 6 figure
Independent Rydberg Atom Sensing using a Dual-Ladder Scheme
Rydberg atom-based electric field sensing can provide all-optical readout of
radio frequency fields in a dielectric environment. However, because a single
set of optical fields is typically used to prepare the Rydberg state and read
out its response to RF fields, it is challenging to perform simultaneous and
independent measurements of the RF field(s). Here we show that using two
independent schemes to prepare and read out the same Rydberg state can be used
to perform independent measurements in general, which we demonstrate
specifically by resolving the the RF polarization. We expect this work will be
useful for fiber-coupled sensor heads where spatial multiplexing is
challenging, as well as for complex multi-level sensing schemes
Detection of HF and VHF Fields through Floquet Sideband Gaps by `Rabi Matching' Dressed Rydberg Atoms
Radio frequencies in the HF and VHF (3 MHz to 300 MHz) bands are challenging
for Rydberg atom-based detection schemes, as resonant detection requires
exciting the atoms to extremely high energy states. We demonstrate a method for
detecting and measuring radio frequency (RF) carriers in the HF and VHF bands
via a controlled Autler-Townes line splitting. Using a resonant, high-frequency
(GHz) RF field, the absorption signal from Townes-Merrit sidebands created by a
low frequency, non-resonant RF field can be enhanced. Notably, this technique
uses a measurement of the optical frequency separation of an avoided crossing
to determine the amplitude of a non-resonant, low frequency RF field. This
technique also provides frequency-selective measurements of low frequency RF
electric fields. To show this, we demonstrate amplitude modulated signal
transduction on a low frequency VHF carrier. We further demonstrate reception
of multiple tones simultaneously, creating a Rydberg `spectrum analyzer' over
the VHF range.Comment: Data for figures can be found at:
https://datapub.nist.gov/od/id/mds2-285
Increased instantaneous bandwidth of Rydberg atom electrometry with an optical frequency comb probe
We show that the use of an optical frequency comb probe leads to dramatically
improved bandwidth (as high as 12+/-1 MHz) for the detection of modulated radio
frequencies in Rydberg atom-based electrometry
Ultrafast nano-focusing with full optical waveform control
The spatial confinement and temporal control of an optical excitation on
nanometer length scales and femtosecond time scales has been a long-standing
challenge in optics. It would provide spectroscopic access to the elementary
optical excitations in matter on their natural length and time scales and
enable applications from ultrafast nano-opto-electronics to single molecule
quantum coherent control. Previous approaches have largely focused on using
surface plasmon polariton (SPP) resonant nanostructures or SPP waveguides to
generate nanometer localized excitations. However, these implementations
generally suffer from mode mismatch between the far-field propagating light and
the near-field confinement. In addition, the spatial localization in itself may
depend on the spectral phase and amplitude of the driving laser pulse thus
limiting the degrees of freedom available to independently control the
nano-optical waveform. Here we utilize femtosecond broadband SPP coupling, by
laterally chirped fan gratings, onto the shaft of a monolithic noble metal tip,
leading to adiabatic SPP compression and localization at the tip apex. In
combination with spectral pulse shaping with feedback on the intrinsic
nonlinear response of the tip apex, we demonstrate the continuous micro- to
nano-scale self-similar mode matched transformation of the propagating
femtosecond SPP field into a 20 nm spatially and 16 fs temporally confined
light pulse at the tip apex. Furthermore, with the essentially wavelength and
phase independent 3D focusing mechanism we show the generation of arbitrary
optical waveforms nanofocused at the tip. This unique femtosecond nano-torch
with high nano-scale power delivery in free space and full spectral and
temporal control opens the door for the extension of the powerful nonlinear and
ultrafast vibrational and electronic spectroscopies to the nanoscale.Comment: Contains manuscript with 4 figures as well as supplementary material
with 2 figure
A Hydrophobic Gate in an Ion Channel: The Closed State of the Nicotinic Acetylcholine Receptor
The nicotinic acetylcholine receptor (nAChR) is the prototypic member of the
`Cys-loop' superfamily of ligand-gated ion channels which mediate synaptic
neurotransmission, and whose other members include receptors for glycine,
gamma-aminobutyric acid, and serotonin. Cryo-electron microscopy has yielded a
three dimensional structure of the nAChR in its closed state. However, the
exact nature and location of the channel gate remains uncertain. Although the
transmembrane pore is constricted close to its center, it is not completely
occluded. Rather, the pore has a central hydrophobic zone of radius about 3 A.
Model calculations suggest that such a constriction may form a hydrophobic
gate, preventing movement of ions through a channel. We present a detailed and
quantitative simulation study of the hydrophobic gating model of the nicotinic
receptor, in order to fully evaluate this hypothesis. We demonstrate that the
hydrophobic constriction of the nAChR pore indeed forms a closed gate.
Potential of mean force (PMF) calculations reveal that the constriction
presents a barrier of height ca. 10 kT to the permeation of sodium ions,
placing an upper bound on the closed channel conductance of 0.3 pS. Thus, a 3 A
radius hydrophobic pore can form a functional barrier to the permeation of a 1
A radius Na+ ion. Using a united atom force field for the protein instead of an
all atom one retains the qualitative features but results in differing
conductances, showing that the PMF is sensitive to the detailed molecular
interactions.Comment: Accepted by Physical Biology; includes a supplement and a
supplementary mpeg movie can be found at
http://sbcb.bioch.ox.ac.uk/oliver/download/Movies/watergate.mp
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