464 research outputs found
Design and assembly considerations for Redox cells and stacks
Individual redox flow cells are arranged electrically in series and hydraulically in parallel to form a single assembly called a stack. The hardware currently being tested in the laboratory has an active electrode area of either 310 sq cm or 929 sq cm. Four 310 sq cm stacks, each consisting of 39 active cells, were incorporated into a 1.0 kW preprototype system. The physical design of the stack is very critical to the performance and efficiency of the redox storage sytem. This report will discuss the mechanical aspects of the cell and stack design for the current Redox hardware, with regard to sealing the stack internally as well as externally, minimizing shunt currents and minimizing the electrical resistance of the stack
An electrochemical rebalance cell for Redox systems
An electrochemical rebalance cell for maintaining electrochemical balance, at the system level, of the acidified aqueous iron chloride and chromium chloride reactant solutions in the redox energy storage system was constructed and evaluated. The electrochemical reaction for the cathode is Fe(+3) + e(-) yields Fe(+2), and that for the anode is 1/2H2 yields H(+) + e(-). The iron (carbon felt) electrode and the hydrogen (platinized carbon) electrode are separated by an anion exchange membrane. The performance of the rebalance cell is discussed as well as the assembly of a single rebalance cell and multicell stacks. Various cell configurations were tested and the results are presented and discussed. The rebalance cell was also used to demonstrate its ability, as a preparative tool, for making high purity solutions of soluble reduced metal ionic species. Preparations of titanium, copper, vanadium and chromium ions in acidified solutions were evaluated
Observation of a Large Atomic Parity Violation Effect in Ytterbium
Atomic parity violation has been observed in the 6s^2 1S0 - 5d6s 3D1 408-nm
forbidden transition of ytterbium. The parity-violating amplitude is found to
be two orders of magnitude larger than in cesium, where the most precise
experiments to date have been performed. This is in accordance with theoretical
predictions and constitutes the largest atomic parity-violating amplitude yet
observed. This also opens the way to future measurements of neutron skins and
anapole moments by comparing parity-violating amplitudes for various isotopes
and hyperfine components of the transition
Safety, the Preface Paradox and Possible Worlds Semantics
This paper contains an argument to the effect that possible worlds semantics renders
semantic knowledge impossible, no matter what ontological interpretation is given
to possible worlds. The essential contention made is that possible worlds semantic
knowledge is unsafe and this is shown by a parallel with the preface paradox
Isotopic variation of parity violation in atomic ytterbium
We report on measurements of atomic parity violation, made on a chain of
ytterbium isotopes with mass numbers A=170, 172, 174, and 176. In the
experiment, we optically excite the 6s2 1S0 -> 5d6s 3D1 transition in a region
of crossed electric and magnetic fields, and observe the interference between
the Stark- and weak-interaction-induced transition amplitudes, by making field
reversals that change the handedness of the coordinate system. This allows us
to determine the ratio of the weak-interaction-induced electric-dipole (E1)
transition moment and the Stark-induced E1 moment. Our measurements, which are
at the 0.5% level of accuracy for three of the four isotopes measured, allow a
definitive observation of the isotopic variation of the weak-interaction
effects in an atom, which is found to be consistent with the prediction of the
Standard Model. In addition, our measurements provide information about an
additional Z' boson.Comment: 19 pages, 4 figures, 2 table
Nonlinear magneto-optical rotation, Zeeman and hyperfine relaxation of potassium atoms in a paraffin-coated cell
Nonlinear magneto-optical Faraday rotation (NMOR) on the potassium D1 and D2 lines was used to study Zeeman relaxation rates in an antirelaxation paraffin-coated 3-cm diameter potassium vapor cell. Intrinsic Zeeman relaxation rates of were observed. The relatively small hyperfine intervals in potassium lead to significant differences in NMOR in potassium compared to rubidium and cesium. Using laser optical pumping, widths and frequency shifts were also determined for transitions between ground-state hyperfine sublevels of K atoms contained in the same paraffin-coated cell. The intrinsic hyperfine relaxation rate of Hz and a shift of Hz were observed. These results show that adiabatic relaxation gives only a small contribution to the overall hyperfine relaxation in the case of potassium, and the relaxation is dominated by other mechanisms similar to those observed in previous studies with rubidium
Observation of the 1S0 - 3P0 clock transition in 27Al+
We report for the first time, laser spectroscopy of the 1S0 - 3P0 clock
transition in 27Al+. A single aluminum ion and a single beryllium ion are
simultaneously confined in a linear Paul trap, coupled by their mutual Coulomb
repulsion. This coupling allows the beryllium ion to sympathetically cool the
aluminum ion, and also enables transfer of the aluminum's electronic state to
the beryllium's hyperfine state, which can be measured with high fidelity.
These techniques are applied to a measurement of the clock transition
frequency, \nu = 1 121 015 393 207 851(8) Hz. They are also used to measure the
lifetime of the metastable clock state, \tau = 20.6 +/- 1.4 s, the ground state
1S0 g-factor, g_S = -0.00079248(14), and the excited state 3P0 g-factor, g_P =
-0.00197686(21), in units of the Bohr magneton.Comment: 4 pages, 2 figures; updated author lis
Velocity-selective direct frequency-comb spectroscopy of atomic vapors
We present an experimental and theoretical investigation of two-photon direct
frequency-comb spectroscopy performed through velocity-selective excitation. In
particular, we explore the effect of repetition rate on the
two-photon transitions
excited in a rubidium atomic vapor cell. The transitions occur via step-wise
excitation through the states by use of the direct
output of an optical frequency comb. Experiments were performed with two
different frequency combs, one with a repetition rate of MHz and
one with a repetition rate of MHz. The experimental spectra are
compared to each other and to a theoretical model.Comment: 10 pages, 7 figure
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