Enhanced nuclear spin dependent parity violation effects using the 199HgH molecule

Electron interactions with the nuclear-spin-dependent (NSD) parity non-conserving (PNC) anapole moment are strongly enhanced within heteronuclear diatomic molecules. A novel, low-energy optical rotation experiment is being proposed with the aim of observing NSD PNC interactions in HgH. Based on the relativistic coupled cluster method we present a complete calculation of the circular polarization parameter $P = 2\,\textrm{Im}(E1_{PNC})/M1 \approx 3 \times 10^{-6}\; \kappa$ for the $^2\Sigma_{1/2} \to ^2\Pi_{1/2}$ optical transition of HgH, where $\kappa$ is a dimensionless constant determined by the nuclear anapole moment. This provides an improvement in sensitivity to NSD PNC by 2 -- 3 orders of magnitude over the leading atomic Xe, Hg, Tl, Pb and Bi optical rotation experiments, and shows that the proposed measurement will be sensitive enough to extract the $^{199}$Hg anapole moment and shed light on the underlying theory of hadronic parity violation

Stark shift and parity non-conservation for near-degenerate states of xenon

We identify a pair of near-degenerate states of opposite parity in atomic Xe, the 5p^5 10s \,\, ^2[3/2]_2^o at $\rm{E}=94759.927$ cm$^{-1}$ and 5p^5 6f \,\, ^2[5/2]_2 at $\rm{E}= 94759.935$ cm$^{-1}$, for which parity- and time-odd effects are expected to be enhanced by the small energy separation. We present theoretical calculations which indicate narrow widths for both states and we report a calculated value for the weak matrix element, arising from configuration mixing, of $|W|=2.1$ Hz for $^{132}$Xe. In addition, we measured the Stark effect of the $5p^5\,6f$ $^2[5/2]_{2}$ and $5p^5 \,6f \ ^2[3/2]_2$ ($\rm{E} =94737.121\,\rm{cm}^{-1}$) states. The Stark-shift of the $6f$ states is observed to be negative, revealing the presence of nearby $6g$ states at higher energies, which have not been observed before. The Stark-shift measurements imply an upper limit on the weak matrix element of $|W|\!<\!5$ Hz for the near-degenerate states (10s \,\, ^2[3/2]_2^o and 6f \,\, ^2[5/2]_2), which is in agreement with the presented calculations.Comment: 11 pages, 6 figure

Absolute absorption cross-section measurements of CO2 in the ultraviolet from 200 to 206 nm at 295 and 373 K

Laboratory measurements of the absolute absorption cross-section of CO 2 at the temperatures 295 and 373 K have been made between 200 and 206 nm using cavity ring-down spectroscopy. Below 205 nm, the cross-section at 373 K is significantly larger than at 295 K, whereas beyond 205 nm measurements at both temperatures yield cross-sections approximately equal to the Rayleigh scattering cross-section, within experimental error. The present measurements should resolve a long-standing discrepancy between previously published data on this system. © 2004 Elsevier B.V. All rights reserved