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1. High-dimensional discrete Fourier transform gates with a quantum frequency processor

   https://doi.org/10.1364/OE.454677  

   Lu, Hsuan-Hao; Lingaraju, Navin_B; Leaird, Daniel_E; Weiner, Andrew_M; Lukens, Joseph_M (March 2022, Optics Express)

   The discrete Fourier transform (DFT) is of fundamental interest in photonic quantum information, yet the ability to scale it to high dimensions depends heavily on the physical encoding, with practical recipes lacking in emerging platforms such as frequency bins. In this article, we show thatd-point frequency-bin DFTs can be realized with a fixed three-component quantum frequency processor (QFP), simply by adding to the electro-optic modulation signals one radio-frequency harmonic per each incremental increase ind. We verify gate fidelity ${\mathcal{F}}_W>0.9997$and success probability ${\mathcal{P}}_W>0.965$up tod = 10 in numerical simulations, and experimentally implement the solution ford = 3, utilizing measurements with parallel DFTs to quantify entanglement and perform tomography of multiple two-photon frequency-bin states. Our results furnish new opportunities for high-dimensional frequency-bin protocols in quantum communications and networking. 

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2. Spectrally simplified approach for leveraging legacy geostationary oceanic observations

   https://doi.org/10.1364/AO.465491  

   Houskeeper, Henry_F; Hooker, Stanford_B; Cavanaugh, Kyle_C (September 2022, Applied Optics)

   The use of multispectral geostationary satellites to study aquatic ecosystems improves the temporal frequency of observations and mitigates cloud obstruction, but no operational capability presently exists for the coastal and inland waters of the United States. The Advanced Baseline Imager (ABI) on the current iteration of the Geostationary Operational Environmental Satellites, termed the $R$Series (GOES-R), however, provides sub-hourly imagery and the opportunity to overcome this deficit and to leverage a large repository of existing GOES-R aquatic observations. The fulfillment of this opportunity is assessed herein using a spectrally simplified, two-channel aquatic algorithm consistent with ABI wave bands to estimate the diffuse attenuation coefficient for photosynthetically available radiation, $K_d\left(\mathrm{P}\mathrm{A}\mathrm{R}\right)$. First, anin situABI dataset was synthesized using a globally representative dataset of above- and in-water radiometric data products. Values of $K_d\left(\mathrm{P}\mathrm{A}\mathrm{R}\right)$were estimated by fitting the ratio of the shortest and longest visible wave bands from thein situABI dataset to coincident,in situ $K_d\left(\mathrm{P}\mathrm{A}\mathrm{R}\right)$data products. The algorithm was evaluated based on an iterative cross-validation analysis in which 80% of the dataset was randomly partitioned for fitting and the remaining 20% was used for validation. The iteration producing the median coefficient of determination ( $R^2$) value (0.88) resulted in a root mean square difference of $0.319{\mathrm{m}}^{-<\#comment/>1}$, or 8.5% of the range in the validation dataset. Second, coincident mid-day images of central and southern California from ABI and from the Moderate Resolution Imaging Spectroradiometer (MODIS) were compared using Google Earth Engine (GEE). GEE default ABI reflectance values were adjusted based on a near infrared signal. Matchups between the ABI and MODIS imagery indicated similar spatial variability ( $R^2=0.60$) between ABI adjusted blue-to-red reflectance ratio values and MODIS default diffuse attenuation coefficient for spectral downward irradiance at 490 nm, $K_d\left(490\right)$, values. This work demonstrates that if an operational capability to provide ABI aquatic data products was realized, the spectral configuration of ABI would potentially support a sub-hourly, visible aquatic data product that is applicable to water-mass tracing and physical oceanography research. 

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3. Measurement of the e+e− → $$ {B}_s^0{\overline{B}}_s^0X $$ cross section in the energy range from 10.63 to 11.02 GeV using inclusive $$ {D}_s^{+} $$ and D0 production

   https://doi.org/10.1007/JHEP08(2023)131  

   Zhukova, V; Mizuk, R; Adachi, I; Aihara, H; Al_Said, S; Asner, D M; Atmacan, H; Aulchenko, V; Aushev, T; Ayad, R; et al (August 2023, Journal of High Energy Physics)

   A<sc>bstract</sc> We report the first measurement of the inclusivee⁺e⁻→$$ b\overline{b} $$ $b\overline{b}$→$$ {D}_s^{\pm } $$ $D_s^{\pm }$Xande⁺e⁻→$$ b\overline{b} $$ $b\overline{b}$→ D⁰/$$ {\overline{D}}^0 $$ ${\overline{D}}^0$Xcross sections in the energy range from 10.63 to 11.02 GeV. Based on these results, we determineσ(e⁺e⁻→$$ {B}_s^0{\overline{B}}_s^0 $$ $B_s^0{\overline{B}}_s^0$X) andσ(e⁺e⁻→$$ B\overline{B} $$ $B\overline{B}$X) in the same energy range. We measure the fraction of$$ {B}_s^0 $$ $B_s^0$events at Υ(10860) to bef_s= ($$ {22.0}_{-2.1}^{+2.0} $$ ${22.0}_{-2.1}^{+2.0}$)%. We determine also the ratio of the$$ {B}_s^0 $$ $B_s^0$inclusive branching fractions$$ \mathcal{B} $$ $B$($$ {B}_s^0 $$ $B_s^0$→ D⁰/$$ {\overline{D}}^0 $$ ${\overline{D}}^0$X)/$$ \mathcal{B} $$ $B$($$ {B}_s^0 $$ $B_s^0$→$$ {D}_s^{\pm } $$ $D_s^{\pm }$X) = 0.416 ± 0.018 ± 0.092. The results are obtained using the data collected with the Belle detector at the KEKB asymmetric-energye⁺e⁻collider. 

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4. Development of broad modulus profile upon polymer–polymer interface formation between immiscible glassy–rubbery domains

   https://doi.org/10.1073/pnas.2312533120  

   Gagnon, Yannic J; Burton, Justin C; Roth, Connie B (January 2024, Proceedings of the National Academy of Sciences)

   Interfaces of glassy materials such as thin films, blends, and composites create strong unidirectional gradients to the local heterogeneous dynamics that can be used to elucidate the length scales and mechanisms associated with the dynamic heterogeneity of glasses. We focus on bilayer films of two different polymers with very different glass transition temperatures ( $T_{\text{g}}$) where previous work has demonstrated a long-range (∼200 nm) profile in local $T_{\text{g}}\left(z\right)$is established between immiscible glassy and rubbery polymer domains when the polymer–polymer interface is formed to equilibrium. Here, we demonstrate that an equally long-ranged gradient in local modulus $\tilde{G}\left(z\right)$is established when the polymer–polymer interface ( $\approx$5 nm) is formed between domains of glassy polystyrene (PS) and rubbery poly(butadiene) (PB), consistent with previous reports of a broad $T_{\text{g}}\left(z\right)$profile in this system. A continuum physics model for the shear wave propagation caused by a quartz crystal microbalance across a PB/PS bilayer film is used to measure the viscoelastic properties of the bilayer during the evolution of the PB/PS interface showing the development of a broad gradient in local modulus $\tilde{G}\left(z\right)$spanning $\approx$180 nm between the glassy and rubbery domains of PS and PB. We suggest these broad profiles in $T_{\text{g}}\left(z\right)$and $\tilde{G}\left(z\right)$arise from a coupling of the spectrum of vibrational modes across the polymer–polymer interface as a result of acoustic impedance matching of sound waves with $\lambda \sim 5$nm during interface broadening that can then trigger density fluctuations in the neighboring domain. 

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5. Characterizing the fundamental bending vibration of a linear polyatomic molecule for symmetry violation searches

   https://doi.org/10.1088/1367-2630/ace471  

   Jadbabaie, Arian; Takahashi, Yuiki; Pilgram, Nickolas H; Conn, Chandler J; Zeng, Yi; Zhang, Chi; Hutzler, Nicholas R (July 2023, New Journal of Physics)

   Abstract Polyatomic molecules have been identified as sensitive probes of charge-parity violating and parity violating physics beyond the Standard Model (BSM). For example, many linear triatomic molecules are both laser-coolable and have parity doublets in the ground electronic $\tilde{X}{}^2{\mathrm{\Sigma }}^{+}\left(010\right)$state arising from the bending vibration, both features that can greatly aid BSM searches. Understanding the $\tilde{X}{}^2{\mathrm{\Sigma }}^{+}\left(010\right)$state is a crucial prerequisite to precision measurements with linear polyatomic molecules. Here, we characterize the fundamental bending vibration of ${}^{174}$YbOH using high-resolution optical spectroscopy on the nominally forbidden $\tilde{X}{}^2{\mathrm{\Sigma }}^{+}\left(010\right)$ $\to \tilde{A}{}^2{\mathrm{\Pi }}_{1/2}\left(000\right)$transition at 588 nm. We assign 39 transitions originating from the lowest rotational levels of the $\tilde{X}{}^2{\mathrm{\Sigma }}^{+}\left(010\right)$state, and accurately model the state’s structure with an effective Hamiltonian using best-fit parameters. Additionally, we perform Stark and Zeeman spectroscopy on the $\tilde{X}{}^2{\mathrm{\Sigma }}^{+}\left(010\right)$state and fit the molecule-frame dipole moment to $D_{\mathrm{m}\mathrm{o}\mathrm{l}}=2.16\left(1\right)$Dand the effective electrong-factor to $g_S=2.07\left(2\right)$. Further, we use an empirical model to explain observed anomalous line intensities in terms of interference from spin–orbit and vibronic perturbations in the excited $\tilde{A}{}^2{\mathrm{\Pi }}_{1/2}\left(000\right)$state. Our work is an essential step toward searches for BSM physics in YbOH and other linear polyatomic molecules. 

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