Publications

Summary Large numbers of supernovae (SNe) have been discovered in recent years, and many more will be found in the near future. Once discovered, further study of a SN and its possible use as an astronomical tool (e.g., as a distance estimator) require knowledge of the SN type. Current classification methods rely almost solely on the analysis of SN spectra to determine their type. However, spectroscopy may not be possible or practical. We present a classification method for SNe based on the comparison of their observed colors with synthetic ones, calculated from a large database of multi-epoch optical spectra of nearby events. Broadband photometry at optical wavelengths allows classification of SNe up to z = 0.75, and the use of infrared bands extends it further to z = 2.5. We demonstrate the applicability of this method, outline the observational data required to further improve the usefulness of the method, and discuss prospects for its use on future SN samples. Community access to the tools developed is provided by a dedicated website.

We experimentally demonstrate 204x spontaneous emission rate enhancement from an electrically-injected nanoLED coupled to a cavity-backed optical slot antenna. This places the spontaneous emission rate on par with the stimulated emission rate.

Gas-diffusion electrodes (GDEs) for electrochemical CO2 reduction allow for an order-of-magnitude increase in obtainable limiting current densities (~100 mA/cm2) compared to planar systems (~10 mA/cm2) due to the increase in CO2 flux, catalyst surface area, and reduction in diffusion length. Despite this improvement, aqueous GDE systems suffer from extensive catalyst dissolution/delamination and membrane degradation under operating conditions, as well as exhibit significant ohmic resistances stemming from their electrolyte layers. These characteristics limit the current densities that can be achieved at applied overpotentials and render them impractical for industrial implementation. Membrane-electrode assemblies (MEAs), consisting of humidified gaseous feeds at one or both electrodes and no aqueous electrolyte between the electrodes (i.e. only using a solid ion-conducting polymer or ionomer as an electrolyte), can overcome the limitations of the aqueous GDE. In this poster, two MEA cell designs will be addressed: Full-MEA (humidified gaseous feeds at both the anode and cathode) and Exchange-MEA (humidified gaseous feed at the cathode and an adjoining water or salt solution, e.g. KHCO3 or KOH, at the anode to provide hydration and a source of ions). The experimental performance results obtained from the near-optimized vapor-fed Full-MEA and H2O Exchange-MEA systems for CO2RR at ambient temperature and pressure conditions and the details of our ongoing work in building a fully integrated, tandem/cascade catalysis device are described. This poster also details plans for future investigations in exploring critical fabrication, operating conditions, and MEA properties. Acknowledgements This material is based upon work performed by the Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub, supported through the Office of Science of the U.S. Department of Energy under Award Number DE-SC0004993. We would also like to thank Nemanja Danilovic, Kun Jiang, Julie Fornaciari, Yagya Regmi, Douglas Kushner, and Christianna Lininger for their help, discussions, and guidance in the course of this research project.

Introduction While the anti-resorptive effects of the bisphosphonates (BPs) are well documented, many questions remain about their mechanisms of action, particularly following long-term use. This study evaluated the effects of alendronate (Ale) treatment on TGF-β1 signaling in mesenchymal stem cells (MSCs) and osteocytes, and the relationship between prolonged alendronate treatment on systemic TGF-β1 levels and bone strength. Methods TGF-β1 expression and signaling were evaluated in MSCs and osteocytic MLO-Y4 cells following Ale treatment. Serum total TGF-β1 levels, a bone resorption marker (DPD/Cr), three-dimensional microCT scans and biomechanical tests from both the trabecular and cortical bone were measured in ovariectomized rats that either received continuous Ale treatment for 360days or Ale treatment for 120days followed by 240days of vehicle. Linear regression tests were performed to determine the association of serum total TGF-β1 levels and both the trabecular (vertebrae) and cortical (tibiae) bone strength. Results Ale increased TGF-β1 signaling in the MSCs but not in the MLO-Y4 cells. Ale treatment increased serum TGF-β1 levels and the numbers of TGF-β1-positive osteocytes and periosteal cells in cortical bone. Serum TGF-β1 levels were not associated with vertebral maximum load and strength but was negatively associated with cortical bone maximum load and ultimate strength. Conclusions The increase of serum TGF-β1 levels during acute phase of estrogen deficiency is likely due to increased osteoclast-mediated release of matrix-derived latent TGF-β1. Long-term estrogen-deficiency generally results in a decline in serum TGF-β1 levels that are maintained by Ale treatment. Measuring serum total TGF-β1 levels may help to determine cortical bone quality following alendronate treatment.

Adolescence is a developmental period characterized by a greater tendency to take risks. While the adult literature has shown that sex steroids influence reward-related brain functioning and risk taking, research on the role of these hormones during puberty is limited. In this study, we examined the relation between pubertal hormones and adolescent risk taking using a probabilistic decision-making task. In this task, participants could choose on each trial to play or pass based on explicit information about the risk level and stakes involved in their decision. We administered this task to 58 11-to-13-year-old girls while functional MRI images were obtained to examine reward-related brain processes associated with their risky choices. Results showed that higher testosterone levels were associated with increased risk taking, which was mediated by increased medial orbitofrontal cortex activation. Furthermore, higher estradiol levels were associated with increased nucleus accumbens activation, which in turn related to decreased risk taking. These findings offer potential neuroendocrine mechanisms that can explain why some adolescent girls might engage in more risk taking compared to others.

The utility of the method is demonstrated by the formal synthesis of (-)-isocynometrine (XVI) via pyrrolidine (XIVa).