4,218 publications from this institution
AbstractThe neutron spectra and ambient dose equivalent were determined by unfolding measured Bonner sphere system data using different unfolding methods. These methods included a maximum entropy method (MAXED code), nonlinear least-squares method (GRAVEL code) with several different starting spectra, and a genetic algorithm method. These algorithms were used to unfold measured Bonner sphere data that had been collected using a LiI(Eu) detector and activation foils. The Bonner sphere system was exposed to neutrons from a known AmBe source and at the proton accelerator facility at the University of Texas M. D. Anderson Cancer Center. The total fluence rates and total ambient dose equivalents of the neutron field agree within 7.5%, regardless of unfolding algorithm or starting spectrum. In contrast, the fluence-weighted average energy varied dramatically, depending on the starting spectrum used in the unfolding process. These findings offer insight and guidance into the use of unfolding algorithms and starting spectra for neutron spectroscopy.
We successfully developed an approach to synthesize a metal oxide- and N-codoped carbon nanosheet, NC@CoO/CuO, derived from a metal-organic framework nanofiber, Cu(ii)-Asp@Co(II) (Asp = l-aspartate). The use of NC@CoO/CuO as a high-performance catalyst for the oxygen evolution reaction in water splitting has also been demonstrated.
There are two mass diffusion processes regarding the vapor-liquid-solid (VLS) growth of nanostructures: one is inside the catalyst droplet toward the liquid-solid interface; the other is along the side surface planes of the growing nanostructures. In this letter, microscale, modulated mass diffusion scenarios are exhibited through the synthesis of two types of ZnS nanostructures in an Au-catalyzed VLS process: periodically twinned nanowires originated from periodical fluctuation between diffusion rate inside the catalytic droplet and the growth rate on the liquid-solid interface; the formation of asymmetrically polytypic nanobelts is related to one certain side surface bounded by high surface-energy plane, which serves as a preferential diffusion direction of reactant adatoms. The results may have important impact on the understanding of the physical and chemical process of the VLS mechanism. These longitudinally and latitudinally tunable crystalline structures enrich the family of one-dimensional nano-building blocks, and may find potential applications in nanotechnology.