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DTSTART;TZID="Pacific Time (US & Canada)":20220401T161000
DTEND;TZID="Pacific Time (US & Canada)":20220401T170000
SUMMARY:Physical Chemistry Seminar — Shinhyo Bang
LOCATION:Fulmer Hall
DESCRIPTION:Title: Size-dependent surface structure of COF-embedded UO2 nanoparticles\n\nAbstract: Characterization of actinide oxides at the nanoscale presents unique challenges due to their radioactivity, high surface area, and inherent diffraction broadening due to small grain size. Extended x-ray absorption spectroscopy (EXAFS) is an analytical method to investigate atomic-scale structural properties that enables their encapsulation and does not rely on long-range order. There is a limitation that EXAFS only gives the averaged structural information of heterogeneous samples. We aimed to deconvolute EXAFS results to extract the surface coordination environment of UO2 NPs by proper modeling, and investigate how it evolves with varying sizes (1.4, 4.7, 8 nm). The termination effect was used to quantify the surface terminating species of UO2 NPs. A higher degree of oxygenation on the surface was observed for 8 nm NPs. EXAFS simulation was implemented to backtrack the surface structure of these NPs. It was observed that the bond contraction due to the surface relaxation effect was localized in a few outermost layers of NPs and the surface disorder of 1.4 and 4.7 nm NPs was significantly enhanced from that of bulk.
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