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nanoscale structure using TEM, AFM, FRET, DIB, etc. W design the amino-acid sequence of the IDPs and TRs de novo from the bottom up and study these in biomimetic nanopores. The approach can be expected
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a liposome from a sphere- to a dumbbell shape. Using biophysical tools (fluorescence, AFM, TEM,..), we will study the CdvABC proteins from an archaeum that lives at room temperature. We will study
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-situ spectroscopic and microscopic methods, including XRD, Raman spectroscopy, TEM, and XPS. Evaluating catalytic performance for various electrochemical reactions, such as the oxygen reduction reaction
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on conventional transmission electron microscopy (TEM) exposures taken in underfocus. In this project, we aim to further develop the imaging analysis capabilities for (scanning) transmission electron microscopy
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, hysteresis, oscillatory behaviour and support dependencies. Compare cluster behaviour across different characterization techniques (TEM, STM, TPD). Integrate findings to map the relationship between cluster
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technologies, physicochemical characterization of nanomaterials, using techniques such as SEM, TEM, DLS, XPS. Solid experience with electroanalytical techniques for characterization of the electrochemical
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electron microscopy using a transmission electron microscopy (TEM) and a scanning electron microscopy (SEM). Experience developing new or existing electron microscopy instrumentation or methods. Significant
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-TEM. · The Department of Biochemistry provides a rich intellectual environment, with research in structural biology (cryo-EM, X-ray crystallography, NMR spectroscopy), and computational biology
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: electrode/device fabrication using inkjet printing including rheolgy characterization, physicochemical characterization of nanomaterial, using techniques such as SEM, TEM, DLS, XPS. Solid experience with
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Your Job: Synthesis of heterogeneous catalysts (Ni on Al2O3) and characterization involving e.g. TGA, IR, TEM, MS, BET Implementation of a reaction chamber for catalytic measurements into a