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distribution. For ideal sources and optical surfaces we can solve the so-called Monge-Ampère equation to find the freeform shapes of the surfaces. Scattering elements however send light rays in multiple
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-ray Photon Correlation Spectroscopy (XPCS), Quasi-Elastic Neutron Scattering (QENS) and Dynamic Light Scattering (DLS) techniques to study the structure and dynamics of proteins in solutions
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Correlation Spectroscopy (XPCS), Quasi-Elastic Neutron Scattering (QENS) and Dynamic Light Scattering (DLS) techniques to study the structure and dynamics of proteins in solutions. Qualification and skills
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-ray Photon Correlation Spectroscopy (XPCS), Quasi-Elastic Neutron Scattering (QENS) and Dynamic Light Scattering (DLS) techniques to study the structure and dynamics of proteins in solutions
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-ray Photon Correlation Spectroscopy (XPCS), Quasi-Elastic Neutron Scattering (QENS) and Dynamic Light Scattering (DLS) techniques to study the structure and dynamics of proteins in solutions. Your tasks
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scattering, neutron scattering, light scattering and fluorescence microscopy to unravel the properties of such droplets. The concrete activities during the project will involve protein handling, general
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of Mathematics at Radboud University (Nijmegen, Netherlands), and join the research group of Laura Scarabosio, funded by the NWO Vidi programme ’Taming Frequency in Bayesian Inverse Wave Scattering’. Inverse wave
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scattering (SERS) and infrared (IR) spectroscopy will be employed to probe vibrational signatures, revealing structural changes and interactions at the single-molecule level [1-5]. A significant aspect of the
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qualifications. Possible topics are: The theory of ultrafast pump-probe experiments (e.g., time-resolved X-ray scattering and spectroscopy), simulations and data processing of actual ultrafast experiments, mapping
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University of Göttingen (Germany) and the European Synchrotron (ESRF) in Grenoble (France), we will design and build a novel synchrotron setup to combine x-ray scattering with light microscopy. The newly built