443 structures "https:" "https:" "https:" "https:" "https:" "https:" "https:" "https:" "https:" PhD scholarships at University of Jena Cluster of Excellence "Balance of the Microverse"
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and Simulation Group at ICN2 conducts cutting-edge research in computational materials science, focusing on electronic structure methods, atomistic simulations, and multiscale modelling. The group
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epitaxy-pulsed laser deposition (MBE-PLD) technique. Careful study of the structure of this film by XRD, XPS, and TEM (collaboration with Prof. M Seibt / Dr. T. Meyer, University of Göttingen) and analysis
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wide range of career opportunities in science, technology, and administration. The position is located at the Institute for Nuclear Physics. The research focus lies on the structure of atomic nuclei
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XFEL. About your role: Application of storage-ring and FEL-based X-ray scattering methods to BlueMat topics (such as role of confined geometries on structure and dynamics on liquids) In particular
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Identifying and validating models for complex structures featuring nonlinearity remains a cutting-edge challenge in structural dynamics, with applications spanning civil structures, microelectronics
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steps in Hamburg, please see: https://www.uni-hamburg.de/piasta/beratung/doc/willkommen.pdf . Structured research and supervision Yes Research training / discussion Yes Support for international students
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– we support you specifically and individually e.g., through training and networking opportunities specifically for doctoral candidates (JuDocS): https://go.fzj.de/JuDocs SUPPORT FOR INTERNATIONAL
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related field Practical experience in organic synthesis chemistry and peptide chemistry Knowledge in structural analysis (NMR, UV, HPLC, ITC) Willingness to work with radioactive substances Practical
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applications in information technology and are based on electrical, magnetic or optical functionalities. The Department of Quantum Technologies is looking for a PhD Student (f/m/d) - Imaging magnetic structures
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drugs. To solve this problem, this project will investigate if allosteric inhibitors can be designed towards a number of transporters sharing the same protein structure folds (the LeuT-fold). The chosen