Uses X-ray photoemission electron microscopy (X-PEEM) with XANES spectroscopy at synchrotron light sources to map crystal orientation and amorphous-to-crystalline transitions at ~10 nm resolution in biominerals (coral skeletons, sea urchin spines, mollusk nacre, tooth enamel).
Gureyev is one of the originators of propagation-based X-ray phase-contrast imaging and the transport-of-intensity phase-retrieval methods that made it practical; his current work concerns the information-theoretic limits of imaging — how signal-to-noise, spatial resolution and radiation dose trade against one another — and the application of those limits to phase-contrast tomography, ptychography and electron microscopy, including biomedical imaging at clinically tolerable dose. Positioned against the established body of NV-ensemble quantum sensing work — DEER, nanoscale NMR and T1 relaxometry protocols operating at pT/sqrt(Hz) field sensitivity — the shared intellectual core is the noise-resolution-dose triangle: the same estimation-theory framework that sets the pT/sqrt(Hz) floor of an NV ensemble governs how many photons a phase-contrast image needs. Borderline inclusion (X-ray rather than quantum sensing), kept because the technique is explicitly about pushing resolution past conventional limits.
Jacob Hoogenboom develops integrated correlative light and electron microscopy (CLEM) and molecular nanophotonic imaging. Research: (1) 3-in-1 microscopy combining light, electron beam, and ion beam for precise biological sample sectioning and protein localisation; (2) integrated CLEM for mapping proteins in cellular context; (3) single-molecule nanophotonic sensing using fluorescence. Relevant to advanced single-molecule biosensing approaches.
Prof. Jacobsen's group develops novel methods, instruments, and analysis approaches for X-ray nanoscale imaging and applies them to biology and environmental science, using the Advanced Photon Source (APS) at Argonne. Directions: (1) Scanning X-ray fluorescence microscopy (SXFM) for organ-wide and nanoscale elemental mapping of metals (zinc, copper, iron) in biological tissues — central to the NIH-funded QE-Map national resource; imaging how metals regulate cellular functions, synaptic zinc signaling, and neurodegenerative disease; (2) X-ray ptychography and coherent diffractive imaging (CDI) for nanoscale biological imaging beyond the diffraction limit with improved dose efficiency; (3) Development of new algorithms, optics (zone plates), and detector systems to push spatial resolution and dose efficiency in X-ray microscopy — including lensless imaging methods and compressed-sensing reconstruction. Joint appointment at Argonne National Laboratory (Argonne Distinguished Fellow); also involved in QE-Map resource with Kozorovitskiy and Hao Zhang (McCormick).
Willem Vanderlinden uses high-resolution biophysical tools to study protein-nucleic acid interactions. Research: (1) magnetic tweezers for pN-scale force and torque measurements on single DNA molecules and nucleoprotein complexes during retroviral integration, DNA supercoiling, and chromatin remodelling; (2) high-speed AFM imaging of nucleoprotein complexes and chromosomal organisation; (3) quantitative single-molecule statistical analysis of DNA topology. His approach provides cutting-edge spatial resolution to study chromatin biophysics and mobile DNA elements at the single-molecule level.