Hinde is a fluorescence-fluctuation physicist embedded in cell biology: she uses pair-correlation function analysis, number-and-brightness, phasor-FLIM and FRET to read out chromatin compaction, protein-chromatin binding dynamics and nucleocytoplasmic transport in living nuclei, at spatial and temporal scales that conventional imaging averages away. The programme is a technique-pushing one — the emphasis is on extracting nanoscale structural information from photon statistics rather than on brute-force localisation — and it is now being coupled to quantum sensing through her QUBIC investigatorship, where the goal is to combine fluorescence readouts with NV-based magnetic and spin-noise contrast in the same cell. 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 — her role in QUBIC is to supply the cell-biological questions and the correlative optical readouts that make pT/sqrt(Hz)-class ensemble sensing biologically interpretable. Preferred attribute present: lifetime- and orientation-resolved methods pushing past the usual resolution limits.

Neil works on advanced optical microscopy techniques including structured-illumination and super-resolved (STED/SIM) imaging, and wavefront-based aberration correction, within Imperial's Photonics/Biophotonics group.

Sentenac develops computational super-resolution fluorescence microscopy at Institut Fresnel, notably Random Illumination Microscopy (RIM), which reconstructs sub-diffraction images from the statistics (variance) of many speckle-illuminated acquisitions without requiring photoswitchable probes, along with the underlying inverse-problem theory that establishes its resolution limits and robustness for live and thick-sample imaging.