In any image, the number of detected probe particles is fundamentally limited, either due to finite acquisition times or  probe-induced sample damage. In order to optimize the sensitivity of a microscope, the information that can be extracted from each detected probe particle has to be maximized.  We achieve this by employing cavity enhancement, quantum enhancement, and wave-front shaping techniques.


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We are happy to announce that Clara received a fellowship from the FFG to continue her research on high-sensitivity multi-pass microscopy for protein...


Ein Mikroskop aus Licht

Our work was featured by the uni:view Magazin.


Philip Weber is currently finishing his PhD on 2D Paul traps for electrons in the Hommelhoff group at FAU Erlangen. He will strengthen our electron...