Harsh Bais, PhD



Fluorescence lifetime imagers


Traditional Fluorescence Lifetime Imaging Microscopy systems use laser scanning techniques in concert with a single photon detector, such as a photomultiplier tube or avalanche photodiode, to construct lifetime based images using Time Correlated Single Photon Counting (TCSPC).  In order to acquire enough data within each pixel to determine the lifetime, thousands of samples must be taken.  As a result, the time required to capture a single frame can be several to tens of seconds, which presents a limit to the types of biological processes that can be monitored using FLIM.  The focus of this project is creating a CMOS-based Single Photon Avalanche Diode (SPAD) array that is capable of acquiring multiple frames per second, which would make real-time FLIM imaging of biological processes possible.

Our most recent array design was capable of a maximum frame rate of 3.9 Hz and consisted of a 64 x 64 SPAD array with integrated timing and pixel control circuitry in 0.35μm technology. The image on this page below shows a FLIM image of quantum dots (in color) next to a CCD image showing the location of the quantum dots on the array.

Our recent efforts are focused on developing a SPAD array in a standard CMOS process flow for a more advanced technology node. We have developed a low-noise SPAD in 0.13μm technology that will enable higher imaging rates through improved circuit performance. A full imaging array based on this SPAD design is currently under development.