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Ultrafast lasers have found increasing use in scanning optical microscopy because of its very high peak power in generating multiphoton optical excitations. We are demonstrating that the multiphoton processes can be further extended to third harmonic generation (THG) and two-photon (2-p) excitation in the UVB range with broader tunability enabled by a synchronously pumped optical parametric oscillator (OPO). The scanning nature of image acquisition process also greatly facilitates the incorporation of techniques in signal processing, which opens further possibilities. For example, the very short pulse width of ultrafast lasers allows excitation and sampling of photo-processes with extremely broad bandwidth. As such, radio frequency is excited as a contrast signal in imaging high speed photodiodes. In addition, dithering techniques that base on lock-in detection allows signal conditioning so that better signal to noise ratio can be resulted and features of high spatial frequency can be emphasized.
Fu-Jen Kao
"The use of advanced light source and signal processing in scanning optical microscopy", Proc. SPIE 5255, Biomolecular Photonics and Multidimensional Microscopy, (4 December 2003); https://doi.org/10.1117/12.546235
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Fu-Jen Kao, "The use of advanced light source and signal processing in scanning optical microscopy," Proc. SPIE 5255, Biomolecular Photonics and Multidimensional Microscopy, (4 December 2003); https://doi.org/10.1117/12.546235