Topics: Microscopy, Nanotechnology, NEMS, Physics, Research
ABSTRACT
Single-molecule microscopy has become an indispensable tool for biochemical analysis. The capability of characterizing distinct properties of individual molecules without averaging has provided us with a different perspective for the existing scientific issues and phenomena. Recently, super-resolution fluorescence microscopy techniques have overcome the optical diffraction limit by the localization of molecule positions. However, the labeling process can potentially modify the intermolecular dynamics. Based on the highly sensitive nanomechanical photothermal microscopy reported previously, we propose optimizations on this label-free microscopy technique toward localization microscopy. A localization precision of 3 Å is achieved with gold nanoparticles, and the detection of polarization-dependent absorption is demonstrated, which opens the door for further improvement with polarization modulation imaging.
FIG. 2. (a) Schematic of the measurement setup. BE: beam expander. M: mirror. WP: waveplate. LP: linear polarizer. BS: beam splitter. PD: photodetector/power meter. DM: dichroic mirror. ID: iris diaphragm. CCD: charge-coupled device camera. APD: avalanche photodiode detector. (b) The transduction scheme of the trampoline resonator. (c) SEM image of the trampoline resonator.
J. Appl. Phys. 128, 134501 (2020); https://doi.org/10.1063/5.0014905
Nanoelectromechanical photothermal polarization microscopy with 3 Å localization precision, Miao-Hsuan Chien and Silvan Schmid, Journal of Applied Physics
