Stimulated
emission depletion (STED) nanoscopy plays a key role
in achieving sub-50 nm high spatial resolution for subcellular live-cell
imaging. To avoid re-excitation, the STED wavelength has to be tuned
at the red tail of the emission spectrum of fluorescent probes, leading
to high depletion laser power that might damage the cell viability
and functionality. Herein, with the highly emissive silica-coated
core–shell organic nanoparticles (CSONPs) enabling a giant
Stokes shift of 150 nm, ultralow power STED is achieved by shifting
the STED wavelength to the emission maximum at 660 nm. The stimulated
emission cross section is increased by ∼20-fold compared to
that at the emission red tail. The measured saturation intensity and
lateral resolution of our CSONP are 0.0085 MW cm–2 and 25 nm, respectively. More importantly, long-term (>3 min)
dynamic
super-resolution imaging of the lysosomal fusion–fission processes
in living cells is performed with a resolution of 37 nm.