By only replacing phenylg roup with N-methylpyridinium in a2 -(2-hydroxyphenyl)benzothiazole (HBT) derivative HBT-s-Ph, which is an excited state intramolecular protont ransfer (ESIPT)-active dye, the conjugated HBT-N-methylpyridinium hybrid HBT-Py,e mits high-efficiency fluorescence (F f :2 9%)w ith an exceedingly large Stokes shift (213 nm) even in aqueous solution. Emission spectroscopy and computational calculations indicate that this typical photophysical property owes to low-barrier Hbond (LBHB)-assisted internal charge transfer (ICT), not ESIPT.