Pb2+ codoping enhances the Tb3+ emission
in trivalent terbium-doped zinc sulfide [Zn(Tb)S] nanoparticles (NPs).
The Tb3+-Pb2+ spatial proximity and a favorable
codopant electronic energy level alignment contribute toward this
emission brightening. This work tests the performance of the Tb3+ emission in the Zn(TbPb)S and Zn(Tb)S/Pb NPs, where the
dopants within parentheses and after slashes indicate their synthetic
and postsynthetic doping, respectively. When screened against steady-state
and time-resolved photoluminescence, photoelectron spectroscopy, zeta
potential, and infrared absorption of surface capping ligands, the
Zn(TbPb)S NPs emerge as a superior sensitizer to generate Tb3+ emission. A core dominant Tb3+-Pb2+ interaction
in Zn(TbPb)S NPs prompts a stronger Tb3+ emission when
compared to the surface dominant Tb3+-Pb2+ interaction
in Zn(Tb)S/Pb NPs. This doping strategy guided the NP design principle to control lanthanide
emission, which expands the palette of lanthanide-based NP luminophores
for practical applications. The Pb2+‑sensitized
Tb3+ emission brightening in the ZnS NPs in the precation
exchange reaction conditions can find applications in Pb2+ sensing, cellular imaging, and light emitting diodes (LEDs).