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Abstract Zero‐dimensional (0D) hybrid metal halides have been emerged as room‐temperature phosphorescence (RTP) materials, but synchronous optimization of multiple phosphorescence performance in one structural platform remains less resolved, and stable RTP activity in aqueous medium is also unrealized due to serious instability toward water and oxygen. Herein, we demonstrated a photophysical tuning strategy in a new 0D hybrid zinc halide family of (BTPP) 2 ZnX 4 (BTPP=benzyltriphenylphosphonium, X=Cl and Br). Infrequently, the delicate combination of organic and inorganic species enables this family to display multiple ultralong green afterglow and efficient self‐trapped exciton (STE) associated cyan phosphorescence. Compared with inert luminescence of BTPP + cation, incorporation of anionic ZnX 4 2− effectively enhance the spin‐orbit coupling effect, which significantly boosts the photoluminescence quantum yield (PLQY) up to 30.66 % and 54.62 % for afterglow and phosphorescence, respectively. Synchronously, the corresponding luminescence lifetime extend to 143.94 ms and 0.308 μ s surpassing the indiscernible phosphorescence of BTPPX salt. More importantly, this halide family presents robust RTP emission with nearly unattenuated PLQY in water and harsh condition (acid and basic aqueous solution) over half a year. The highly efficient integrated afterglow and STE phosphorescence as well as ultrahigh aqueous state RTP realize multiple anti‐counterfeiting applications in wide chemical environments.
Zhao et al. (Sat,) studied this question.