Room temperature phosphorescence (RTP) as a fascinating phenomenon shows great potential toward multiple applications. Howbeit, it is challengeable to improve the phosphorescence efficiency of carbon dots (CDs) owing to their short lifetime. Herein, we proposed a facile, rapid, and gram-scale strategy to synthesize the cross-linked carbon dots (named N-CDs) with both bright blue fluorescence and green RTP emissions. To be specific, the polymer of polyethylenimine (PEI) served as the cross-linking agent and carbon source, during which process phosphoric acid accelerated the formation of the compact carbon core within 30 s. Subsequently, the cross-linked carbon dots with the rigid network formed a small singlet-triplet energy splitting (ΔEST) of 0.490 eV, thus exhibiting a long RTP lifetime of 429.880 ms while coated on the filter paper through the hydrogen bonds. Taking advantage of the double luminescence, we successfully achieved the dual-channel detection of promethazine by N-CDs. The fluorescence of N-CDs was obviously quenched by promethazine through the electron-transfer process, displaying the linear range from 0.4 to 8 mM. Significantly, the electron transfer (ET) from carbon dots to promethazine boosted their phosphorescence efficiency and prolonged the lifetime to 565.190 ms, and the enhanced phosphorescence facilitated the sensitive recognition of promethazine with the concentration range of 1-3000 μM. Meanwhile, the possible autofluorescence interference from biological samples could be avoided through this RTP assaying mode, providing the more accurate results. Also, their RTP and fluorescence endowed the current N-CDs with the ability of dual-signal painting and imaging. This strategy may broaden the new approaches to produce the long-lifetime and high-efficiency RTP material toward the sensing purpose.
Keywords: carbon dots; electron transfer; fluorescence quenching; phosphorescence enhancing; promethazine detection.