Salt-resistant nanosensor for fast sulfadimethoxine tracing based on oxygen-doped g-C3N4 nanoplates

磺胺二甲氧嘧啶 纳米传感器 纳米化学 荧光 检出限 电子转移 兴奋剂 化学 纳米技术 猝灭(荧光) 纳米材料 纳米器件 分析化学(期刊) 光化学 材料科学 化学工程
作者
Qiusu Wang,Chenmin Xu,Huan He,Xing Zhang,Lei Lin,Guoxiang Wang
出处
期刊:Mikrochimica Acta [Springer Nature]
标识
DOI:10.1007/s00604-021-04800-6
摘要

A novel oxygen-doped g-C3N4 nanoplate (OCNP) structure that can serve as an efficient sulfadimethoxine (SDM) sensing platform has been developed. Taking advantage of its inherent oxygen-containing functional groups and 2D layered structure with π-conjugated system, OCNP exhibits effective radiative recombination of surface-confined electron-hole pairs and efficient π-π interaction with SDM. This causes rapid fluorescence response and thus ensures the fast and continuous monitoring of SDM. Based on the fluorescence experiments and band structure calculation, the mechanism of the SDM-induced quenching phenomenon was mainly elucidated as the photoinduced electron transfer process under a dynamic quenching mode. Under optimized conditions, the as-proposed nanosensor, which emitted strong fluorescence at 375 nm with an excitation wavelength at 255 nm, presents an excellent analytical performance toward SDM with a wide linear range from 3 to 60 μmol L-1 and a detection limit of 0.85 μmol L-1 (S/N = 3). In addition, this strategy exhibits satisfactory recovery varied from 94 to 103% with relative standard derivations (RSD) in the range 0.9 to 6.8% in real water samples. It also shows marked tolerability to a series of high concentrations of metals and inorganic salts. This strategy not only broadens the application of oxygen-doped g-C3N4 nanomaterial in antibiotic sensing field but also presents a promising potential for on-line contaminant tracing in complex environments.

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