Photostable and printable fluorescence carbon quantum dots for advanced message encryption and specific reversible multiple sensing of Cu2+ and cysteine

荧光 碳量子点 加密 量子点 化学 半胱氨酸 碳纤维 纳米技术 材料科学 计算机科学 光化学 有机化学 算法 计算机安全 光学 物理 复合数
作者
Hui Li,Tiantian Xu,Zhe Zhang,Jiao Chen,Mengyao She,Yali Ji,Boyue Zheng,Zheng Yang,Shengyong Zhang,Jianli Li
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:453: 139722-139722 被引量:72
标识
DOI:10.1016/j.cej.2022.139722
摘要

• Carbon quantum dots sensor is presented for mapping and removing Cu 2+ and Cysteine. • The sensor displays significant selectivity, sensitivity and fluorescent stability. • The selectivity sensing is mechanism clarified as the on-off-on process. • Information encryption and fluorescent printing are successfully performed. • The sensor is promising for biological detection with negligible cytotoxicity. The ability to manipulate carbon quantum dots (CQDs) fluorescence with specific substances has been of primary importance for applications in advanced dynamic information encryption. The development of CQDs with specific functionalization, high selectivity and excellent fluorescence stability for information security and sensing remains a challenge. In this paper, we present an N-doped and tryptophan functionalized CQDs that can be applied not only as a fluorescent ink for multiple message encryption but also for fluorescent sensitive and selective recognition of Cu 2+ and cysteine (Cys) by multi-method, including aqueous solutions, filter paper, hydrogels and in human DU-145 Prostate cancer cells. Theoretical calculations and mechanistic studies suggested that this on-off-on mechanism was attributed to the transfer of electrons between Cu 2+ and functionalized groups on the surface of CQDs and stronger coordination capability with Cys. The above results showed that these newly designed CQDs will greatly enrich the fundamental understanding of CQDs by explaining the recognition mechanism between Cu 2+ and Cys, and provide an opportunity for anti-counterfeiting, solid-state fluorescent materials, cellular imaging and environmental.
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