The doping of carbon quantum dots with nitrogen provides a promising direction to improve fluorescence performance and broaden their applications in sensing systems. Herein we report a one-pot solvothermal synthesis of N-doped carbon quantum dots (NCQDs) and the synthesis of a series of NCQDs with different nitrogen contents. The as-prepared NCQDs were compared with carbon quantum dots (CQDs); the introduction of nitrogen atoms largely increased the quantum yield of NCQDs and highest emission efficiency is up to 36.3 %. The fluorescence enhancement may originate from more polyaromatic structures induced by incorporated nitrogen atoms and protonation of nitrogen atoms on dots. It was found that NCQDs can act as a multifunctional fluorescence sensing platform because they can be used to detect pH values, Ag(I), and Fe(III) in aqueous solution. The fluorescence intensity of NCQDs is inversely proportional to pH values across a broad range from 5.0 to 13.5, which indicates that NCQDs can be devised as an effective pH indicator. Selective detection of Ag(I) and Fe(III) was achieved based on their distinctive fluorescence influence because Ag(I) can significantly enhance the fluorescence whereas Fe(III) can greatly quench the fluorescence. The quantitative determination of Ag(I) can be accomplished with NCQDs by using the linear relationship between fluorescence intensity of NCQDs and concentration of Ag(I). The sensitive detection of H2O2 was developed by taking advantage of the distinct quenching ability of Fe(III) and Fe(II) toward the fluorescence of NCQDs. Cellular toxicity test showed NCQDs still retain low toxicity to cells despite the introduction of a great deal of nitrogen atoms. Moreover, bioimaging experiments demonstrated that NCQDs have stronger resistance to photobleaching than CQDs and more excellent fluorescence labeling performance.
Heteroatom doping of carbon quantum dots not only enables great improvement of fluorescence efficiency and tunability of fluorescence emission, but also provides active sites in carbon dots to broaden their application in sensor. Silicon as a biocompatible element offers a promising direction for doping of carbon quantum dots. Si-doped carbon quantum dots (SiCQDs) were synthesized through a facile and effective approach. The as-prepared Si-doped carbon quantum dots possess visible fluorescence with high quantum yield up to 19.2%, owing to fluorescence enhancement effect of introduced silicon atoms into carbon dots. The toxicity test on human Hela cells showed that SiCQDs have lower cellular toxicity than common CQDs, and bioimaging experiments clearly demonstrated their excellent biolabelling ability and outstanding performance in resistance to photobleaching. Strong fluorescence quenching effect of Fe(III) on SiCQDs can be used for its selective detection among general metal ions. Specific electron transfer between SiCQDs and hydrogen peroxide enables SiCQDs as a sensitive fluorescence sensing platform for hydrogen peroxide. The subsequent fluorescence recovery induced by removal of hydrogen peroxide from SiCQDs due to formation of the stable adducts between hydrogen peroxide and melamine was taken advantage of to construct effective sensor for melamine.
Fluorescent B-doped carbon quantum dots (BCQDs) were prepared by a facile one-pot solvothermal route. The BCQDs can be used as a novel fluorescence sensing system for hydrogen peroxide and glucose detection.
A novel and efficient fluorescence sensing platform based on biocompatible graphene quantum dots and graphene oxide was established. It showed high selectivity and sensitivity for DNA detection.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.