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The use of S(2)O(8)(2−) and H(2)O(2) as novel specific masking agents for highly selective “turn-on” fluorescent switching recognition of CN(−) and I(−) based on Hg(2+)–graphene quantum dots
In this study, we report that both CN(−) and I(−) can enhance the fluorescent intensity of Hg(2+)–graphene quantum dots (Hg(2+)–GQDs). However, the selectivity of the sensor was poor. Accordingly, simple specific masking agents can be directly used to solve this problem. Here, for the first time, we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077089/ https://www.ncbi.nlm.nih.gov/pubmed/35540915 http://dx.doi.org/10.1039/c7ra12327b |
Sumario: | In this study, we report that both CN(−) and I(−) can enhance the fluorescent intensity of Hg(2+)–graphene quantum dots (Hg(2+)–GQDs). However, the selectivity of the sensor was poor. Accordingly, simple specific masking agents can be directly used to solve this problem. Here, for the first time, we report the use of persulfate ion (S(2)O(8)(2−)) as a turn-on fluorescent probe of Hg(2+)–GQDs for selective CN(−) detection, while hydrogen peroxide (H(2)O(2)) was selected for its sensing ability towards I(−) ion detection. Interestingly, the signal was immediately measured after addition of the masking agent to Hg(2+)–GQDs and the sample because its interaction was very fast and efficient. The method had a linear response in the concentration ranges of 0.5–8 μM (R(2) = 0.9994) and 1–12 μM (R(2) = 0.9998) with detection limits of 0.17 and 0.20 μM for CN(−) and I(−), respectively. The sensor was successfully used for the dual detection of both CN(−) and I(−) in real water samples with satisfactory results. In conclusion, the specific masking agents in a Hg(2+)–GQDs system appeared to be good candidates for fluorometric “turn-on” sensors for CN(−) and I(−) with excellent selectivity over other ions. |
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