{"title":"Dual-mode ratiometric fluorescent and colorimetric sensor for rapid visual detection of Hg<sup>2+</sup> using poly(T)-tailed ssDNA-silver nanoclusters.","authors":"Yu Zou, Ying Zhang, Hui Zhu Wang, Meng Wei Jiang, Guo Feng Gui, Dong Fu, Wang Ren","doi":"10.1016/j.saa.2025.125751","DOIUrl":null,"url":null,"abstract":"<p><p>Rapid, sensitive, and accurate detection of heavy metal ions is significant for human health and ecological security. Herein, a novel single-stranded DNA with poly(thymidine) tail is tactfully designed as template to synthesize dual-emission silver nanoclusters (ssDNA-AgNCs). The obtained AgNCs simultaneously emit red and green fluorescence, and the red emission can be selectively quenched by Hg<sup>2+</sup>, meanwhile the green emission of AgNCs increases synchronously. Thus ssDNA-AgNCs as a single probe shows excellent ratiometric fluorescence sensing for Hg<sup>2+</sup> with a detection limit of 0.2 nM, and Hg<sup>2+</sup> as low as 10.0 nM can be fluorescently identified by naked eye within 5 min. Moreover, the proposed nanoprobe also exhibits a good ratiometric colorimetric sensing for Hg<sup>2+</sup>, and the obvious color change of nanoprobe also enables a rapid and visual monitoring of Hg<sup>2+</sup> under visible light. The dual mode ratiometric response of Hg<sup>2+</sup> can be ascribed to the rapid redox reaction between Hg<sup>2+</sup> and Ag<sup>0</sup> on the surface of AgNCs and the subsequent formation of silver amalgam. The resultant dual-mode ratiometric sensor has been successfully applied to the determination of Hg<sup>2+</sup> in environmental water samples. This study provides a new strategy to synthesize dual-emission AgNCs by scientifically designing terminus sequence of ssDNA template, and develops a facile and efficient single-probe and dual-mode ratiometric sensor for visual monitoring of Hg<sup>2+</sup>.</p>","PeriodicalId":94213,"journal":{"name":"Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy","volume":"330 ","pages":"125751"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.saa.2025.125751","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/15 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Rapid, sensitive, and accurate detection of heavy metal ions is significant for human health and ecological security. Herein, a novel single-stranded DNA with poly(thymidine) tail is tactfully designed as template to synthesize dual-emission silver nanoclusters (ssDNA-AgNCs). The obtained AgNCs simultaneously emit red and green fluorescence, and the red emission can be selectively quenched by Hg2+, meanwhile the green emission of AgNCs increases synchronously. Thus ssDNA-AgNCs as a single probe shows excellent ratiometric fluorescence sensing for Hg2+ with a detection limit of 0.2 nM, and Hg2+ as low as 10.0 nM can be fluorescently identified by naked eye within 5 min. Moreover, the proposed nanoprobe also exhibits a good ratiometric colorimetric sensing for Hg2+, and the obvious color change of nanoprobe also enables a rapid and visual monitoring of Hg2+ under visible light. The dual mode ratiometric response of Hg2+ can be ascribed to the rapid redox reaction between Hg2+ and Ag0 on the surface of AgNCs and the subsequent formation of silver amalgam. The resultant dual-mode ratiometric sensor has been successfully applied to the determination of Hg2+ in environmental water samples. This study provides a new strategy to synthesize dual-emission AgNCs by scientifically designing terminus sequence of ssDNA template, and develops a facile and efficient single-probe and dual-mode ratiometric sensor for visual monitoring of Hg2+.