{"title":"基于 AgCuO/Cu2O 纳米酶的比色法和光电化学双模型策略用于检测血清中的 Hg2+","authors":"Xinxin Gu, Tao Cheng, Tairu Yin, Xiaoyu Guo, Xinling Liu, Ying Wen, Haifeng Yang, Yiping Wu","doi":"10.1149/1945-7111/ad586d","DOIUrl":null,"url":null,"abstract":"\n A stable and highly visible-light responsive semiconductor material of AgCuO/Cu2O was prepared to develop a colorimetric and photoelectrochemical (PEC) dual-sensing mode for broad-range Hg2+ detection. The AgCuO/Cu2O was evidenced with Hg2+-enhanced peroxidase activity. In the solution, the appearance of Hg2+ promotes AgCuO/Cu2O to catalyze more 3, 3′, 5, 5′-tetramethylbenzidine (TMB) oxidization, deepening the color of the TMB solution and increasing the light absorption, thus realizing the colorimetric detection of Hg2+. The linear response range is 1 nmol·L-1 to 10 μmol·L-1, and the detection limit is 3.5 nmol·L-1. On the electrode surface, the emergence of Hg2+ facilitates AgCuO/Cu2O to convert more 4-chloro-1-naphthol (4-CN) into insoluble precipitates benzo-4-chlorohexadienone (4-CD), depressing the PEC signal and realizing the PEC detection of Hg2+ with a linear response range of 10 pmol·L-1 to 10 μmol·L-1 and a detection limit of 8.7 pmol·L-1. The enhancement of the enzyme-mimicking activity of AgCuO/Cu2O by Hg2+ is closely related to the in-situ formation of the Ag-Hg amalgam. The colorimetric and the PEC sensing modal complement each other, significantly broadening the detection range of Hg2+ and ensuring the reliability and accuracy of the results. The work paves the way for sensitive, selective, and accurate determination of Hg2+ in serum samples.","PeriodicalId":509718,"journal":{"name":"Journal of The Electrochemical Society","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"AgCuO/Cu2O Nanozyme-Based Colorimetric and Photoelectrochemical Dual-Models Strategy for Sensing Hg2+ in Serum\",\"authors\":\"Xinxin Gu, Tao Cheng, Tairu Yin, Xiaoyu Guo, Xinling Liu, Ying Wen, Haifeng Yang, Yiping Wu\",\"doi\":\"10.1149/1945-7111/ad586d\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n A stable and highly visible-light responsive semiconductor material of AgCuO/Cu2O was prepared to develop a colorimetric and photoelectrochemical (PEC) dual-sensing mode for broad-range Hg2+ detection. The AgCuO/Cu2O was evidenced with Hg2+-enhanced peroxidase activity. In the solution, the appearance of Hg2+ promotes AgCuO/Cu2O to catalyze more 3, 3′, 5, 5′-tetramethylbenzidine (TMB) oxidization, deepening the color of the TMB solution and increasing the light absorption, thus realizing the colorimetric detection of Hg2+. The linear response range is 1 nmol·L-1 to 10 μmol·L-1, and the detection limit is 3.5 nmol·L-1. On the electrode surface, the emergence of Hg2+ facilitates AgCuO/Cu2O to convert more 4-chloro-1-naphthol (4-CN) into insoluble precipitates benzo-4-chlorohexadienone (4-CD), depressing the PEC signal and realizing the PEC detection of Hg2+ with a linear response range of 10 pmol·L-1 to 10 μmol·L-1 and a detection limit of 8.7 pmol·L-1. The enhancement of the enzyme-mimicking activity of AgCuO/Cu2O by Hg2+ is closely related to the in-situ formation of the Ag-Hg amalgam. The colorimetric and the PEC sensing modal complement each other, significantly broadening the detection range of Hg2+ and ensuring the reliability and accuracy of the results. The work paves the way for sensitive, selective, and accurate determination of Hg2+ in serum samples.\",\"PeriodicalId\":509718,\"journal\":{\"name\":\"Journal of The Electrochemical Society\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Electrochemical Society\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1149/1945-7111/ad586d\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Electrochemical Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1149/1945-7111/ad586d","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
AgCuO/Cu2O Nanozyme-Based Colorimetric and Photoelectrochemical Dual-Models Strategy for Sensing Hg2+ in Serum
A stable and highly visible-light responsive semiconductor material of AgCuO/Cu2O was prepared to develop a colorimetric and photoelectrochemical (PEC) dual-sensing mode for broad-range Hg2+ detection. The AgCuO/Cu2O was evidenced with Hg2+-enhanced peroxidase activity. In the solution, the appearance of Hg2+ promotes AgCuO/Cu2O to catalyze more 3, 3′, 5, 5′-tetramethylbenzidine (TMB) oxidization, deepening the color of the TMB solution and increasing the light absorption, thus realizing the colorimetric detection of Hg2+. The linear response range is 1 nmol·L-1 to 10 μmol·L-1, and the detection limit is 3.5 nmol·L-1. On the electrode surface, the emergence of Hg2+ facilitates AgCuO/Cu2O to convert more 4-chloro-1-naphthol (4-CN) into insoluble precipitates benzo-4-chlorohexadienone (4-CD), depressing the PEC signal and realizing the PEC detection of Hg2+ with a linear response range of 10 pmol·L-1 to 10 μmol·L-1 and a detection limit of 8.7 pmol·L-1. The enhancement of the enzyme-mimicking activity of AgCuO/Cu2O by Hg2+ is closely related to the in-situ formation of the Ag-Hg amalgam. The colorimetric and the PEC sensing modal complement each other, significantly broadening the detection range of Hg2+ and ensuring the reliability and accuracy of the results. The work paves the way for sensitive, selective, and accurate determination of Hg2+ in serum samples.