A bimetallic PtAu-modified carbon fiber electrochemical sensor for simultaneous and highly sensitive detection of catechol and hydroquinone in environmental water.
{"title":"A bimetallic PtAu-modified carbon fiber electrochemical sensor for simultaneous and highly sensitive detection of catechol and hydroquinone in environmental water.","authors":"Qi Xiao, Jiawen Li, Mingli Yang, Huihao Li, Yi Fang, Shan Huang","doi":"10.1039/d4ay01296h","DOIUrl":null,"url":null,"abstract":"<p><p>In this study, we report the development of a novel electrochemical sensor capable of the simultaneous detection of catechol (CC) and hydroquinone (HQ) through differential pulse voltammetry. The sensor is constructed using carbon fiber (CF) that has been intricately modified with bimetallic PtAu nanoparticles. The fabrication process involves subjecting CF to ultrasound treatment in an acidic mixture, resulting in the formation of activated carbon fiber (ACF). This activation step not only enhances surface roughness but also facilitates subsequent modification, ensuring the stability of the material. Bimetallic PtAu nanoparticles are then uniformly deposited onto the ACF surface through co-deposition from a metal precursor solution. The modified ACF, adorned with bimetallic PtAu nanoparticles, exhibits excellent conductivity and efficiently catalyzes both CC and HQ in a 10 mM phosphate-buffered saline solution at pH 7.0, thereby enabling their simultaneous detection. Under optimized experimental conditions, this electrochemical sensor achieves impressive detection limits of 0.019 μM for CC and 0.28 μM for HQ within the same concentration range of 0.5-50 μM, respectively. The practicality of the sensor is further demonstrated through recovery experiments using real water samples. This electrochemical sensor, with its superior performance and versatility, shows great potential for applications in analytical chemistry and environmental monitoring.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4ay01296h","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, we report the development of a novel electrochemical sensor capable of the simultaneous detection of catechol (CC) and hydroquinone (HQ) through differential pulse voltammetry. The sensor is constructed using carbon fiber (CF) that has been intricately modified with bimetallic PtAu nanoparticles. The fabrication process involves subjecting CF to ultrasound treatment in an acidic mixture, resulting in the formation of activated carbon fiber (ACF). This activation step not only enhances surface roughness but also facilitates subsequent modification, ensuring the stability of the material. Bimetallic PtAu nanoparticles are then uniformly deposited onto the ACF surface through co-deposition from a metal precursor solution. The modified ACF, adorned with bimetallic PtAu nanoparticles, exhibits excellent conductivity and efficiently catalyzes both CC and HQ in a 10 mM phosphate-buffered saline solution at pH 7.0, thereby enabling their simultaneous detection. Under optimized experimental conditions, this electrochemical sensor achieves impressive detection limits of 0.019 μM for CC and 0.28 μM for HQ within the same concentration range of 0.5-50 μM, respectively. The practicality of the sensor is further demonstrated through recovery experiments using real water samples. This electrochemical sensor, with its superior performance and versatility, shows great potential for applications in analytical chemistry and environmental monitoring.