{"title":"Carbon nanotubes decorated with bimetallic PtCo nanoparticles for sensitive detection of uric acid","authors":"Shun Lu , Shouqin Xiang , Chuan Wang , Hong Liu","doi":"10.1016/j.elecom.2024.107774","DOIUrl":null,"url":null,"abstract":"<div><p>Common methods based on enzymatic approaches for uric acid (UA) have potential issues such as limited detection range, low linearity, and susceptibility to interference. Our study focuses on enhancing the sensitivity and selectivity of detecting UA by decorating carbon nanotubes (CNTs) with bimetallic platinum-cobalt nanoparticles (PtCo/CNTs) using an adsorbing-thermal reducing method for electrochemical analysis. Physical characterizations are employed to confirm its structural and element compositions. Then, an electrochemical biosensor based on screen printed electrode (SPE) modified with PtCo/CNTs was constructed for UA determination. PtCo/CNTs modified SPE (PtCo/CNTs@SPE) demonstrates significant electrochemical activity and selectivity toward UA detection due to the synergistic effect between PtCo nanoparticles and CNTs, and the excellent electrical conductivity. Under optimized conditions, the current response of UA at the PtCo/CNTs@SPE presented linear dependence on the concentration, ranging from 0.1 µM to 3000.0 µM with a low limit of detection of 0.05 µM. In addition, the selectivity, stability, and practical applications of the as-prepared sensor are also explored.</p></div>","PeriodicalId":304,"journal":{"name":"Electrochemistry Communications","volume":"166 ","pages":"Article 107774"},"PeriodicalIF":4.7000,"publicationDate":"2024-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1388248124001176/pdfft?md5=7245ae6927817956c71a5b9a4bae2878&pid=1-s2.0-S1388248124001176-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochemistry Communications","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1388248124001176","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Common methods based on enzymatic approaches for uric acid (UA) have potential issues such as limited detection range, low linearity, and susceptibility to interference. Our study focuses on enhancing the sensitivity and selectivity of detecting UA by decorating carbon nanotubes (CNTs) with bimetallic platinum-cobalt nanoparticles (PtCo/CNTs) using an adsorbing-thermal reducing method for electrochemical analysis. Physical characterizations are employed to confirm its structural and element compositions. Then, an electrochemical biosensor based on screen printed electrode (SPE) modified with PtCo/CNTs was constructed for UA determination. PtCo/CNTs modified SPE (PtCo/CNTs@SPE) demonstrates significant electrochemical activity and selectivity toward UA detection due to the synergistic effect between PtCo nanoparticles and CNTs, and the excellent electrical conductivity. Under optimized conditions, the current response of UA at the PtCo/CNTs@SPE presented linear dependence on the concentration, ranging from 0.1 µM to 3000.0 µM with a low limit of detection of 0.05 µM. In addition, the selectivity, stability, and practical applications of the as-prepared sensor are also explored.
期刊介绍:
Electrochemistry Communications is an open access journal providing fast dissemination of short communications, full communications and mini reviews covering the whole field of electrochemistry which merit urgent publication. Short communications are limited to a maximum of 20,000 characters (including spaces) while full communications and mini reviews are limited to 25,000 characters (including spaces). Supplementary information is permitted for full communications and mini reviews but not for short communications. We aim to be the fastest journal in electrochemistry for these types of papers.