{"title":"Efficacy of films of uncapped gold nanoparticle as electrodes for direct electron transfer to redox proteins","authors":"Kentaro Akiyama , Hirotaka Okabe , Taisei Motomura , Naoki Matsuda , Yasuhiro Mie","doi":"10.1016/j.elecom.2024.107695","DOIUrl":null,"url":null,"abstract":"<div><p>Electrochemical manipulation of enzymes is expected to enable the rapid detection of marker molecules and the efficient production of valuable materials. We have fabricated an Au nanoparticle (AuNP) thin film electrode in our previous study, which enables more enhanced heterogeneous electron transfer reactions than a conventional planner Au electrode. In this study, electrochemical evaluation of cytochrome <em>c</em> was performed using the AuNP thin film electrodes with and without self-assembled monolayer (SAM) modification to assess its practicality for protein electrochemistry. The 4-pyridinethiol- and 7-carboxy-1-heptanethiol-modified AuNP thin film electrodes showed much larger faradaic current values attributed to redox reactions compared to those of the Au electrodes. The results indicate that the nanostructural effects of the AuNP thin film electrode are beneficial. Importantly, even when the non-modified (bare) AuNP thin film electrode was applied, it exhibited the clear electrochemical response of cyt <em>c</em>, while the bare Au electrode showed no such a response. This study provides evidence that the AuNP thin film electrode functions as a potent bioelectrocatalysts due to the nanostructure-specific properties.</p></div>","PeriodicalId":304,"journal":{"name":"Electrochemistry Communications","volume":"161 ","pages":"Article 107695"},"PeriodicalIF":4.7000,"publicationDate":"2024-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1388248124000389/pdfft?md5=f55da446d307c81f2afb67c2d4d39f8b&pid=1-s2.0-S1388248124000389-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochemistry Communications","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1388248124000389","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
Electrochemical manipulation of enzymes is expected to enable the rapid detection of marker molecules and the efficient production of valuable materials. We have fabricated an Au nanoparticle (AuNP) thin film electrode in our previous study, which enables more enhanced heterogeneous electron transfer reactions than a conventional planner Au electrode. In this study, electrochemical evaluation of cytochrome c was performed using the AuNP thin film electrodes with and without self-assembled monolayer (SAM) modification to assess its practicality for protein electrochemistry. The 4-pyridinethiol- and 7-carboxy-1-heptanethiol-modified AuNP thin film electrodes showed much larger faradaic current values attributed to redox reactions compared to those of the Au electrodes. The results indicate that the nanostructural effects of the AuNP thin film electrode are beneficial. Importantly, even when the non-modified (bare) AuNP thin film electrode was applied, it exhibited the clear electrochemical response of cyt c, while the bare Au electrode showed no such a response. This study provides evidence that the AuNP thin film electrode functions as a potent bioelectrocatalysts due to the nanostructure-specific properties.
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.