• 文献标题:   The effect of N-configurations on selective detection of dopamine in the presence of uric and ascorbic acids using surfactant-free N-graphene modified ITO electrodes
  • 文献类型:   Article
  • 作  者:   MATSOSO BJ, MUTUMA BK, BILLING C, RANGANATHAN K, LEROTHOLI T, JONES G, COVILLE NJ
  • 作者关键词:   ndoped graphene, dopamine, nconfiguration, ito electrode, chemical vapour deposition
  • 出版物名称:   ELECTROCHIMICA ACTA
  • ISSN:   0013-4686 EI 1873-3859
  • 通讯作者地址:   Univ Witwatersrand
  • 被引频次:   9
  • DOI:   10.1016/j.electacta.2018.08.017
  • 出版年:   2018

▎ 摘  要

Nitrogen doped graphene based electrodes are increasingly gaining attention for application in voltammetric detection of dopamine (DA). However, little attention has been paid on the influence of the relative concentration of N-configurations on the electrocatalytic performance of these electrodes. Therefore in this study, sensitive and selective surfactant-free indium tin oxide (ITO) electrodes, modified with N-graphene films of varying nitrogen configurations, were employed for detection of DA in the presence of uric (UA) and ascorbic acids (AA). The N-graphene films, initially characterized using XPS, consisted of 38-60% pyridinic-N, 4-31% pyrrolic-N, 13-56% graphitic-N, and 2-9% oxidized pyridinic-N (NOx). The results showed that the NGr/ITO electrodes exhibited excellent selective electrocatalytic performance for the oxidation of DA in the presence of UA and AA. As a result, the detection limits (S/N = 3) of DA were determined to be 0.131 +/- 0.005 mu M, 0.153 +/- 0.03 mu M, and 0.645 +/- 0.07 mu M at the NGr-2/ITO, NGr-10/ITO and NGr-20/ITO electrodes, respectively. The excellent electrocatalytic activity of NGr-2/ITO electrode towards the oxidation of DA was ascribed mainly to an improved pi-pi interaction of the NOx (9.2%) and pyrrolic N-configurations (59.6%) with the hydroxyl and amine groups on DA. Generally, this study has provided a procedure for designing new surfactant-free 2D N-graphene based electrochemical sensors with specific electrocatalytic performance. (C) 2018 Elsevier Ltd. All rights reserved.