Controllable graphene oxide mediated efficient electron transfer pathways across self-assembly monolayers: A new class of graphene based electrodes

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• 作者：Na Kong^a ; Mahesh Vaka^a ; Nguyen Dang Nam^c ; Colin J. Barrow^a ; Jingquan Liu^b ; Xavier A. Conlan^a ; ^{xavier.conlan@deakin.edu.au" class="auth_mail" title="E-mail the corresponding author} ; Wenrong Yang^a ; ^{wenrong.yang@deakin.edu.au" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Chemical Reduced Graphene Oxide ; Electron Transfer ; Self-Assembled Monolayer
• 刊名：Electrochimica Acta
• 出版年：2016
• 出版时间：20 August 2016
• 年：2016
• 卷：210
• 期：Complete
• 页码：539-547
• 全文大小：2842 K

文摘

In this paper, the influence of chemically reduced graphene oxide sheets (CRGOs) on the electrochemical performance through methyl or carboxylic acid terminated self-assembled monolayers (SAMs) is reported. The gold electrode was initially modified with methyl or carboxylic acid terminated alkanethiols with various carbon chain lengths (n = 4, 6, 8 and 11) and subsequently immobilization of the CRGOs on a SAM surface was achieved via a hydrophobic and electrostatic interaction. By using the potassium ferricyanide as a redox probe, it was observed that CRGOs could effectively enhance the heterogeneous electron transfer (ET) of the SAM due to a tunneling effect. The assemblies based on thiol end groups with methyl head groups were observed to afford more hydrophobic interaction binding with CRGOs with a higher reduction time than the assemblies developed with thiol end groups and a −COOH group which were shown to bind more electrostatically with CRGOs, a lowering reduction time. The Nyquist plots developed show a gradual decrease of the charge transfer resistance (R_ct) of [Fe(CN)₆]^3−/4− redox couple at the CRGOs-SAMs electrode with the controllable adsorption of different CRGO’s onto the SAM. Depending on the chain length and terminal functional group the electron transfer rate kinetics were observed to differ considerably.