Freestanding HRP-GOx redox buckypaper as an oxygen-reducing biocathode for biofuel cell applications

Horseradish peroxidase (HRP) was immobilized on redox buckypapers followed by electropolymerization of pyrrole-modified concanavalin A enabling the subsequent additional immobilization of the glycoprotein glucose oxidase (GOx). Biocatalytic buckypapers were formed using pyrene-modified 2,2′-azino-bi...

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Bibliographic Details
Main Authors: Cosnier, Serge, Elouarzaki, Kamal, Bourourou, M., Holzinger, M., Le Goff, A., Marks, Robert S.
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2015
Subjects:
Online Access:https://hdl.handle.net/10356/104725
http://hdl.handle.net/10220/25847
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Institution: Nanyang Technological University
Language: English
Description
Summary:Horseradish peroxidase (HRP) was immobilized on redox buckypapers followed by electropolymerization of pyrrole-modified concanavalin A enabling the subsequent additional immobilization of the glycoprotein glucose oxidase (GOx). Biocatalytic buckypapers were formed using pyrene-modified 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) or bis-Pyr-ABTS, a redox mediator, as a cross-linker. ABTS-functionalized buckypaper enhances the electron transfer of the bioelectrocatalytic reduction of H2O2 by HRP. Since H2O2 is produced during glucose oxidation by GOx in the presence of oxygen, the bienzymatic GOx–HRP biocathode achieves the complete reduction of oxygen into water. A clearly improved performance of the biocathode was obtained by using an improved biocompatible immobilization strategy, enabling the prevention of enzyme loss while ensuring both diffusion of glucose and O2 and the local production of H2O2. These freestanding flexible oxygen-reducing biocathodes can operate under physiological conditions and show a high onset potential at 0.60 (±0.01) V. In the presence of glucose (5 mM), such biocathodes exhibit a stable current density output of 1.1 (±0.1) mA cm−2 at 0.1 V under continuous one-hour discharge. Furthermore, a marked increase in lifetime was observed, the biocathode displaying 64% of its initial electrocatalytic activity after 15 days.