Abstract

We report a simple, versatile, and rapid method for the fabrication of optically-transparent large-area carbon nanotube (CNT) films via flotation assembly. After solvent-induced assembly, floating films were transferred to a flat supporting substrate to form conductive and transparent CNT film electrodes. The resulting electrodes, with uniform 40 ± 20 nm multi-walled CNT (MWCNT) layers, were characterized by electrochemical and microscopy methods. The flotation method does not require specialized thin-film instrumentation and avoids the need for surfactants and pre-oxidized CNTs which can hamper electrochemical performance. A proof-of-concept nanostructured bioelectrode demonstrating high sensitivity for glucose was developed with an electropolymerized poly(pyrene-adamantane) layer for host–guest immobilization of active β-cyclodextrin tagged GOx enzymes. The polymer provides pyrene groups for cross-linking to CNTs and pendant adamantane groups for binding the β-cyclodextrin groups of the tagged enzyme. This demonstration offers a new approach for the preparation of stable and transparent CNT film electrodes with attractive electrochemical properties towards future photobio- and bio-electrochemical fuel cells, electrochemical sensors, and electroanalysis.

Highlights

  • The use of carbon nanotubes (CNTs) has garnered plenty of interest within the nanoscience community for interfacing soft biological systems due to their chemical stability, high electrical/thermal conductivity [1], appealing mechanical properties [2] and biocompatibility [3]

  • The high specific surface area [4] and unique geometry make multi-walled CNTs (MWCNTs) an ideal candidate for the construction of highly-porous three-dimensional electrodes, especially given the ability to attach a plethora of functionalities [5,6,7]

  • CNT films with sub-100 nm thicknesses can exhibit high optical transparency which could be exploited for light-driven photoelectrochemical devices [15,16]

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Summary

Introduction

The use of carbon nanotubes (CNTs) has garnered plenty of interest within the nanoscience community for interfacing soft biological systems due to their chemical stability, high electrical/thermal conductivity [1], appealing mechanical properties [2] and biocompatibility [3]. CNT electrodes can provide a powerful platform for the immobilization of enzymes with high biomolecular activities [8,9] and have consistently demonstrated excellent performance for the electrical wiring of enzymes via direct and mediated electron transfer processes [10,11]. Use of nanoscale thin films can enhance mass transport of substrates/products and facilitate fast electron transfer with immobilized enzymes, opening up the possibility to improve bioelectrode performance for biofuel cell and biosensor devices [10,13,14]. CNT films with sub-100 nm thicknesses can exhibit high optical transparency which could be exploited for light-driven photoelectrochemical devices [15,16]

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