Abstract
Open-cell nanoporous Au (np-Au) electrodes with pore size of approximately 40 nm were fabricated by dealloying of Au-Ag, and surfaces of the electrodes were modified with a self-assembled monolayer (SAM) of 4- aminothiophenol to enhance the electrocatalytic activities of immobilized laccase and glucose oxidase. Enzymeimmobilized SAM-modified np-Au working electrodes exhibited additional reduction-oxidation peak pairs in cyclic voltammograms in buffer solution (pH05.0). Thus, the SAM on the np-Au facilitated electron transfer between the electrode and reactants. First-principles calculations of perfect and defective Au (111) surfaces indicated that the atomic defects at nanoligament surface of np-Au are critically responsible for the electron transfer enhancement. For the utilization of these results, a glucose/O 2 biofuel cell composed of these enzymeimmobilized SAM-modified np-Au electrodes was preliminarily fabricated, and it exhibited a maximumpower density of 52 μW/cm 2 at 20°C. Further optimization of nanoporous structures and kinds of SAM will improve the performance of biofuel cells.© 2011 The Author(s).
Author supplied keywords
Cite
CITATION STYLE
Hakamada, M., Takahashi, M., & Mabuchi, M. (2012). Enzyme electrodes stabilized by monolayer-modified nanoporous Au for biofuel cells. Gold Bulletin, 45(1), 9–15. https://doi.org/10.1007/s13404-011-0038-1
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.