Biofuel cells based on direct enzyme–electrode contacts using PQQ-dependent glucose dehydrogenase/bilirubin oxidase and modified carbon nanotube materials
By Scherbahn, V.; Putze, M.T.; Dietzel, B.; Heinlein, T.; Schneider, J.J. & Lisdat, F.
Published in Biosensors and Bioelectronics
NULL
2014
Abstract
Two types of carbon nanotube electrodes (1) buckypaper (BP) and (2) vertically aligned carbon nanotubes (vaCNT) have been used for elaboration of glucose/O2 enzymatic fuel cells exploiting direct electron transfer. For the anode pyrroloquinoline quinone dependent glucose dehydrogenase ((PQQ)GDH) has been immobilized on [poly(3-aminobenzoic acid-co-2-methoxyaniline-5-sulfonic acid), PABMSA]-modified electrodes. For the cathode bilirubin oxidase (BOD) has been immobilized on PQQ-modified electrodes. PABMSA and PQQ act as promoter for enzyme bioelectrocatalysis. The voltammetric characterization of each electrode shows current densities in the range of 0.7–1.3 mA/cm2. The BP-based fuel cell exhibits maximal power density of about 107 µW/cm2 (at 490 mV). The vaCNT-based fuel cell achieves a maximal power density of 122 µW/cm2 (at 540 mV). Even after three days and several runs of load a power density over 110 µW/cm2 is retained with the second system (10 mM glucose). Due to a better power exhibition and an enhanced stability of the vaCNT-based fuel cells they have been studied in human serum samples and a maximal power density of 41 µW/cm2 (390 mV) can be achieved.
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