Abstract
We report on a hybrid bioelectrochemical system that integrates an energy converting part, viz. a glucose/oxygen enzymatic fuel cell, with a charge-storing component, in which the redox features of the immobilized redox protein cytochrome c (cyt c) were utilized. Bilirubin oxidase and pyrroloquinoline quinone-dependent glucose dehydrogenase (PQQ-GDH) were employed as the biocatalysts for dioxygen reduction and glucose oxidation, respectively. A bi-protein PQQ-GDH/cyt c signal chain was created that facilitates electron transfer between the enzyme and the electrode surface. The assembled supercapacitor/biofuel cell hybrid biodevice displays a 15 times higher power density tested in the pulse mode compared to the performance achieved from the continuously operating regime (4.5 and 0.3 μW cm−2, respectively) with an 80% residual activity after 50 charge/discharge pulses. This can be considered as a notable step forward in the field of glucose/oxygen membrane-free, biocompatible hybrid power sources.
| Original language | English |
|---|---|
| Journal | Bioelectrochemistry |
| Volume | 128 |
| Pages (from-to) | 94-99 |
| Number of pages | 6 |
| ISSN | 1567-5394 |
| DOIs | |
| Publication status | Published - 2019 |
Keywords
- Enzymatic fuel cell
- Bilirubin oxidase
- Glucose dehydrogenase
- Cytochrome c
- Hybrid bioelectrochemical system