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Abstract

Bioelectronics, which integrates biological systems with electronic devices, holds immense potential for advancing medical diagnostics and therapies. Most of these devices currently rely on traditional batteries that cannot be miniaturised effectively without losing capacity. Glucose fuel cells (GFCs) are emerging as a promising technology to provide miniaturised and biocompatible power sources for bioelectronics. In this study, a non-enzymatic GFC on a printed circuit board (PCB) is designed, which implements a nanocomposite catalytic anode electrode. The electrode is fabricated using a rapid one-step method involving the simultaneous electropolymerisation of polyaniline and the in-situ formation and entrapment of platinum (Pt) nanoparticles within the polymer matrix onto a highly porous gold surface. Physicochemical characterizations of the resulting nanocomposite confirmed the preservation of the highly porous gold structure post-polyaniline polymerisation, with an increased pore depth and uniform dispersion of Pt nanoparticles. The glucose fuel cells, with the nanocomposite electrode as the anode, generate a maximum power density of 61.7 ± 1.3 μW cm−2 at a current density of 221 ± 3 μA cm−2 under a physiological concentration of glucose (6 mM) and at 37 °C. This power performance is maintained over three months of repetitive testing, showing the greatest stability so far reported for glucose fuel cells. Accordingly, this work advances research in glucose fuel cell technology, paving the way for their practical use in medical devices.
Original languageEnglish
Article number237815
JournalJournal of Power Sources
Volume654
Early online date4 Jul 2025
DOIs
Publication statusPublished - 30 Oct 2025

Data Availability Statement

Data will be made available on request.

Funding

The authors would like to thank: the UK Research and Innovation (UKRI) Engineering and Physical Sciences Research Council (EPSRC) Grant EP/V010859/1 for funding, Philip Fletcher and Diana Szeidler-Lednitzky from the Material and Chemical Characterisation Facility (MC2) at the University of Bath (doi.org/10.15125/mx6j-3r54) for their help and assistance with the FE-SEM, TEM and Raman spectroscopy. This work was supported by the Henry Royce Institute for Advanced Materials, funded through EPSRC grants EP/R00661X/1 and EP/R010145/1, and the authors wish to acknowledge Dr Winnie Zheng Huang, from Royce@Oxford Centre for Energy Materials Research, University of Oxford, and Dr James Fon, National Graphene Institute, Manchester University, for their help with XPS and XRD analyses, respectively.

FundersFunder number
University of Bath
National Graphene Institute
TEM
University of Manchester
University of Oxford
UK Research & Innovation
Engineering and Physical Sciences Research CouncilEP/V010859/1
Henry Royce InstituteEP/R00661X/1, EP/R010145/1

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

Keywords

  • Bioelectronics
  • Electrocatalyst
  • Glucose fuel cells
  • Highly porous gold
  • Platinum nanoparticles
  • Polyaniline

ASJC Scopus subject areas

  • Renewable Energy, Sustainability and the Environment
  • Energy Engineering and Power Technology
  • Physical and Theoretical Chemistry
  • Electrical and Electronic Engineering

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