A single-liquid miniature biofuel cell with boosting power density via gas diffusion bioelectrodes. Issue 16 (13th December 2019)

• Record Type: Journal Article
• Authors: Wan, Jing; Mi, Li; Tian, Zhaoyan; Li, Quan; Liu, Songqin
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 16(2020)
• Page Start: 3550
• Page End: 3556
• Publication Date: 2019-12-13
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Biomedical materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c9tb02100k
• Languages: English
• ISSNs: 2050-750X

Abstract

Abstract : A single-liquid glucose–O2 cell is constructed by gas diffusion electrode. O2 diffusion directly from air to active sites of enzyme enhances the enzymatic reaction rate. The maximum power output density of the cell is 53 μW cm −2 . Abstract : The low solubility of gas molecules in aqueous solutions has limited the power density output of enzymatic biofuel cells. Herein, a single-liquid miniature glucose–O2 fuel cell was constructed by using gas diffusion electrodes, which were prepared by immobilizing glucose oxidase (GOx) or laccase (Lac) modified on a porous structured carbon paper (CP). Due to the fast and direct O2 diffusion from air to the active sites of the immobilized enzyme through the pores of the CP anode/cathode with controlled wettability, the maximum power output densities dramatically increased to 9.64 μW cm −2 at 0.43 V and 53.0 μW cm −2 at 0.45 V for the cell in 5 mM glucose and after exposing the cell to air or O2 atmosphere, respectively. Interestingly, the resulting single-liquid cell could harvest power from human serum operating at a maximum power density of 49.0 μW cm −2 at 0.2 V. The biofuel cell fabricated by the gas diffusion electrodes displayed advantages such as high output power density, low cost and high 'on-chip' integrability and miniaturization, which suggest its great potential for implantable self-powered sensors and for many future applications.