Herein a system capable of simultaneously sensing glucose and harnessing sufficient energy to power a digital device is presented. This system is powered by an enzymatic glucose biofuel cell consisting of pyroloquinoline quinone glucose dehydrogenase‐modified bioanode and bilirubin oxidase‐modified biocathode. The electrical parameters from a single biofuel cell were amplified to 1.4 V using a charge pump circuit consisting of a capacitive element that senses glucose. Furthermore, a steady output DC supply of 3.2 V was obtained by interfacing a step‐up DC convertor circuit to the charge pump circuit. Such a system simultaneously senses glucose and harnesses energy in the presence of various glucose concentrations. The self‐powered glucose biosensor exhibited an improved sensitivity of 86.42 Hz/cm2mM with a linear range extending to 20 mM when operating a digital device simultaneously. This is a 3.7‐fold increase in sensor sensitivity when compared with previous self‐powered glucose biosensors. This novel self‐powered glucose biosensing system shows a promising future for powering implantable devices and assessing patient health.
A hybrid biofuel cell (HBFC) is explored as a low-cost alternative to abiotic and enzymatic biofuel cells. Here the HBFC provides an enzymeless approach for the fabrication of the anodic electrode while employing an enzymatic approach for the fabrication of the cathodic electrode to develop energy harvesting platform to power bioelectronic devices. The anode employed 250 μm braided gold wire modified with colloidal platinum (Au-co-Pt) and bilirubin oxidase (BODx) modified gold coated Buckypaper (BP-Au-BODx) cathode. The functionalization of the gold coated multi-walled carbon nanotube (MWCNT) structures of the BP electrodes is achieved by 3-mercaptopropionic acid surface modification to possess negatively charged carboxylic groups and subsequently followed by EDC/Sulfo-NHS (1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and N-Hydroxysulfosuccinimide) crosslinking with BODx. The integration of the BODx and gold coated MWCNTs is evaluated for bioelectrocatalytic activity. The Au-co-Pt and BP-Au-BODx exhibited excellent electrocatalytic activity towards glucose oxidation with a linear dynamic range up to 20 mM glucose and molecular oxygen reduction, respectively. The HBFC demonstrated excellent performance with the largest open circuit voltages of 0.735 V and power density of 46.31 μW/cm2in 3 mM glucose. In addition, the HBFC operating on 3 mM glucose exhibited excellent uninterrupted operational stability while continuously powering a small electronic device. These results provide great opportunities for implementing this simple but efficient HBFC to harvest the biochemical energy of target fuel(s) in diverse medical and environmental applications.
more » « less- PAR ID:
- 10153319
- Publisher / Repository:
- Nature Publishing Group
- Date Published:
- Journal Name:
- Scientific Reports
- Volume:
- 8
- Issue:
- 1
- ISSN:
- 2045-2322
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
more » « less
-
A glucose biofuel cell on a flexible bacterial nanocellulose film was prepared. The bioelectrodes were printed using gold ink as the conductive material. The anode was modified with colloidal platinum for the oxidation of glucose. The cathode was modified with a nanocomposite comprising gold nanoparticles (AuNPs) and silver oxide (Ag2O) nanoparticles. The cathode was characterized via cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and UV spectroscopy techniques. The assembled biofuel cell generated a maximum open circuit voltage (V oc ) of 0.485 V, short circuit current (I sc ) of 0.352 mA/cm 2 , and a maximum peak power density (P max ) of 0.032 mW/cm 2 when operating in 30 mM concentration. This system showed a stable and linear performance with a linear range of 1 mM to 30 mM glucose. The gold printed electrode process is applicable to the development of wearable and implantable abiotic biofuel cell.more » « less
-
A glucose biofuel cell is presented using laser induced 3D graphene (LIG) substrate integrated with catalytic active nanomaterials for harnessing the biochemical energy of glucose. The LIG anode comprised glucose dehydrogenase immobilized on reduced graphene oxide and multiwalled carbon nanotubes (RGO/MWCNTs) nanocomposite for glucose oxidation. The LIG cathode is modified with RGO/MWCNTs and silver oxide (Ag 2 O) nanocomposites for the reduction of oxygen. The assembled biofuel cell exhibited a linear peak power response up to 18 mM glucose with sensitivity of 0.63 μW mM -1 cm −2 and exhibited good linearity (r 2 = 0.99). The glucose biofuel cell showed an open-circuit voltage of 0.365 V, a maximum power density of 11.3 μW cm −2 at a cell voltage of 0.25 V, and a short-circuit current density of 45.18 μA cm −2 when operating in 18 mM glucose. Cyclic voltammetry revealed the bioanode exhibited similar linearity for the detection of glucose. These results demonstrate that LIG based bioelectrodes offer great promise for diverse applications in the development of hybrid biofuel cell and biosensor technology.more » « less
-
Uniform and porous CoNi 2 Se 4 was successfully synthesized by electrodeposition onto a composite electrode comprising reduced graphene oxide (rGO) anchored on a Ni foam substrate (prepared hydrothermally). This CoNi 2 Se 4 –rGO@NF composite electrode has been employed as an electrocatalyst for the direct oxidation of glucose, thereby acting as a high-performance non-enzymatic glucose sensor. Direct electrochemical measurement with the as-prepared electrode in 0.1 M NaOH revealed that the CoNi 2 Se 4 –rGO nanocomposite has excellent electrocatalytic activity towards glucose oxidation in an alkaline medium with a sensitivity of 18.89 mA mM −1 cm −2 and a wide linear response from 1 μM to 4.0 mM at a low applied potential of +0.35 V vs. Ag|AgCl. This study also highlights the effect of decreasing the anion electronegativity on enhancing the electrocatalytic efficiency by lowering the potential needed for glucose oxidation. The catalyst composite also exhibits high selectivity towards glucose oxidation in the presence of several interferents normally found in physiological blood samples. A low glucose detection limit of 0.65 μM and long-term stability along with a short response time of approximately 4 seconds highlights the promising performance of the CoNi 2 Se 4 –rGO@NF electrode for non-enzymatic glucose sensing with high precision and reliability.more » « less
-
more » « less
Nanofiber technology is leading the revolution of wearable technology and provides a unique capability to fabricate smart textiles. With the novel fabrication technique of electrospinning, nanofibers can be fabricated and then manufactured into a durable conductive string for the application of smart textiles. This paper presents an electrospun nanofiber mesh-based (NF-Felt) string electrode with a conducting polymer coating for an electrochemical enzymatic glucose sensor. The surface area of a nanofiber matrix is a key physical property for enhanced glucose oxidase (GOx) enzyme binding for the development of an electrochemical biosensor. A morphological characterization of the NF-Felt string electrode was performed using scanning electron microscopy (SEM) and compared with a commercially available cotton–polyester (Cot-Pol) string coated with the same conducting polymer. The results from stress–strain testing demonstrated high stretchability of the NF-Felt string. Also, the electrochemical characterization results showed that the NF-Felt string electrode was able to detect a glucose concentration in the range between 0.0 mM and 30.0 mM with a sensitivity of 37.4 μA/mM·g and a detection limit of 3.31 mM. Overall, with better electrochemical performance and incredible flexibility, the NF-Felt-based string electrode is potentially more suitable for designing wearable biosensors for the detection of glucose in sweat.
