Enzymatic biofuel cells (EBFCs) are promising renewable and implantable power sources. However, their power output is often limited by inefficient electron transfer between the enzyme molecules and the electrodes, hindered mass transport, low conductivity, and small active surface area of the electrodes. To tackle these issues, we herein demonstrated a novel EBFC equipped with enzyme-functional...

Polyaromatic hydrocarbons were electro-oxidized on CNT electrodes and studied towards their capacity to transfer electrons from the enzyme FAD-GDH electrode. A mixture of pyrene NHS gave high performing biocathodes.

Considering crucial problems that limit use of platinum-based fuel cells, i.e. cost and availability, poisoning by fuel impurities and low selectivity, we propose electrocatalysis by enzymes as a valuable alternative to noble metals. Hydrogenase electrodes in neutral media achieve hydrogen equilibrium potential (providing 100% energy conversion), and display high activity in H(2) electrooxidati...

Enzyme-based biofuel cells (EBFCs) are systems that use a variety of organic compounds to produce electricity through oxido-reductase enzymes, such as oxidase or dehydrogenase as biocatalysts immobilized on electrodes. In this study, a single-chamber EBFC consisting of carbon electrodes that operating at ambient temperature in phosphate buffer, pH 7 is reported. The EBFC anode was based on gluc...

Enzyme entrapped in an electrosynthesized polymer film on a high-surface-area electrode is shown to be an attractive platform for the important class of amperometric biosensors based on oxidases and electrooxidation of the H2O2 generated by enzyme-catalyzed oxidation of analyte. Two Pt electrode surface morphologies, Pt black (Pt-BLK) and Pt nanowire brush (Pt-NW) were electrodeposited from chl...

ABSTRACT In this study, we developed a novel device consisting of 32 row and 32 column electrodes on a single chip for highthroughput electrochemical detection. The row and column electrodes were orthogonally arranged and connected to interdigitated array (IDA) electrodes at individual crossing points to form 1024 (32 × 32) sensor points. Electrochemical responses from each of the 1024 sensors ...

Here we report on the optimisation of a reagentless enzyme sensor for the detection of azide based on the mediated reduction of O2 by a laccase enzyme co-immobilised in a redox hydrogel on electrode surfaces. The sensor response is shown to be influenced by the enzyme loading, the electrolyte pH and ionic strength. The response of the sensor is stable, decreasing by only 25% over a sixteen-hour...