Asghar Niyazi

Effective glucose monitoring is paramount for patients with diabetes to effectively manage their condition and prevent health complications. Electrochemical sensors for glucose monitoring have key advantages over other systems, including cost-effectiveness, miniaturisation and portability, enabling the design of compact and wearable devices. Typically, enzymes are used in these sensors, with the limitations of poor stability and high cost. In alternative, this study reports the development of a gold and platinum composite nanostructured electrode and its testing as an abiotic (enzyme-free) electrocatalyst for glucose oxidation. The electrode consists of a film of highly porous gold electrodeposited onto gold-plated electrodes on a printed circuit board (PCB), which is coated with polyaniline decorated with platinum nanoparticles. The resulting nanocomposite structure shows a sensitivity towards glucose as high as 95.12 ± 2.54 µA mM⁻¹ cm⁻², nearly twice that of the highly porous gold electrodes, and excellent stability in synthetic interstitial fluid over extended testing, thus demonstrating robustness. Accordingly, this study lays the groundwork for the next generation of durable, selective, and affordable abiotic glucose biosensors.

Implantable and wearable bioelectronic systems can enable tailored therapies for the effective management of long-term diseases, thus minimising the risk of associated complications. In this context, glucose fuel cells hold great promise as in- or on-body energy harvesters for ultra-low-power bioelectronics and as self-powered glucose sensors. We report here the generation of gold nanostructures through a gold electrodeposition method in a soft template for the abiotic electrocatalysis of glucose in glucose fuel cells. Two different types of soft template were used: a lipid cubic phase-based soft template composed of Phytantriol and Brij^®-56, and an emulsion-based soft template composed of hexane and sodium dodecyl sulphate (SDS). The resulting gold structures were first characterised by SAXS, SEM and TEM to elucidate their structure, and then their electrocatalytic activity towards glucose was compared in both a three-electrode set-up and in a fuel cell set-up. The Phytantriol/Brij^®-56 template led to a nanofeather-like Au structure, while the hexane/SDS template led to a nanocoral-like Au structure. These templated electrodes exhibited similar electrochemical active surface areas (0.446 cm² with a roughness factor (RF) of 14.2 for Phytantriol/Brij^®-56 templated nanostructures and 0.421 cm² with an RF of 13.4 for hexane/SDS templated nanostructures), and a sensitivity towards glucose of over 7 μA mM⁻¹ cm⁻². When tested as the anode of an abiotic glucose fuel cell (in a phosphate-buffered solution with a glucose concentration of 6 mM), a maximum power density of 7 μW cm⁻² was reached; however the current density in the case of the fuel cell with the Phytantriol/Brij^®-56 templated anode was approximately two times higher, reaching the value of 70 μA cm⁻². Overall, this study demonstrates two simple, cost-effective and efficient strategies to manipulate the morphology of gold nanostructures, and thus their catalytic property, paving the way for the successful manufacturing of functional abiotic glucose fuel cells.