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1. Fabrication of highly effective hybrid biofuel cell based on integral colloidal platinum and bilirubin oxidase on gold support

   https://doi.org/10.1038/s41598-018-34740-w  

   Hasan, Md Qumrul ; Kuis, Robinson ; Narayanan, J. Shankara ; Slaughter, Gymama ( November 2018 , Scientific Reports)

   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 greatmore »opportunities for implementing this simple but efficient HBFC to harvest the biochemical energy of target fuel(s) in diverse medical and environmental applications.

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2. Gold and silver oxide conducting nanocomposite cathode for glucose biofuel cell

   https://doi.org/10.1109/SENSORS47087.2021.9639600  

   Banerjee, Saikat ; Nguyen, Mathew ; Slaughter, Gymama ( October 2021 , 2021 IEEE Sensors)

   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.
3. One-step hydrothermal synthesis of porous Ti ₃ C ₂ T _z MXene/rGO gels for supercapacitor applications

   https://doi.org/10.1039/D1NR02114A  

   Saha, Sanjit ; Arole, Kailash ; Radovic, Miladin ; Lutkenhaus, Jodie L. ; Green, Micah J. ( October 2021 , Nanoscale)

   Titanium carbide/reduced graphene oxide (Ti 3 C 2 T z /rGO) gels were prepared by a one-step hydrothermal process. The gels show a highly porous structure with a surface area of ∼224 m 2 g −1 and average pore diameter of ∼3.6 nm. The content of GO and Ti 3 C 2 T z nanosheets in the reaction precursor was varied to yield different microstructures. The supercapacitor performance of Ti 3 C 2 T z /rGO gels varied significantly with composition. Specific capacitance initially increased with increasing Ti 3 C 2 T z content, but at high Ti 3 C 2 T z content gels cannot be formed. Also, the retention of capacitance decreased with increasing Ti 3 C 2 T z content. Ti 3 C 2 T z /rGO gel electrodes exhibit enhanced supercapacitor properties with high potential window (1.5 V) and large specific capacitance (920 F g −1 ) in comparison to pure rGO and Ti 3 C 2 T z . The synergistic effect of EDLC from rGO and redox capacitance from Ti 3 C 2 T z was the reason for the enhanced supercapacitor performance. A symmetric two-electrode supercapacitor cell was constructed with Ti 3 Cmore »2 T z /rGO, which showed very high areal capacitance (158 mF cm −2 ), large energy density (∼31.5 μW h cm −2 corresponding to a power density of ∼370 μW cm −2 ), and long stability (∼93% retention) after 10 000 cycles.« less
4. A non-enzymatic glucose sensor based on a CoNi ₂ Se ₄ /rGO nanocomposite with ultrahigh sensitivity at low working potential

   https://doi.org/10.1039/c9tb00104b  

   Amin, Bahareh Golrokh ; Masud, Jahangir ; Nath, Manashi ( April 2019 , Journal of Materials Chemistry B)

   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-enzymaticmore »glucose sensing with high precision and reliability.« less
5. Laser-induced atmospheric Cu _x O formation on copper surface with enhanced electrochemical performance for non-enzymatic glucose sensing

   https://doi.org/10.1039/d1tc01289d  

   Sedaghat, Sotoudeh ; Nejati, Sina ; Bermejo, Luis Helena ; He, Zihao ; Alcaraz, Alejandro M. ; Roth, Alexander ; Li, Zheng ; Pol, Vilas G. ; Wang, Haiyan ; Rahimi, Rahim ( November 2021 , Journal of Materials Chemistry C)

   Copper oxide nanostructures are widely used for various applications due to their unique optical and electrical properties. In this work, we demonstrate an atmospheric laser-induced oxidation technique for the fabrication of highly electrochemically active copper oxide hierarchical micro/nano structures on copper surfaces to achieve highly sensitive non-enzymatic glucose sensing performance. The effect of laser processing power on the composition, crystallinity, microstructure, wettability, and color of the laser-induced oxide on copper (LIO-Cu) surface was systematically studied using scanning electron microscopy (SEM), grazing incidence X-ray diffraction (GI-XRD), Raman spectroscopy, energy dispersive X-ray spectroscopy (EDX), EDX-mapping, water contact angle measurements, and optical microscopy. Results of these investigations showed a remarkable increase in copper oxide composition by increasing the laser processing power. The pore size distribution and surface area of the pristine and LIO-Cu sample estimated by N 2 adsorption–desorption data showed a developed mesoporous LIO-Cu structure. The size of the generated nano-oxides, crystallinity, and electroactivity of the LIO-Cu were observed to be adjustable by the laser processing power. The electrocatalytic activity of LIO-Cu surfaces was studied by means of cyclic voltammetry (CV) within a potential window of −0.8 to +0.8 V and chronoamperometry in an applied optimized potential of +0.6 V, in 0.1more »M NaOH solution and phosphate buffer solution (PBS), respectively. LIO-Cu surfaces with optimized laser processing powers exhibited a sensitivity of 6950 μA mM −1 cm −2 within a wide linear range from 0.01 to 5 mM, with exceptional specificity and response time (<3 seconds). The sensors also showed excellent response stability over a course of 50 days that was originated from the binder-free robust electroactive film fabricated directly onto the copper surface. The demonstrated one-step LIO processing onto commercial metal films, can potentially be applied for tuneable and scalable roll-to-roll fabrication of a wide range of high surface area metal oxide micro/nano structures for non-enzymatic biosensing and electrochemical applications.« less