Defect-Enriched Graphene Nanoribbons Tune the Adsorption Behavior of the Mediator to Boost the Lactate/Oxygen Biofuel Cell.

Owing to the high efficiency and specificity in moderate conditions, enzymatic biofuel cells (EBFCs) have gained significant interest as a promising energy source for wearable devices. However, the instability of the bioelectrode and the lack of efficient electrical communication between the enzymes and electrodes are the main obstacles. Herein, defect-enriched 3D graphene nanoribbons (GNRs) frameworks are fabricated by unzipping multiwall carbon nanotubes, followed by thermal annealing. It is found that defective carbon shows stronger adsorption energy towards the polar mediators than the pristine carbon, which is beneficial to improving the stability of the bioelectrodes. Consequently, the EBFCs equipped with the GNRs exhibit a significantly enhanced bioelectrocatalytic performance and operational stability, delivering an open-circuit voltage and power density of 0.62 V, 70.7 µW/cm2, and 0.58 V, 18.6 µW/cm2 in phosphate buffer solution and artificial tear, respectively, which represent the high levels among the reported literature. This work provides a design principle according to which defective carbon materials could be more suitable for the immobilization of biocatalytic components in the application of EBFCs.

Carbon nanorods assembled coral-like hierarchical meso-macroporous carbon as sustainable materials for efficient biosensing and biofuel cell.

Sustainable conversion of renewable biomass into high-performance electrode materials has attracted extensive scientific and technological attention. However, to our knowledge, the potential of biomass derived carbon in biosensors and biofuel cells (BFCs) developments remains to be explored. Herein, the carbon nanorods assembled coral-like hierarchical meso-macroporous carbon (CN-CHMC) was synthesized as a sustainable electrode material to construct biosensor and lactate/air BFC. The CN-CHMC from cucumber (Cucumis sativus) possesses porous structure and plentiful defects, which not only facilitate the effective immobilization of enzymes but also accelerate electron transfer on the bioelectrode surfaces. As an electrochemical lactate biosensor, the CN-CHMC-based biosensor exhibits a wider linear range with lower detection limit (3.6 µM) and higher sensitivities (57.18 and 30.99 µA mM-1 cm-2) compared to carbon nanotube (CNT)-based biosensor. The feasibility of CN-CHMC-based biosensor in practical analysis is demonstrated by detecting lactate contents in real samples. By coupling with bilirubin oxidase-based biocathode, the lactate/air BFC equipped with CN-CHMC reveals a higher output power (112.7 µW cm-2) than that of CNT-based BFC. More interestingly, the lactate/air BFC demonstrates the ability to harvest energy from multi-component samples. The application of CN-CHMC may provide a new avenue to synthesize electrode materials with economical cost and excellent electrochemical activity.

Hybrid catalyst cascade for enhanced oxidation of glucose in glucose/air biofuel cell.

Redox enzymes are capable of harvesting electrical energy from biofuels in high catalytic activity and under mild condition. However, it is difficult to achieve efficient electron transfer and deep oxidation of biofuels simultaneously in a single-enzyme catalytic system. Herein, we report a hybrid catalyst cascade consisting of an organic oxidation catalyst, 2,2,6,6-tetramethyl-1-piperidine N-oxyl (TEMPO), and an enzyme, glucose oxidase (GOx), for electrochemical oxidation of glucose. It is found that TEMPO is capable of mediating electron transfer between the redox center of GOx and the electrode surface. While glucose can be oxidized into glucuronic acid under neutral conditions. Thus, combining GOx and TEMPO, we are able to achieve 4e- electrooxidation of glucose using the hybrid enzymatic and organic cascade (HEOC) system. When coupled with an air-breathing Pt cathode, the resulting glucose/air biofuel cell using the proposed HEOC anode exhibits a maximum power density of 38.1 µW cm-2 with a short-circuit current of 651.4 µA cm-2, which can be attributed to the enhanced energetic efficiency, enabling TEMPO a promising catalyst for glucose oxidation in bioelectronics applications.

Biomass derived worm-like nitrogen-doped-carbon framework for trace determination of toxic heavy metal lead (II).

The worm-like nitrogen-doped-carbon framework (WNCF) with abundant edge-plane-like defective sites (EDSs) was synthesized by using natural wax gourd (Benincasa hispida) as the main carbon precursor and milk yielded by Chinese Holstein cattle (Holstein Friesian) as the nitrogen precursor for the first time. The Nafion-dispersed WNCF (Nafion-WNCF) was employed to design a highly sensitive electrochemical sensor for the trace determination of toxic heavy metal lead (II) (Pb2+) by the differential pulse anodic stripping voltammetry (DPASV). Some key experimental factors including calcination temperature of WNCF, pH value of the buffer solution, deposition potential, deposition time and the concentration of bismuth (Bi3+) were optimized for the stripping analysis of Pb2+. Under the optimum experimental condition, Nafion-WNCF modified bismuth film glassy carbon electrode (Nafion-WNCF/BFGCE) exhibits a wide linear range from 0.5 µg L-1 to 100 µg L-1 and a low detection limit of 0.2 µg L-1 (S/N = 3) for detecting Pb2+. Especially, Nafion-WNCF/BFGCE was successfully applied to determine Pb2+ in tap water and lake water samples. All the results suggest that the WNCF can be considered as a green and low-cost nanomaterial for the precision detection of Pb2+ in real samples.

Correction to: Synthesis of a three-dimensional interconnected carbon nanorod aerogel from wax gourd for amperometric sensing.

The published version of this article, unfortunately, contains error. The authors regret that one typo was present in the first author name "Cuxing Xu" when it should be "Cuixing Xu".

Electrochemical sensing platform based on kelp-derived hierarchical meso-macroporous carbons.

In this paper, kelp (Laminaria japonica), as a kind of abundant biomass, is used as the precursor for the preparation of kelp-derived hierarchical meso-macroporous carbons (K-dHMMCs) through the carbonization under nitrogen (N2) atmosphere at high temperature. The K-dHMMCs exhibits the unique structure with high specific surface area of 416.02 m2 g-1, large pore volume of 0.24 cm3 g-1, the hierarchical meso-macroporous size distribution centered at 2, 12 and 82 nm and high density of defective sites, enabling K-dHMMCs attractive for the electrocatalysis. Drop-casting K-dHMMCs on the glassy carbon (GC) surface allows the construction of K-dHMMCs based electrochemical sensing platform, which shows electrocatalytic activities towards many electroactive molecules, such as potassium ferricyanide, nicotinamide adenine dinucleotide (NADH), hydrogen peroxide (H2O2), dopamine (DA), uric acid (UA), ascorbic acid (AA), epinephrine (EP), l-tyrosine (Tyr) and acetaminophen (APAP). Especially, the K-dHMMCs modified GC (K-dHMMCs/GC) electrode exhibits higher sensitivity, wider linear range, and lower detection limit than both carbon nanotubes modified GC (CNTs/GC) and GC electrodes for H2O2 detection, which makes the K-dHMMCs/GC electrode to be able to determine the H2O2 levels in human urine sample and monitor the H2O2 released from human cancer cells. These results demonstrate that K-dHMMCs/GC possesses a great potential for conventional electrochemical sensing applications.