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Due to its sustainable approach, biomass is the subject of much research focused on the synthesis of multifunctional materials including electrodes for batteries and supercapacitors. In this work, sawdust from the processing of birch logs was used to produce a highly porous carbon material (CBW) that is employed for the construction of electrodes for aluminum batteries (ABs) and supercapacitors (SCs). A multitude of characterizations indicated that CBW is built in with highly disordered amorphous carbons and an extremely high specific surface area of 3029 m2 g−1 which is predominant with microporous features. The chemical analysis of CBW indicated the presence of a significant amount of oxygen functionalities. As a cathode of AB, CBW achieved discharge capacities 115, 74, 54, 50, 47, 43, and 29 mAh g−1 at current rates 0.1, 1.0, 2.0, 3.0, 4.0, 5.0, and 10.0 A g−1, respectively. Similarly, SC with CBW symmetric electrodes exhibited capacitances 143, 94, 87, 79, 74, 69, 65, and 51 F g−1 at current rates 0.1, 0.5, 1.0, 2.0, 3.0, 4.0, 5.0, and 10.0 A g−1, respectively. The electrochemical characterization revealed that CBW is promising for ABs and SCs, and controlling the porosity type could further enhance the performance.

The development of sustainable and efficient energy storage systems is crucial for addressing the growing global energy demand. This study investigates the potential of mesoporous carbon derived from lignin sulfonate as a cathode material for aluminium batteries. Lignin sulfonate, a by-product of the paper industry, was used as a precursor to synthesize mesoporous carbon through a facile and eco-friendly activation process. The resulting carbon material exhibited a high specific surface area of ∼ 2259 m2/g and a well-defined balance of micro- and meso- porosity, making it a promising cathode material for high-performance aluminium batteries. Electrochemical characterization showed that the mesoporous carbon cathode delivered an impressive specific capacity of 91 mAh/g at 1.0 A/g current density even after 7000 cycles with excellent cycling stability. It delivered superior rate capabilities of 105, 89, 80, 72, 67, 63, 90, and 105 mAh/g at 0.1, 1.0, 2.0, 3.0, 4.0, 5.0, 1.0, and 0.1 A/g current rates, respectively. The use of lignin-sulfonate as a precursor to prepare mesoporous carbon opens up a new sustainable way for improving the electrochemical performance of carbon-based cathode materials for aluminium batteries.

The development of biomass-based carbon materials has accelerated the research interest in environmental (e.g., adsorbents for wastewater decontamination) and energy applications (e.g., batteries). In this paper, we developed a series of carbon materials (CMs) using a sulfur doping strategy to improve the physicochemical, adsorptive and energy storage properties of the aforementioned CMs. CMs were prepared and optimized using an experimental design denoted as the Box-Behnken design approach with three independent factors (i.e., the temperature of pyrolysis, zinc chloride: biomass ratio and sulfur: biomass ratio), and the responses were evaluated, namely the Specific Surface Area (SBET), mesopore area (AMeso) and micropore area (AMicro) with the help of Nitrogen Physisorption. According to the statistical analysis, under the studied conditions, the responses were mainly influenced by the pyrolysis temperature and ZnCl2 ratio, while the sulfur content did not give rise to any remarkable differences in the selected responses. The physicochemical characterization of the CMs suggested that very high Specific Surface Areas ranging from 1069 to 1925 m2 g−1 were obtained. The sulfur doping resulted in up to 7.33wt.% of sulfur in the CM structure, which yielded CMs with more defects and hydrophilic surfaces. When tested as adsorbents, CMs exhibited a very high adsorption capacity (190 – 356mgg-1), and as anodes, they demonstrated a competitive Lithium Ion Battery (LIB) storage capacity, at least during the first five cycles (306 mAhg-1 at 1C for CM9). However, further studies on long-term cyclability are required to prove the CM materials suitability in LIBs. This work extends our understanding of how pyrolysis and sulfur doping of biomass feedstock affects carbon materials' usability, final characteristics and potential to use in wastewater decontamination by adsorption and as anodes in LIBs.

We have developed an Ir(PPy)3 photoredox-catalyzed cross-coupling reaction that allows installation of quinoxalinones at the C7 position of thiazolino ring-fused 2-pyridones (TRPs) under mild conditions. The methodology tolerates various substituted quinoxalinones and biologically relevant substituents on the C8 position of the TRP. The TRP scaffold has large potential in the development of lead compounds, and while the coupled products are interesting from a drug-development perspective, the methodology will be useful for developing more potent and drug-like TRP-based candidates.

Ensuring effective monitoring of methotrexate (MTX) levels in the bloodstream of cancer patients undergoing high-dose methotrexate chemotherapy is crucial to prevent potentially harmful side effects. However, the absence of portable analytical devices suitable for point-of-care bedside monitoring has presented a significant obstacle to achieving real-time MTX monitoring. In this study, we developed an impedimetric immunosensor that doesn't require reagents for measuring MTX levels in undiluted human blood serum. This reagentless approach simplifies the assay process, enabling rapid and straightforward MTX quantification. The immunosensor transducer was fabricated by electrodepositing conductive network of porous multiwalled carbon nanotube@polypyrrole/polytyramine on screen-printed gold microchip electrode (SP–Au/MWCNT70@PPy-PTA). Polyclonal anti-MTX antibodies were immobilized on the film, acting as the immunorecognition element. Non-specific binding was prevented by blocking the transducer interface with denatured bovine serum albumin (dBSA) fibrils, resulting in SP-Au/MWCNT70@PPy-PTA/anti-MTXAb|dBSA film electrode. When MTX binds to the SP-Au/MWCNT70@PPy-PTA/anti-MTXAb|dBSA interface, the film conductance and electron transfer resistance changes. This conductivity attenuation allows for electrochemical impedimetric signal transduction without a redox-probe solution. The electrochemical impedance spectroscopy (EIS) results showed increased charge transfer resistance and phase angle as MTX concentrations increased. The SP-Au/MWCNT70@PPy-PTA/anti-MTXAb|dBSA demonstrated high sensitivity, with a linear response from 0.02 to 20.0 μM and a detection limit of 1.93 nM. The detection limit was 50 times lower than the intended safe level of MTX in human serum. The immunosensor exhibited minimal cross-reactivity with endogenous MTX analogs and serum proteins. The SP-Au/MWCNT70@PPy-PTA/anti-MTXAb|dBSA immunosensor presents a simple and rapid method for therapeutic drug monitoring compared to traditional immunoassay systems.

Bismuthene, a two-dimensional nanostructured material derived from the environmentally friendly and nontoxic element bismuth, holds significant potential for sustainable electrocatalytic applications. However, the large-scale application of bismuthene is hindered by the absence of a high-throughput method for synthesizing solution-processable bismuthene nanosheets, which are essential for the straightforward and low-cost fabrication of bismuthene-based nanostructure devices. This study introduces a simple solvothermal method for synthesizing bismuthene nanosheets, using hexamethylenetetramine (HMTA) as a structure-directing agent and in situ-generated hydrogen (H₂) from the alkaline hydrolysis of NaBH4 as the reducing agent. The structural and electron transfer properties were characterized by using microscopic, spectroscopic, and electrochemical analyses. To demonstrate the electrocatalytic application potential, a bismuthene-modified screen-printed carbon nanotube electrode was fabricated as a nanosensor for the quantitative detection of heavy metal ions in contaminated water. The nanosensor exhibited a wide linear concentration range and low detection limits of 0.1 and 0.16 ppb (μg/L) for Cd and Pb, respectively. Additionally, the sensor was integrated with a microfluidic flow cell, demonstrating its applicability for the flow-through analysis of Cd and Pb ions. The nanosensor showed high selectivity for Cd and Pb ions in the presence of other metal ions with excellent repeatability and sensor-to-sensor reproducibility, evidenced by a relative standard deviation of 2% and 10%, respectively.

A single run approach for rapid detection of nitrification inhibitor, dicyandiamide (DCD) using electrogenerated chlorine assisted polymerization through azo bond, under acidic conditions and at a preanodized screen printed carbon electrode (SPCE*) is presented. The role of chloride containing support electrolyte in acidic medium along with oxygen functionalities/edge sites are found to be crucial for the successful oxidative polymerization and subsequent adsorption of oxidized products on the electrode surface. The SEM, cyclic voltammetry and X-ray photoelectron spectroscopy studies were used to characterize the polymer film formation. The system exhibited a linear range between 20 and 170 μM with a detection limit of 3 μM (S/N = 3). The method was successfully tested for the detection of DCD in dairy and water samples. Simultaneous detection of DCD in the presence of melamine has also been demonstrated.

A new technique for sensing nanomolar concentrations of hydrazine in water samples is reported. A screen-printed carbon electrode (SPCE) altered using an amine-azo functional group encompassing poly(dicyandiamide) is used in this study. The modified electrode exhibits an enhanced activity toward hydrazine detection at a lower overpotential and broad linear scale between 20 nM and 1 mM, with an accurate sensitivity value of 0.1 nA μm–1 cm–2. To the best of our knowledge, poly(dicyandiamide)-modified electrodes exhibit one of the lowest limits of detection for any metal-free electrode that detects 6.7 nM (S/N = 3) of hydrazine. The method established sufficient selectivity and better recoveries. Finally, the poly(dicyandiamide)-modified SPCE* is highly suitable for electrochemical determination of hydrazine in water samples from tap and lake.

In this study, nanostructure kazakhstanite-like iron vanadate (FexV3xOy.H2O) was synthesized and calcined at different temperatures (100-800 °C) in a nitrogen atmosphere. The material was used to modify screen-printed carbon electrodes to achieve an electrocatalytic effect on the surface. The relationship between calcination conditions and the catalytic performance of the electrode towards the oxidation of chemotherapeutic drugs, including methotrexate (MTX) and folinic acid (FA), was studied. Various spectroscopic, microscopic, and electrochemical methods were used to characterize the synthesized materials. The results show that calcination induces changes in the electronic structure, nanostructure morphology, electroactive surface area, and electrocatalytic performance of the material. Screen-printed carbon electrode modified with FexV3xOy calcinated at 450 °C (SPC/FexV3xOy-450) was used to develop a voltammetric sensor for the determination of MTX and FA in blood serum. The response of the SPC/FexV3xOy-450 towards the electrooxidation of MTX and FA was the highest in comparison to the bare SPC and SPC/FexV3xOy calcined at other temperatures. The SPC/FexV3xOy-450 exhibited a linear relationship over a wide concentration range: 0.005-200 µM for MTX and 0.05-200 µM for FA. The detection limit was 2.85 nM for MTX and 7.79 nM for FA. Compared to conventional methods, the SPC/FexV3xOy-450 sensor had a short response time (5 min) for simultaneous detection of MTX and FA without signal interferences from coexisting electroactive compounds. The accurate and precise determination of MTX in the presence of FA confirmed the potential clinical applications of SPC/FexV3xOy-450 for therapeutic drug monitoring during chemotherapy.