Continuous and considerable exploration of two–dimensional transition metal carbides and nitrides (MXenes)toward interlayer spacing expansion, surface termination modification and composition architecture construction has aroused significant interest in energy storage fields. Nevertheless, their employment remains severely impeded by a fundamental lack of comprehension of the coordination chemistry of MXenes. Herein, hierarchical porous N‐doped carbon encapsulated fluorine‐free Ti3C2Tx with tunable coordination chemistry is fabricated by a novel one‐pot etching strategy. The Ti coordinated with N manipulated by phase reconstruction is identified by high‐angle annular dark‐field scanning transmission electron microscopy and X‐ray photoelectron spectroscopy. Moreover, hierarchical porous nitrogen‐doped carbons (HPNC) are distinctly observed that result in a multifold increase in material surface area derived from a substantial increment of micro‐ and mesoporosity. The structural synergistic effect of Ti coordinated with N, and HPNC heighten binding energy and reduce energy barriers that accelerate redox kinetics, and boosts physical immobilization of lithium polysulfides. The aforementioned MXenes modified separators endow lithium–sulfur batteries with a reversible capacity of 889.5 mA h g−1 with capacity retention of 79.5% after 100 cycles at 0.5 A g−1. Overall, this work affords a novel and universal etching strategy in terms of directly synthesizing fluoride‐free MXene with tunable coordination chemistry toward exploring the correlation between structural and electrochemical properties.
Introduction: Testosterone is a steroid that can help with blood disorders, sexual dysfunctions, connective tissue diseases, some malignancies, intractable pain, and other serious diseases. However, it must be prescribed under medical supervision because of the risk of major adverse effects such as liver disease, heart disease, stroke, blood clots, and cancer. There is an urgent need for research on developing an electrochemical sensor to detect testosterone as a doping substance in sports. Objective: Develop an electrochemical sensor of poly(ionic liquid)-graphene oxide molecularly printed polymers (PIL/MIs/GO) to detect testosterone as a doping substance in sports. Methods: Morphological characterization of modified electrodes was performed by field emission scanning electron microscopy (FESEM), allowing the GO to be surface-mounted with fragments and apertures. Due to the holes generated by the agglomeration of PIL and MIs molecules on the wavy edges of the GO nanosheets, the surface morphology of PIL/MIs/GO/GCE also revealed a high porosity structure. Results: Compared to other synergistic influences of GO nanosheets with PIL and MIs molecules, electrochemical investigations using a differential pulse voltammetry approach indicated high selectivity, good stability, appropriate linear range, lower detection limit, and higher selectivity. Conclusion: In pharmaceutical samples and human biological fluids, the validity and accuracy of PIL/MIs/GO/GCE for the determination of testosterone demonstrated practical application. PIL/MIs/GO/GCE can thus be used as an accurate and reliable sensor for detecting testosterone as a doping agent in sports. Level of evidence II; Therapeutic studies - investigation of treatment outcomes.
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