3 research outputs found

    Two-Dimensional Titanium Nitride (Ti<sub>2</sub>N) MXene: Synthesis, Characterization, and Potential Application as Surface-Enhanced Raman Scattering Substrate

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    We report on the synthesis, characterization, and application of Ti<sub>2</sub>N (MXene), a two-dimensional transition metal nitride of M<sub>2</sub>X type. Synthesis of nitride-based MXenes (M<sub><i>n</i>+1</sub>N<sub><i>n</i></sub>) is difficult due to their higher formation energy from M<sub><i>n</i>+1</sub>AN<sub><i>n</i></sub> and poor stability of M<sub><i>n</i>+1</sub>N<sub><i>n</i></sub> layers in the etchant employed, typically HF. Herein, the selective etching of Al from ternary layered transition metal nitride Ti<sub>2</sub>AlN (MAX) and intercalation were achieved by immersing the powder in a mixture of potassium fluoride and hydrochloric acid. The multilayered Ti<sub>2</sub>NT<sub><i>x</i></sub> (T is the surface termination) obtained was sonicated in DMSO and centrifuged to obtain few-layered Ti<sub>2</sub>NT<sub><i>x</i></sub>. MXene formation was verified, and the material was completely characterized by Raman spectroscopy, XRD, XPS, FESEM-EDS, TEM, STM, and AFM techniques. Surface-enhanced Raman scattering (SERS) activity of the synthesized Ti<sub>2</sub>NT<sub><i>x</i></sub> was investigated by fabricating paper, silicon, and glass-based SERS substrates. A Raman enhancement factor of 10<sup>12</sup> was demonstrated using rhodamine 6G as the model compound with 532 nm excitation wavelength. Detection of trace level explosives with a simple paper-based SERS substrate with Ti<sub>2</sub>N (MXene) as active material was also illustrated

    A Novel Biomass Derived Carbon Quantum Dots for Highly Sensitive and Selective Detection of Hydrazine

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    We report for the first time, carbon quantum dots (CQD) based highly sensitive and selective electrochemical sensor for detection of hydrazine. CQD was synthesized by pyrolysis method using a natural precursor, chia seeds. The sensing ability was studied in terms of oxygen‐rich functional groups present on the surface of CQD
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