首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Covalent functionalization of MoS2 nanosheets synthesized by liquid phase exfoliation to construct electrochemical sensors for Cd (II) detection
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Covalent functionalization of MoS2 nanosheets synthesized by liquid phase exfoliation to construct electrochemical sensors for Cd (II) detection

机译:液相剥离合成的MOS2纳米片的共价官能化,构建CD(II)检测的电化学传感器

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Surface functionalization is an effective strategy in the precise control of electronic surface states of twodimensional materials for promoting their applications. In this study, based on the strong coordination interaction between the transition-metal centers and N atoms, the surface functionalization of few-layer MoS2 nanosheets was successfully prepared by liquid phase exfoliation method in N, N-dimethylformamide (DMF), 1-methyl-2-pyrrolidinone, and formamide. The cytotoxicity of surface-functionalized MoS2 nanosheets was for the first time evaluated by the methylthiazolyldiphenyl-tetrazoliumbromide assays. An electrochemical sensor was constructed based on glass carbon electrode (GCE) modified by MoS2 nanosheets obtained in DMF, which exhibits relatively higher sensitivity to Cd2+ detection and lower cytotoxicity against MCF-7 cells. The mechanisms of surface functionalization and selectively detecting Cd2+ were investigated by density functional theory calculations together with various spectroscopic measurements. It was found that surface-functionalized MoS2 nanosheets could be generated through Mo-N covalent bonds due to the orbital hybridization between the 5 s orbitals of Mo atoms and the 2p orbitals of N atoms of the solvent molecules. The high selectivity of the sensor is attributed to the coordination reaction between Cdz+ and O donor atoms of DMF adsorbed on MoS2 nanosheets. The robust anti-interference is ascribed to the strong binding energy of Cd2+ and O atoms of DMF. Under the optimum conditions, the electrochemical sensor exhibits highly sensitive and selective assaying of Cd2+ with a measured detection limit of 0.2 nM and a linear range from 2 nM to 20 mu M.
机译:表面官能化是一种有效的策略,可精确控制用于促进其应用的两模州材料的电子表面状态。在该研究中,基于过渡金属中心和N原子之间的强配位相互作用,通过N,N-二甲基甲酰胺(DMF),1-甲基的液相剥离方法成功地制备了几层MOS2纳米晶片的表面官能化。 -2-吡咯烷酮和甲酰胺。表面官能化MOS2纳米片的细胞毒性首次由甲基噻唑苯二酚 - 四唑溴铵测定评估。基于在DMF中获得的MOS2纳米片改性的玻璃碳电极(GCE)构建电化学传感器,其对CD2 +检测和对MCF-7细胞的降低细胞毒性表现出相对较高的敏感性。通过密度官能理论计算研究了表面官能化和选择性地检测CD2 +的机制,以及各种光谱测量。结果发现,由于钼原子的5秒轨道与溶剂分子的N原子的2p轨道之间的轨道杂交,可以通过Mo-N共价键产生表面官能化MOS2纳米蛋白酶。传感器的高选择性归因于DMF的CDZ +和O供体原子之间的配位反应吸附在MOS2纳米晶片上。稳健的抗干扰归因于DMF的CD2 +和O原子的强粘合能。在最佳条件下,电化学传感器对CD2 +具有高度敏感和选择性测定,测量的检测限为0.2nm,线性范围为2nm至20μm。

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