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Pyridine Adsorption for Probing Electron-Acceptor Sites on the Surface of Titanium Oxide with Supported Silver, Copper, and Gold Ions

机译:吡啶吸附用于探测负载有银,铜和金离子的氧化钛表面上的电子受体位点

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摘要

The results of investigation of the adsorption kinetics of pyridine (Py) show that the M+z = Ag+, Cu+2, and Au+3 ions supported on the surface of TiO2 (anatase) significantly increase its electron-acceptor properties. Two types of M+z/TiO2 adsorption sites are characterized by the various numbers of the pyridine coordination centers M and their oxidation states. Linear correlations between the rate constants of pyridine adsorption and the ionic radii are observed in the cases of both types of sites. The adsorption stoichiometry of the less active sites is Py-2M, where M = Cu+, Au+, and Ag-0. The linear dependence of the antibacterial activity of M+z/TiO2 on the ionic charge z = +1 (for Ag), +2 (for Cu), and +3 (for Au), as well as the ability of bacteria to reduce dissolved silver and gold ions and those supported on TiO2 to colloidal metals, is also found.
机译:吡啶(Py)吸附动力学的研究结果表明,负载在TiO2(锐钛矿)表面上的M + z = Ag +,Cu + 2和Au + 3离子显着提高了其电子受体性能。两种类型的M + z / TiO2吸附位点的特征是吡啶配位中心M的数量不同以及它们的氧化态。在两种类型的位点的情况下,观察到吡啶吸附的速率常数与离子半径之间的线性相关性。活性较低的位置的吸附化学计量为Py-2M,其中M = Cu +,Au +和Ag-0。 M + z / TiO2的抗菌活性对离子电荷z = +1(对于Ag),+ 2(对于Cu)和+3(对于Au)以及细菌还原能力的线性依赖性还发现了溶解的银和金离子以及负载在TiO2上的胶体金属。

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