【摘要】 采用FT-IR、X射线光电子能谱以及基于周期平面波的DFT方法分别研究了乙酰氧肟酸钠(aHA)在针铁矿或赤铁矿表面上的吸附结构,并将计算得到的光电子能谱移动和电荷转移实验得到的XPS结果进行对比.红外结果显示aHA可能以五元环螫合物形式吸附于针铁矿或赤铁矿表面,DFT计算结果表明aHA中氧肟酸基团的两个氧原子与针铁矿(101)或(100)表面上的一个铁原子形成五元环结构,同时氧肟酸基团中的两个氧还相应的与针铁矿表面邻近两个铁原子成键,但氧肟酸基团中的两个氧原子却只与赤铁矿(001)表面上的一个铁原子形成五元环结构.对于针铁矿(101)、(100)和赤铁矿(001)表面上吸附位点对应的铁原子,计算得到的光电子能谱移动与实验得到的光电子能谱移动基本相等,说明了计算结果的可靠性和所得吸附结构的合理性.更多还原

【Abstract】 The adsorption of sodium acetohydroxamate on the goethite or hematite surface was investigated by Fourier transform infrared spectroscopy(FT-IR),X-ray photoemission spectroscopy and periodic plane-wave density functional theory(DFT) calculations.The core-level shifts and charge transfers of the adsorbed surface iron sites calculated by DFT with periodic interfacial structures were confronted to the X-ray photoemission experiments.FT-IR results reveal that the interfacial structure of sodium acetohydroxamate adsorbed on the goethite or hematite surface may be assigned to a five-membered ring complex.In agreement with the adsorption energies determined by the DFT calculations,a five-membered ring complex is formed via bonding of one surface iron atom of goethite(101) or (100) to both oxygen atoms of hydroxamate group,and these two oxygen atoms of the hydroxamate group correspondingly attach to two neighboring iron atoms of the goethite surface.But a five-membered ring complex between two oxygen atoms of the hydroxamate group and one surface iron atom of hematite(001) is formed without any extra attachments.The calculated core-level shifts of Fe2p for the interfacial structures are correspondingly in good agreement with the experimental observed one,which confirmed the reliability of the calculated results.更多还原