Science. 1987 Nov 6;238(4828):783-6. doi: 10.1126/science.238.4828.783.
A novel application of x-ray absorption spectroscopy has provided structural information for ions sorbed at oxide-water interfaces. As an example, in situ extended x-ray absorption fine structure (EXAFS) measurements of adsorbed selenate and selenite ions at ah alpha-FeOOH(goethite)-water interface have been performed; these measurements show that selenate forms a weakly bonded, outer-sphere complex and that selenite forms a strongly bonded, inner-sphere complex. The selenite ion is bonded directly to the goethite surface in a bidentate fashion with two iron atoms 3.38 angstroms from the selenium atom. Adsorbed selenate has no iron atom in the second coordination shell of selenium, which indicates retention of its hydration sphere upon sorption. This method provides direct structural information for adsorbed species at solid-liquid interfaces.
X 射线吸收光谱学的一种新应用为氧化物-水界面上吸附离子提供了结构信息。例如,在原位扩展 X 射线吸收精细结构(EXAFS)测量中,对吸附在 α-FeOOH(针铁矿)-水界面上的硒酸盐和亚硒酸盐离子进行了测量;这些测量表明,硒酸盐形成了一个弱键合的外层络合物,而亚硒酸盐形成了一个强键合的内络合物。亚硒酸盐离子以双齿配位的方式与两个铁原子直接键合,硒原子与铁原子的距离为 3.38 埃。吸附的硒酸盐在硒的第二配位壳层中没有铁原子,这表明在吸附时保留了其水合层。这种方法为固-液界面上吸附物种提供了直接的结构信息。