Determination of chromium valence over the range Cr(0)-Cr(VI) by electron energy loss spectroscopy

被引:128
作者
Daulton, Tyrone L. [1 ]
Little, Brenda J.
机构
[1] Washington Univ, Ctr Mat Innovat, St Louis, MO 63130 USA
[2] USN, Res Lab, Stennis Space Ctr, Marine Geosci Div, Stennis Space Ctr, MS 39529 USA
[3] USN, Res Lab, Stennis Space Ctr, Div Oceanog, Stennis Space Ctr, MS 39529 USA
关键词
electron energy loss spectroscopy; chromium valence determination; L-2; L-3-adsorption edges; transmission electron microscopy;
D O I
10.1016/j.ultramic.2006.02.005
中图分类号
TH742 [显微镜];
学科分类号
摘要
Chromium is a redox active 3d transition metal with a wide range of valences (-2 to + 6) that control the geochemistry and toxicity of the element. Therefore, techniques that measure Cr valence are important bio/geochemical tools. Until now, all established methods to determine Cr valence were bulk techniques with many specific to a single, or at best, only a few oxidation state(s). We report an electron energy loss spectroscopy (EELS) technique along with an extensive suite of affined reference spectra that together, unlike other methods, can determine Cr valence (or at least constrain the possible valences) at high-spatial resolution (tens-of-nanometer scale) across a wide valence range, Cr(0)-Cr(VI). Fine structure of Cr-L-2,L-3 edges was parametrized by measurement of the chemical shift of the L-3 edge and the ratio of integrated intensity under the L-3 and L-2 edges. These two parameterizations were correlated to Cr valence and also the d" orbital configuration which has a large influence on L-edge fine structure. We demonstrate that it is not possible to unambiguously determine Cr valence from only one fine-structure parameterization which is the method employed to determine metal valence by nearly all previous EELS studies. Rather, multiple fine-structure parameterizations must be used together if the full range of possible Cr valences is considered. However even with two parameterizations, there are limitations. For example, distinguishing Cr(IV) from Cr(HI) is problematic and it may be difficult to distinguish low-spin Cr(H) from Cr(III). Nevertheless, when Cr is known to be divalent, low- and bigh-spin d" orbital configurations can be readily distinguished. Published by Elsevier B.V.
引用
收藏
页码:561 / 573
页数:13
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