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利用 STEM-EELS 监测混合价态 Fe(氧氢)氧化物(绿锈)的束诱导氧化。

Beam-induced oxidation of mixed-valent Fe (oxyhydr)oxides (green rust) monitored by STEM-EELS.

机构信息

GFZ German Research Center for Geosciences, Telegrafenberg, 14473, Potsdam, Germany; School of Chemical and Process Engineering, University of Leeds, Leeds, LS2 9JT, United Kingdom.

GFZ German Research Center for Geosciences, Telegrafenberg, 14473, Potsdam, Germany; Department of Earth Sciences, Free University of Berlin, 12249, Berlin, Germany.

出版信息

Micron. 2019 Jul;122:46-52. doi: 10.1016/j.micron.2019.02.002. Epub 2019 Feb 10.

Abstract

Analytical transmission electron microscopy (TEM) is often used to investigate morphologies, crystal structures, chemical compositions and oxidation states of highly reactive mixed-valent mineral phases. Of prime interest, due to its potential role in toxic metal remediation, is green rust sulphate (GR) an Fe-Fe layered double hydroxide. In this study, we quantified the effects that TEM analysis has on GR in order to ensure the measured material properties are a result of synthesis and reaction kinetics, and not due to sample preparation and analysis technique. To do this, we compared two sample preparation techniques (anoxic drop-cast with drying, and frozen-hydrated cryogenic) and exposed samples to the electron beam for several minutes, acquiring fluence series between ca. 40 e Å and 10,000 e Å. TEM imaging and electron diffraction showed that the hexagonal plate-like morphology and crystal structure of GR were largely unaffected by sample preparation and analysis technique. However, quantitative analysis of a series of monochromated Fe L-edge electron energy loss spectra (EELS) showed that electron irradiation induces oxidation. We measured an Fe(II)/Fe(III) ratio of 1.94 (as expected for GR) at 50 e Å. However, above this fluence, the ratio logarithmically decreased and dropped to ca. 0.5 after 1000 e Å. This trend was approximately the same for both sample preparation techniques implying that it is the beam alone which causes valence state changes, and not exposure to oxygen during transfer into the TEM or the vacuum of the TEM column. Ultimately this work demonstrates that GR valence can be quantified by EELS provided that the sample is not over exposed to electrons. This also opens the possibility of quantifying the effect of redox-sensitive toxic metals (e.g., As, Cr, Se) on Fe oxidation state in GR phases (relevant to the treatment of contaminated soils and water) with a higher spatial resolution than other techniques (e.g., Mössbauer spectroscopy).

摘要

分析电子显微镜(TEM)常用于研究高反应性混合价矿物相的形貌、晶体结构、化学成分和氧化态。由于其在有毒金属修复中的潜在作用,绿锈硫酸盐(GR)——一种 Fe-Fe 层状双氢氧化物,受到了极大的关注。在这项研究中,我们量化了 TEM 分析对 GR 的影响,以确保测量的材料特性是合成和反应动力学的结果,而不是由于样品制备和分析技术的原因。为此,我们比较了两种样品制备技术(缺氧滴铸干燥法和冷冻水合低温法),并使样品暴露在电子束下几分钟,获得了约 40eÅ 和 10000eÅ 之间的通量系列。TEM 成像和电子衍射表明,GR 的六方板状形貌和晶体结构在很大程度上不受样品制备和分析技术的影响。然而,一系列单色化的 Fe L 边电子能量损失谱(EELS)的定量分析表明,电子辐照会引起氧化。我们在 50eÅ 处测量到 Fe(II)/Fe(III) 比值为 1.94(与 GR 预期值相符)。然而,在此通量以上,比值对数下降,在 1000eÅ 后降至约 0.5。两种样品制备技术的趋势大致相同,这表明是电子束本身导致了价态的变化,而不是在 TEM 或 TEM 柱的真空环境中转移过程中暴露于氧气。最终,这项工作表明,只要样品不被过度暴露于电子,EELS 就可以定量测定 GR 的价态。这也为利用 EELS 以比其他技术(如穆斯堡尔光谱学)更高的空间分辨率来定量测定 GR 相中氧化还原敏感的有毒金属(如 As、Cr、Se)对 Fe 氧化态的影响提供了可能性。

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