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氧化镁立方体的水合作用:一项氦离子显微镜研究。

Hydration of magnesia cubes: a helium ion microscopy study.

作者信息

Schwaiger Ruth, Schneider Johannes, Bourret Gilles R, Diwald Oliver

机构信息

Institute for Applied Materials (IAM) and Karlsruhe Nano Micro Facility (KNMF), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, D-76344 Eggenstein-Leopoldshafen, Germany.

Department of Chemistry and Physics of Materials, University of Salzburg, Hellbrunnerstrasse 34/ III, A-5020 Salzburg, Austria.

出版信息

Beilstein J Nanotechnol. 2016 Feb 29;7:302-9. doi: 10.3762/bjnano.7.28. eCollection 2016.

Abstract

Physisorbed water originating from exposure to the ambient can have a strong impact on the structure and chemistry of oxide nanomaterials. The effect can be particularly pronounced when these oxides are in physical contact with a solid substrate such as the ones used for immobilization to perform electron or ion microscopy imaging. We used helium ion microscopy (HIM) and investigated morphological changes of vapor-phase-grown MgO cubes after vacuum annealing and pressing into foils of soft and high purity indium. The indium foils were either used as obtained or, for reference, subjected to vacuum drying. After four days of storage in the vacuum chamber of the microscope and at a base pressure of p < 10(-7) mbar, we observed on these cubic particles the attack of residual physisorbed water molecules from the indium substrate. As a result, thin magnesium hydroxide layers spontaneously grew, giving rise to characteristic volume expansion effects, which depended on the size of the particles. Rounding of the originally sharp cube edges leads to a significant loss of the morphological definition specific to the MgO cubes. Comparison of different regions within one sample before and after exposure to liquid water reveals different transformation processes, such as the formation of Mg(OH)2 shells that act as diffusion barriers for MgO dissolution or the evolution of brucite nanosheets organized in characteristic flower-like microstructures. The findings underline the significant metastability of nanomaterials under both ambient and high-vacuum conditions and show the dramatic effect of ubiquitous water films during storage and characterization of oxide nanomaterials.

摘要

因暴露于环境中而产生的物理吸附水会对氧化物纳米材料的结构和化学性质产生强烈影响。当这些氧化物与固体基底(如用于固定以进行电子或离子显微镜成像的基底)物理接触时,这种影响可能会尤为显著。我们使用氦离子显微镜(HIM),研究了气相生长的氧化镁立方体在真空退火并压制成柔软高纯度铟箔后的形态变化。铟箔要么直接使用,要么作为参照进行真空干燥。在显微镜的真空腔中、基础压力p < 10⁻⁷ mbar的条件下储存四天后,我们在这些立方颗粒上观察到来自铟基底的残留物理吸附水分子的侵蚀。结果,氢氧化镁薄层自发生长,产生了取决于颗粒尺寸的特征性体积膨胀效应。原本尖锐的立方体边缘变圆,导致氧化镁立方体特有的形态清晰度显著丧失。对一个样品在暴露于液态水前后的不同区域进行比较,揭示了不同的转变过程,例如形成作为氧化镁溶解扩散屏障的氢氧化镁壳层,或形成具有特征性花状微观结构的水镁石纳米片。这些发现强调了纳米材料在环境和高真空条件下的显著亚稳定性,并展示了无处不在的水膜在氧化物纳米材料储存和表征过程中的巨大影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6059/4901542/752f9c57e50d/Beilstein_J_Nanotechnol-07-302-g002.jpg

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