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无机层状材料的巨大膨胀:通向分子级薄二维纳米片的桥梁。

Gigantic swelling of inorganic layered materials: a bridge to molecularly thin two-dimensional nanosheets.

机构信息

International Center for Materials Nanoarchitectonics, National Institute for Materials Science , 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.

出版信息

J Am Chem Soc. 2014 Apr 9;136(14):5491-500. doi: 10.1021/ja501587y. Epub 2014 Mar 31.

Abstract

Platy microcrystals of a typical layered material, protonated titanate, have been shown to undergo an enormous degree of swelling in aqueous solutions of various amines, including tertiary amines, quaternary ammonium hydroxides, and primary amines. Introducing these solutions expanded the crystal gallery height by up to ~100-fold. Through systematic analysis, we determined that ammonium ion intercalation is predominantly affected by the acid-base equilibrium and that the degree of swelling or inflow of H2O is controlled by the osmotic pressure balance between the gallery and the solution environment, both of which are relatively independent of electrolyte identity but substantially dependent on molarity. In solutions of tertiary amines and quaternary ammonium hydroxides, the uptake of ammonium ions increases nearly linearly with increasing external concentration before reaching a saturation plateau, i.e., ~40% relative to the cation-exchange capacity of the crystals used. The only exception is tetrabutylammonium ions, which yield a lower saturation value, ~30%, owing to steric effects. The swelling behaviors in some primary amine solutions differ as a result of the effect of attractive forces between amine solute molecules on the solution osmotic pressure. Although the swelling is essentially colligative in nature, the stability of the resultant swollen structure is heavily dependent on the chemical nature of the guest ions. Intercalated ions of higher polarity and smaller size help stabilize the swollen structure, whereas ions of lower polarity and larger size lead readily to exfoliation. The insight gained from this study sheds new light on both the incorporation of guest molecules into a gallery of layered structures in general and the exfoliation of materials into elementary single-layer nanosheets.

摘要

层状材料质子化钛酸盐的典型薄片微晶体已被证明在各种胺类水溶液中(包括叔胺、季铵氢氧化物和伯胺)会发生极大的溶胀。引入这些溶液将晶体层间高度扩展了高达100 倍。通过系统分析,我们确定铵离子的嵌入主要受酸碱平衡的影响,而溶胀或 H2O 的流入程度由层间和溶液环境之间的渗透压平衡控制,这两者都相对独立于电解质的种类,但在很大程度上取决于摩尔浓度。在叔胺和季铵氢氧化物溶液中,铵离子的摄取量在达到饱和平台之前几乎随外部浓度线性增加,即在40%的晶体阳离子交换容量范围内。唯一的例外是四丁基铵离子,由于空间位阻效应,其饱和值约为~30%。由于溶质分子之间的吸引力对溶液渗透压的影响,一些伯胺溶液中的溶胀行为有所不同。尽管溶胀本质上是依数性的,但所得溶胀结构的稳定性在很大程度上取决于客体离子的化学性质。具有更高极性和更小尺寸的插层离子有助于稳定溶胀结构,而具有较低极性和较大尺寸的离子则容易导致剥离。这项研究的结果为一般将客体分子纳入层状结构的层间以及将材料剥离成基本单层纳米片提供了新的认识。

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