Reexamination of the structure of opal-A: A combined study of synchrotron X-ray diffraction and pair distribution function analysis

结晶学 无定形固体 堆积 材料科学 对分布函数 透射电子显微镜 晶体孪晶 衍射 同步加速器 方石英 柯石英 鳞石英 X射线晶体学 化学 石英 纳米技术 光学 地质学 微观结构 物理 俯冲 榴辉岩 有机化学 复合材料 古生物学 构造学 量子力学
作者
Seung-Yeol Lee,Huifang Xu,Hongwu Xu
出处
期刊:American Mineralogist [Mineralogical Society of America]
卷期号:107 (7): 1353-1360 被引量:2
标识
DOI:10.2138/am-2022-8017
摘要

Abstract The structure of opal-A was not fully understood due to its poorly crystalline nature. To better understand its structural characteristics, we have analyzed opal-AN (amorphous-network) and opal-AG (amorphous-gel) using synchrotron X-ray diffraction (XRD), pair-distribution function (PDF) analysis, and transmission electron microscopy (TEM). Opal-AN mainly exists as an aggregation of different sizes of nanospheres (<5 nm) generating banded features, whereas opal-AG displays close-packed silica nanospheres with a diameter of ~400 nm. TEM energy-dispersive X-ray spectroscopy (EDS) indicates that Na, Al, K, and Ca are present as trace elements in opal-AN and opal-AG. XRD patterns of both samples show one prominent peak at ~4.0 Å, together with broad peaks at ~2.0, ~1.45, and ~1.2 Å. Previous studies only identified the ~4.0 Å diffraction peak for the definition of opal-A. Hence, opal-A needs to be redefined by taking into account the newly observed three broad peaks. PDF patterns of opal-AN and opal-AG reveal short-range atomic pairs (<15 Å) with almost identical profiles. Both phases exhibit Si-O correlation at 1.61 Å and O-O correlation at 2.64 Å in their [SiO4] tetrahedra. The currently accepted opal structure is disordered intergrowths of cristobalite- and tridymite-like domains consisting of six-membered rings of [SiO4] tetrahedra. Our PDF analyses have identified additional, coesite-like nanodomains comprising four-membered [SiO4] rings. Moreover, we have identified eight-membered rings that can be generated by twinning and stacking faults from six-membered rings. The coesite nanodomains in opal-A may be a precursor for coesite micro-crystals formed by the impact of supersonic micro-projectiles at low pressures. More broadly, our study has also demonstrated that the combined approach of synchrotron XRD/PDF with TEM is a powerful approach to determine the structures of poorly crystallized minerals.

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