Crystallisation in biomineral mollusc shell studied by 3D Bragg ptychography.

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL
Tilman A Grünewald, Peng Li, Julien Duboisset, Julius Nouet, Oier Bikondoa, Jeremie Vidal-Dupiol, Denis Saulnier, Manfred Burghammer, Virginie Chamard
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引用次数: 0

Abstract

Biomineralisation integrates complex biologically assisted physico-chemical processes leading to an extraordinary diversity of calcareous biomineral crystalline architectures, in intriguing contrast with the consistent presence of a submicrometric granular structure. While the repeated observation of amorphous calcium carbonate is interpreted as a precursor to the crystalline phase, the crystalline transition mechanisms are poorly understood. Access to the crystalline architecture at the mesoscale, i.e., over a few granules, is key to building realistic crystallisation models. Here we exploit three-dimensional X-ray Bragg ptychography microscopy to provide a series of nanoscale maps of the crystalline structure within the "single-crystalline" prism of the prismatic layer of a Pinctada margaritifera shell. The mesocrystalline organisation exhibits several micrometre-sized iso-oriented/iso-strained crystalline domains, the detailed studies of which reveal the presence of crystalline coherence domains ranging from 130 to 550 nm in size. The further increase in the lattice parameter with the size of the coherence domain likely results from the crystallisation mechanism, pointing towards a maturation process occurring after the initial amorphous-to-crystalline transition.

三维Bragg图谱研究生物矿物软体动物壳的结晶。
生物矿化整合了复杂的生物辅助物理化学过程,导致钙质生物矿物晶体结构的非凡多样性,与亚微米颗粒结构的一致存在形成了有趣的对比。虽然反复观察到的无定形碳酸钙被解释为结晶相的前体,但晶体转变机制却知之甚少。进入中尺度的晶体结构,即在几个颗粒上,是建立真实结晶模型的关键。在这里,我们利用三维x射线布拉格平面显微镜提供了一系列纳米尺度的晶体结构图,这些晶体结构图位于平锥藻壳的棱柱层的“单晶”棱柱内。中晶组织显示出几个微米大小的等取向/等应变晶体域,其详细研究揭示了130至550 nm大小的晶体相干域的存在。晶格参数随相干域大小的进一步增加可能是结晶机制的结果,表明在初始的非晶向结晶转变之后发生了成熟过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Faraday Discussions
Faraday Discussions 化学-物理化学
自引率
0.00%
发文量
259
期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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