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富勒烯-立方烷反应诱导的非晶碳团簇的新有序结构。

New Ordered Structure of Amorphous Carbon Clusters Induced by Fullerene-Cubane Reactions.

机构信息

State Key Laboratory of Superhard Materials, College of Physics, Jilin University, Changchun, 130012, China.

College of Science, Civil Aviation University of China, Tianjin, 300300, China.

出版信息

Adv Mater. 2018 May;30(22):e1706916. doi: 10.1002/adma.201706916. Epub 2018 Apr 15.

Abstract

As a new category of solids, crystalline materials constructed with amorphous building blocks expand the structure categorization of solids, for which designing such new structures and understanding the corresponding formation mechanisms are fundamentally important. Unlike previous reports, new amorphous carbon clusters constructed ordered carbon phases are found here by compressing C H /C cocrystals, in which the highly energetic cubane (C H ) exhibits unusual roles as to the structure formation and transformations under pressure. The significant role of C H is to stabilize the boundary interactions of the highly compressed or collapsed C clusters which preserves their long-range ordered arrangement up to 45 GPa. With increasing time at high pressure, the gradual random bonding between C H and carbon clusters, due to "energy release" of highly compressed cubane, leads to the loss of the ability of C H to stabilize the carbon cluster arrangement. Thus a transition from short-range disorder to long-range disorder (amorphization) occurs in the formed material. The spontaneous bonding reconstruction most likely results in a 3D network in the material, which can create ring cracks on diamond anvils.

摘要

作为一种新型的固体,由无定形结构单元构建的结晶材料扩展了固体的结构分类,设计这类新材料的结构并理解其相应的形成机制是至关重要的。与以往的报道不同,通过压缩 C H /C 共晶,在这里发现了由新的无定形碳团簇构建的有序碳相,其中高能量的立方烷(C H )在高压下的结构形成和转变中表现出异常的作用。C H 的重要作用是稳定高度压缩或坍塌的 C 团簇的边界相互作用,从而在 45GPa 下保持其长程有序排列。随着高压下时间的延长,由于高度压缩立方烷的“能量释放”,C H 与碳团簇之间逐渐发生随机键合,导致 C H 稳定碳团簇排列的能力丧失。因此,在形成的材料中发生了从短程无序到长程无序(非晶化)的转变。这种自发的键合重构很可能导致材料中形成 3D 网络,从而在金刚石砧上产生环状裂纹。

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