材料科学
无定形固体
微观结构
碳纤维
结晶度
玻璃碳
无定形碳
相(物质)
钻石
化学物理
化学工程
纳米技术
碳化物衍生碳
富勒烯
类金刚石碳
碳膜
石墨
吉布斯自由能
复合材料
相变
压缩(物理)
四面体
结晶学
压力(语言学)
矿物学
作者
Alan G. Salek,Qingbo Sun,Xingshuo Huang,David Robert McKenzie,Andrew V. Martin,Nigel A. Marks,J. E. Bradby,Dougal G. McCulloch
出处
期刊:Carbon
[Elsevier BV]
日期:2025-10-18
卷期号:247: 120952-120952
被引量:1
标识
DOI:10.1016/j.carbon.2025.120952
摘要
Four carbon phases including amorphous, cubic, and hexagonal forms of diamond as well as graphite were found through transmission electron microscopy analysis after non-hydrostatically compressing glassy carbon to 145 GPa at room temperature. Crystallinity and preferred orientation of the recovered phases indicate that shear stress is critical in driving the phase transformations from the sp2-bonded carbon precursor. A Gibbs free energy landscape, as a function of density and crystallinity, illustrates proposed transformation pathways from glassy carbon to a common high-density parent phase that then converts to the phases observed, depending on the local stress environment in the sample. We show how it is possible for four distinct recoverable phases of carbon to form from the glassy carbon precursor following compression in a non-hydrostatic environment. Our approach creates nanodiamonds with a wide range of sizes down to ~2 nm which have potential application as a source of custom-sized nanodiamonds for applications in biomedical and quantum sensing applications.
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