Synergy for Enhancing Strength and Toughness of Diamond through Polytypic Heterointerface

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry C Pub Date : 2025-03-29 DOI:10.1021/acs.jpcc.5c00702
Tengfei Xu, Zhaorui Liu, Dominik Legut, Ruifeng Zhang
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Abstract

Hierarchical diamond nanocomposites, incorporating diverse coherently interfaced diamond polytypes, exhibit remarkable fracture toughness while maintaining exceptional hardness. However, the underlying mechanisms governing the strengthening and toughening of these polytypic heterointerfaces (PHIs) remain elusive. In this study, we employed first-principles approaches to derive the ideal strength and Peierls stress, conducting a comprehensive investigation into the influence of various PHIs on the plasticity of nanostructured diamond. A ubiquitous strengthening effect was observed across all PHI types under uniform shear deformation, as the introduction of PHIs invariably aligned a portion of the crystal in the hard shear direction, yielding strength comparable to that of the nanotwinned diamond. Surprisingly, graphitization and bond collapse were suppressed through a sequential transformation of stacking sequences, including an experimentally observed non-3C to 3C polytype transition. This phenomenon was attributed to the systematic bond realignment driven by continuous metallization confined to specific atomic layers. The heterointerface-mediated bonding reorganization effectively dissipated energy through phase transitions, thereby achieving supertoughness. Under localized deformation, all PHIs were found to enhance the barrier against parallel slip of 1/2 ⟨110⟩ shuffle-set full dislocations and 1/6 ⟨112⟩ glide-set partial dislocations, leading to a pronounced strengthening effect. These findings not only deepen our fundamental understanding of the synergistic strengthening and toughening of diamond through PHIs but also offer valuable insights for the design of other superhard materials and engineering ceramics via coherent heterointerfaces.

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通过多型异质界面协同提高金刚石的强度和韧性
层叠金刚石纳米复合材料,包含了不同的相干界面金刚石多型,在保持优异硬度的同时表现出显著的断裂韧性。然而,控制这些多型异质界面(PHIs)强化和增韧的潜在机制仍然是难以捉摸的。在本研究中,我们采用第一性原理的方法推导出理想强度和佩尔斯应力,全面研究了不同ph值对纳米结构金刚石塑性的影响。在均匀剪切变形下,在所有类型的PHI中都观察到普遍存在的强化效应,因为PHI的引入总是使晶体的一部分在硬剪切方向上对齐,屈服强度与纳米孪晶金刚石相当。令人惊讶的是,石墨化和键崩溃通过堆叠序列的顺序转换被抑制,包括实验观察到的非3C到3C多型转变。这一现象归因于连续金属化在特定原子层中驱动的系统键重新排列。异质界面介导的键重组通过相变有效地耗散能量,从而实现超韧性。在局部变形下,所有的PHIs都被发现增强了对1/2⟨110⟩滑动集完全错位和1/6⟨112⟩滑动集部分错位平行滑动的屏障,导致明显的强化效果。这些发现不仅加深了我们对通过聚类异质界面对金刚石进行协同强化和增韧的基本认识,而且为通过相干异质界面设计其他超硬材料和工程陶瓷提供了有价值的见解。
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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