Growth mechanisms of interfacial carbides in solid-state reaction between single-crystal diamond and chromium

IF 3.5 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zhuo Liu , Wei Cheng , Dekui Mu , Qiaoli Lin , Xipeng Xu , Han Huang
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引用次数: 1

Abstract

Interfacial bonding is one of the most challenging issues in the fabrication, and hence comprehensively influences the properties of diamond-based metal matrix composites (MMCs) materials. In this work, solid-state (S/S) interface reaction between single-crystal synthetic diamond and chromium (Cr) metal was critically examined with special attention given to unveil the role of crystal orientation in the formation and growth of interfacial products. It has been revealed that catalytically converted carbon (CCC) was formed prior to chromium carbides, which is counterintuitive to previous studies. Cr7C3 was the first carbide formed in the S/S interface reaction, aided by the relaxation of diamond lattices that reduces the interfacial mismatch. Interfacial Cr7C3 and Cr3C2 carbides were formed at 600 and 800 °C, respectively, with the growth preferred on diamond (100) plane, because of its higher density of surface defects than (111) plane. Interfacial strain distribution was quasi-quantitively measured using windowed Fourier Transform-Geometric Phase Analysis (WFT-GPA) analysis and an ameliorated strain concentration was found after the ripening of interfacial carbides. Textured morphologies of Cr3C2 grown on diamond (100) and (111) planes were perceived after S/S interface reaction at 1000 °C, which is reported for the first time. The underlying mechanisms of Cr-induced phase transformation on diamond surface, as well as the crystal orientation dependent growth of interfacial carbides were unveiled using the first-principles calculation. The formation and growth mechanisms of Cr3C2 were elucidated using SEM, TEM and XRD analyses. Finally, an approach for tailoring the interfacial microstructure between synthetic diamond and bonding metals was proposed.

Abstract Image

单晶金刚石与铬固相反应中界面碳化物的生长机理
界面键合是金刚石基金属基复合材料制造中最具挑战性的问题之一,它全面影响着金刚石基金属基复合材料的性能。本文对单晶人造金刚石与金属铬(Cr)之间的固态(S/S)界面反应进行了严格的研究,特别注意揭示了晶体取向在界面产物形成和生长中的作用。催化转化碳(CCC)的形成早于碳化铬,这与以往的研究结果相悖。Cr7C3是在S/S界面反应中形成的第一个碳化物,这得益于金刚石晶格的弛豫,减少了界面失配。在600℃和800℃分别形成Cr7C3和Cr3C2界面碳化物,由于金刚石(100)面表面缺陷密度高于金刚石(111)面,Cr7C3和Cr3C2界面碳化物在金刚石(100)面优先生长。采用窗口傅里叶变换-几何相位分析(WFT-GPA)准定量测量了界面应变分布,发现界面碳化物成熟后应变浓度有所改善。在1000℃条件下进行S/S界面反应,观察到生长在金刚石(100)和(111)平面上的Cr3C2的织构形貌,这是首次报道。利用第一性原理计算揭示了cr诱导金刚石表面相变的潜在机制,以及界面碳化物的晶体取向依赖生长。采用SEM、TEM和XRD等分析手段对Cr3C2的形成和生长机理进行了研究。最后,提出了一种裁剪人造金刚石与结合金属界面微观结构的方法。
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
ACS Chemical Biology
ACS Chemical Biology 生物-生化与分子生物学
CiteScore
7.50
自引率
5.00%
发文量
353
审稿时长
3.3 months
期刊介绍: ACS Chemical Biology provides an international forum for the rapid communication of research that broadly embraces the interface between chemistry and biology. The journal also serves as a forum to facilitate the communication between biologists and chemists that will translate into new research opportunities and discoveries. Results will be published in which molecular reasoning has been used to probe questions through in vitro investigations, cell biological methods, or organismic studies. We welcome mechanistic studies on proteins, nucleic acids, sugars, lipids, and nonbiological polymers. The journal serves a large scientific community, exploring cellular function from both chemical and biological perspectives. It is understood that submitted work is based upon original results and has not been published previously.
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