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通过键合轨道的最佳占据实现过渡金属单碳化物硬度的增强

Enhanced Hardness in Transition-Metal Monocarbides via Optimal Occupancy of Bonding Orbitals.

作者信息

Liang Yongcheng, Wei Xiao-Feng, Gu Chao, Liu Ji-Xuan, Li Fei, Yan Mingqi, Zheng Xingwei, Han Zhilin, Zhao Yusheng, Wang Shanmin, Yang Jiong, Zhang Wenqing, Kou Liangzhi, Zhang Guo-Jun

机构信息

College of Science, Institute of Functional Materials, and State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 201620, China.

Department of Physics, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.

出版信息

ACS Appl Mater Interfaces. 2021 Mar 31;13(12):14365-14376. doi: 10.1021/acsami.0c23049. Epub 2021 Mar 18.

Abstract

An efficient strategy that can guide the synthesis of materials with superior mechanical properties is important for advanced material/device design. Here, we report a feasible way to enhance hardness in transition-metal monocarbides (TMCs) by optimally filling the bonding orbitals of valence electrons. We demonstrate that the intrinsic hardness of the NaCl- and WC-type TMCs maximizes at valence electron concentrations of about 9 and 10.25 electrons per cell, respectively; any deviation from such optimal values will reduce the hardness. Using the spark plasma sintering technique, a number of WReC ( = 0-0.5) have been successfully synthesized, and powder X-ray diffractions show that they adopt the hexagonal WC-type structure. Subsequent nanoindentation and Vickers hardness measurements corroborate that the newly developed WReC samples ( = 0.1-0.3) are much harder than their parent phase (i.e., WC), marking them as the hardest TMCs for practical applications. Furthermore, the hardness enhancement can be well rationalized by the balanced occupancy of bonding and antibonding states. Our findings not only elucidate the unique hardening mechanism in a large class of TMCs but also offer a guide for the design of other hard and superhard compounds such as borides and nitrides.

摘要

一种能够指导合成具有优异机械性能材料的有效策略对于先进材料/器件设计至关重要。在此,我们报告了一种通过最佳填充价电子的成键轨道来提高过渡金属单碳化物(TMCs)硬度的可行方法。我们证明,NaCl型和WC型TMCs的本征硬度分别在每个晶胞约9个和10.25个价电子浓度时达到最大值;任何偏离这些最佳值的情况都会降低硬度。使用放电等离子烧结技术,成功合成了多种WReC(x = 0 - 0.5),粉末X射线衍射表明它们采用六方WC型结构。随后的纳米压痕和维氏硬度测量证实,新开发的WReC样品(x = 0.1 - 0.3)比其母相(即WC)硬得多,使其成为实际应用中最硬的TMCs。此外,硬度的提高可以通过成键态和反键态的平衡占据得到很好的解释。我们的发现不仅阐明了一大类TMCs中独特的硬化机制,还为设计其他硬质和超硬化合物(如硼化物和氮化物)提供了指导。

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