石墨烯
共价键
钻石
异质结
同种类的
材料科学
金刚石材料性能
碳纤维
纳米技术
光电子学
复合材料
复合数
化学
物理
热力学
有机化学
作者
Bin Shen,Zhe Ji,Qiang Lin,Peng Gong,Ningning Xuan,Sulin Chen,Hanqi Liu,Zhewei Huang,Taishi Xiao,Zhengzong Sun
标识
DOI:10.1021/acs.chemmater.1c04322
摘要
Diamond and graphene are the most well-studied allotropes of carbon. Both are superior in mechanical, optical, and electrical properties yet are rarely used together in combined forms. People have reported graphene–diamond heterostructures connected by van der Walls forces. However, a hybrid graphene–diamond heterostructure connected by covalent bonds would be much more robust to tackle demanding challenges such as ultrahard material machining and high-power diamond electronics. Here, we demonstrate a method of direct catalytic graphenization of diamond. Homogeneous graphene–diamond heterostructures, featured with covalent bonded interfaces, were indiscriminately grown on all diamond facets. The synthesized sp2 graphene (0001) sheets seamlessly extend from the diamond (111) sp3 lattice. Such a unique covalent-bond atomic structure gives rise to an unprecedented interfacial bonding strength of ∼150 GPa, surpassing the intrinsic strength of graphene.
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