化学
堆积
共价键
热膨胀
负热膨胀
金属
结晶学
衍射
X射线光电子能谱
格子(音乐)
中子衍射
密度泛函理论
凝聚态物理
计算化学
晶体结构
核磁共振
光学
热力学
物理
有机化学
声学
作者
Yili Cao,Weihua Ji,Kun Lin,Huitong Lin,Qiang Li,Chin-Wei Wang,Na Wang,Jinxia Deng,Jun Chen,Xianran Xing
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2021-07-08
卷期号:60 (14): 10095-10099
被引量:3
标识
DOI:10.1021/acs.inorgchem.1c01261
摘要
Zero thermal expansion (ZTE) is an intriguing phenomenon by virtue of its peculiar lack of expansion and contraction with temperature. The achievement of ZTE in a metallic material is a desired but challenging task. Here we report the ZTE behavior of a single-phase metallic VB2 compound, stacking with the V and B atomic layers along the c direction (αV = 2.18 × 10–6 K–1, 5–150 K). Neutron powder diffraction demonstrates that the ZTE behavior is entangled in the direct blocking of the lattice expansion along all crystallographic directions with temperature. X-ray photoelectron spectroscopy and density functional theory calculations indicate that strong covalent binding adheres the nearest-neighbor B–B and V–B pairs, which is proposed to control the ZTE within both the basal plane and the c direction. An intimate correlation is revealed between the covalent binding and the lattice parameters. Our work indicates the opportunity to design metallic ZTE with strong chemical binding in the future.
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