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偏应力诱导的范德华键合二硫化锆的金属化、层重构与崩塌

Deviatoric stress-induced metallization, layer reconstruction and collapse of van der Waals bonded zirconium disulfide.

作者信息

Yang Linfei, Li Junwei, Zhang Dongzhou, Liu Yuegao, Hu Qingyang

机构信息

Center for High Pressure Science and Technology Advanced Research, 100193, Beijing, China.

School of Materials Science and Engineering, Jingdezhen Ceramic University, Jingdezhen, 333403, Jiangxi, China.

出版信息

Commun Chem. 2024 Jun 22;7(1):141. doi: 10.1038/s42004-024-01223-1.

Abstract

In contrast to two-dimensional (2D) monolayer materials, van der Waals layered transition metal dichalcogenides exhibit rich polymorphism, making them promising candidates for novel superconductor, topological insulators and electrochemical catalysts. Here, we highlight the role of hydrostatic pressure on the evolution of electronic and crystal structures of layered ZrS. Under deviatoric stress, our electrical experiments demonstrate a semiconductor-to-metal transition above 30.2 GPa, while quasi-hydrostatic compression postponed the metallization to 38.9 GPa. Both X-ray diffraction and Raman results reveal structural phase transitions different from those under hydrostatic pressure. Under deviatoric stress, ZrS rearranges the original ZrS octahedra into ZrS cuboids at 5.5 GPa, in which the unique cuboids coordination of Zr atoms is thermodynamically metastable. The structure collapses to a partially disordered phase at 17.4 GPa. These complex phase transitions present the importance of deviatoric stress on the highly tunable electronic properties of ZrS with possible implications for optoelectronic devices.

摘要

与二维(2D)单层材料不同,范德华层状过渡金属二硫属化物表现出丰富的多态性,使其成为新型超导体、拓扑绝缘体和电化学催化剂的有前途的候选材料。在此,我们强调了静水压力对层状ZrS电子结构和晶体结构演变的作用。在偏应力下,我们的电学实验表明在30.2 GPa以上发生半导体到金属的转变,而准静水压缩将金属化推迟到38.9 GPa。X射线衍射和拉曼结果均揭示了与静水压力下不同的结构相变。在偏应力下,ZrS在5.5 GPa时将原始的ZrS八面体重排为ZrS长方体,其中Zr原子独特的长方体配位在热力学上是亚稳的。该结构在17.4 GPa时坍塌为部分无序相。这些复杂的相变表明了偏应力对ZrS高度可调电子性质的重要性,这可能对光电器件有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6c/11193816/6e0f9c7212e5/42004_2024_1223_Fig1_HTML.jpg

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