材料科学
原位
航程(航空)
相变
相(物质)
短期订单
纳米技术
化学工程
冶金
结晶学
凝聚态物理
复合材料
气象学
有机化学
物理
化学
工程类
作者
Shu Fu,Sinan Liu,Jiacheng Ge,Junjie Wang,Huiqiang Ying,Shangshu Wu,Mengyang Yan,Li Zhu,Yubin Ke,Junhua Luan,Yang Ren,Xiaobing Zuo,Zhenduo Wu,Zhen Peng,Chang Liu,Xun-Li Wang,Tao Feng,Si Lan
标识
DOI:10.1016/j.jmst.2022.01.038
摘要
• Bulk-sized nanostructured glasses that exceed millimeters have been prepared. • Short-range order structure stably remains before and after laser evaporation. • Medium-range order dominates the polyamorphous phase transitions induced by P and T. • Multiscale structures and properties can be tailored based on polyamorphism engineering. Engineering multiscale structural hierarchies in glassy alloys enable a broad spectrum of potential applications. Metallic glasses were born in hierarchical structures from atomic-to-nanometer scales. However, the frozen-in structures in traditional metallic glasses prepared by rapid quenching techniques are challenging to tailor. Here, we show that a Pd 40 Ni 40 P 20 bulk nanostructured glass of polyamorphous interfacial structures was prepared by inert-gas condensation with a laser evaporation source, and its multiscale structures could be engineered. In-situ scattering experiment results reveal polyamorphous phase transitions occurred in the interfacial regions, which are accompanied by the evolution of medium-range order and the nanoscale heterogeneous structures during the condensation process of glassy nanoparticles under high pressure and the following heating process. Moreover, changes in the cluster connectivity resulting from repacking of the local ordering induced by pressure and temperature could be observed. The thermophysical and mechanical properties, including boson peaks, hardness, and elasticity modulus, could be changed as a function of heat-treatment parameters. Our findings would shed light on the synthesis of bulk nanostructured glassy alloys with tailorable thermodynamic and dynamical behavior as well as mechanical properties based on the understanding of metastability for polyamorphous interfacial phases.
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