Li Qian, Cheng Hongfei, Xing Caihong, Guo Songhao, Wu Xiaotong, Zhang Liming, Zhang Dongzhou, Liu Xingchen, Wen Xiaodong, Lü Xujie, Zhang Hua, Quan Zewei
Department of Chemistry, Academy for Advanced Interdisciplinary Studies, Shenzhen Engineering Research Center for Frontier Materials Synthesis at High Pressures, Southern University of Science and Technology (SUSTech), Shenzhen, Guangdong, 518055, China.
Center for Programmable Materials, School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore, 639798, Singapore.
Small. 2022 Apr;18(17):e2106396. doi: 10.1002/smll.202106396. Epub 2022 Mar 28.
Control of structural ordering in noble metals is very important for the exploration of their properties and applications, and thus it is highly desired to have an in-depth understanding of their structural transitions. Herein, through high-pressure treatment, the mutual transformations between crystalline and amorphous phases are achieved in Pd nanosheets (NSs) and nanoparticles (NPs). The amorphous domains in the amorphous/crystalline Pd NSs exhibit pressure-induced crystallization (PIC) phenomenon, which is considered as the preferred structural response of amorphous Pd under high pressure. On the contrary, in the spherical crystalline@amorphous core-shell Pd NPs, pressure-induced amorphization (PIA) is observed in the crystalline core, in which the amorphous-crystalline phase boundary acts as the initiation site for the collapse of crystalline structure. The distinct PIC and PIA phenomena in two different heterophase Pd nanostructures might originate from the different characteristics of Pd NSs and NPs, including morphology, amorphous-crystalline interface, and lattice parameter. This work not only provides insights into the phase transition mechanisms of amorphous/crystalline heterophase noble metal nanostructures, but also offers an alternative route for engineering noble metals with different phases.
控制贵金属中的结构有序性对于探索其性质和应用非常重要,因此非常希望深入了解其结构转变。在此,通过高压处理,在钯纳米片(NSs)和纳米颗粒(NPs)中实现了晶相和非晶相之间的相互转变。非晶/晶态钯纳米片中的非晶域表现出压力诱导结晶(PIC)现象,这被认为是高压下非晶钯的首选结构响应。相反,在球形晶态@非晶核壳钯纳米颗粒中,在晶态核中观察到压力诱导非晶化(PIA),其中非晶-晶相界作为晶体结构崩塌的起始位点。两种不同异相钯纳米结构中不同的PIC和PIA现象可能源于钯纳米片和纳米颗粒的不同特性,包括形态、非晶-晶界面和晶格参数。这项工作不仅为非晶/晶态异相贵金属纳米结构的相变机制提供了见解,还为制备具有不同相的贵金属提供了一条替代途径。