小角X射线散射
材料科学
纳米线
双层
层状结构
透射电子显微镜
纳米技术
纳米结构
自组装
纳米颗粒
堆积
肺表面活性物质
散射
结晶学
化学工程
膜
复合材料
光学
有机化学
化学
物理
工程类
生物
遗传学
作者
Scott C. McGuire,Yugang Zhang,Stanislaus S. Wong
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2022-08-31
卷期号:33 (47): 475602-475602
标识
DOI:10.1088/1361-6528/ac893b
摘要
Abstract Ultrathin Pt nanowires possess high activity for various electrocatalytic applications. However, little work has focused on understanding their growth mechanisms. Herein, we utilize a combination of time-dependent, ex situ transmission electron microscopy (TEM) and small angle x-ray scattering (SAXS) techniques to observe the growth process in addition to associated surfactant-based interactions. TEM images indicate that initially nanoparticles are formed within 30 s; these small ‘seed’ particles quickly elongate to form ultrathin nanowires after 2 min. These motifs remain relatively unchanged in size and shape up to 480 min of reaction. Complementary SAXS data suggests that the initial nanoparticles, which are coated by a surfactant bilayer, arrange into a bcc superlattice. With increasing reaction time, the bcc lattice disappears as the nanoparticles grow into nanowires, which then self-assemble into a columnar hexagonal structure in which the individual nanowires are covered by a CTAB monolayer. The hexagonal structure eventually degrades, thereby leading to the formation of lamellar stacking phases comprised of surfactant bilayers. To the best of our knowledge, this is the first time that SAXS has been used to monitor the growth and self-assembly of Pt nanowires. These insights can be used to better understand and rationally control the formation of anisotropic motifs of other metallic nanostructures.
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