采用原位液体池透射电镜技术,在扫描透射电子显微镜(STEM)中,实时观察溶液中金属钯(Pd)在金(Au)纳米颗粒及团簇周围的异质沉积过程。通过对该动态过程的定量分析,结合高分辨透射电子显微镜(HRTEM)对样品进行形貌与结构表征,研究异质沉积的机理。结果表明,电子束辐照下Au-Pd异质结构纳米颗粒的形成存在两种主要机制:第一种机制中,Pd在Au纳米颗粒表面的生长是以岛状沉积开始,随着时间推移,出现Pd岛的结构弛豫和沿着Au颗粒表面的迁移扩展。伴随Pd的不断沉积和弛豫,Au-Pd复合颗粒的外接圆直径表现为震荡生长,而Au表面的Pd覆盖率显示出随时间单调增加的趋势。第二种机制中,由于Pd单体在Au纳米颗粒上的沉积位点有限,使部分被还原的Pd在Au颗粒以外区域进行同质形核与生长形成Pd团簇,之后再与Au颗粒上的Pd岛合并。进一步的结果分析显示,Au颗粒外围的Pd沉积体为多晶结构,由随机取向的Pd纳米晶粒构成。
We report an in sffu liquid cell scanning transmission electron microscopy (STEM) study of the heterogeneous deposition of palladium (Pd) on spherical gold (Au) nanoparticles in solution. The dynamic processes observed here revealed different behaviors of Pd deposition on Au nanoparticles. Under irradiation by an energetic electron beam, Pd was reduced and selectively deposited on Au nanoparticles through the island deposition mode. The deposition processes were accompanied with structural relaxation and surface migration of the Pd islands, and the size of the Au-Pd composite particles showed oscillatory growth behavior. In contrast, the Pd coverage on Au increased monotonically. In addition, we also captured the formation of Pd clusters through homogeneous nucleation and growth, and the subsequent coalescence of Pd clusters with islands on the Au-Pd heterostructures. The associated heterogeneous deposition mechanisms were proposed and quantitatively analyzed. The shapes and structures of the Au-Pd composite particles were characterized by high- resolution transmission electron microscopy (HRTEM), which revealed the deposited Pd on the Au spherical nanoparticles was polycrystalline and contained several Pd crystallites with random orientations. The results presented here will serve as an important reference to understand heterogeneous growth in liquid solutions.