Wang Haifeng, Zhou Xiaoqin, Huang Yunhui, Chen Xin, Jin Chuanhong
Institute of New Energy for Vehicles, School of Materials Science and Engineering, Tongji University Shanghai 201804 China
State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University Hangzhou Zhejiang 310027 China
RSC Adv. 2020 Sep 21;10(57):34781-34787. doi: 10.1039/d0ra05759b. eCollection 2020 Sep 16.
Inter-particle interactions play important roles in controlling the structures, dispersion state and chemo-physical properties of colloidal nanoparticles (NPs) in liquid media. In this work, we prepared palladium (Pd) NPs with an average diameter of ∼4.6 nm inside the liquid cell, and investigated their coupled diffusion and aggregation behaviors through liquid cell transmission electron microscopy (LCTEM). analyzing the interaction energies and forces, we derived the effective working range for repulsive double layer interaction experimentally, a value larger than two times the Debye length, suggesting a different interaction behavior of sub-5 nm NPs from that of colloidal NPs in larger sizes. Our results provide insights for the interactions between colloidal ultrafine nanoparticles in solution and will also shed light on the precisely controlled assembly of colloidal nanocrystals for practical applications.
颗粒间相互作用在控制液体介质中胶体纳米颗粒(NPs)的结构、分散状态和化学物理性质方面起着重要作用。在这项工作中,我们在液体池中制备了平均直径约为4.6 nm的钯(Pd)纳米颗粒,并通过液体池透射电子显微镜(LCTEM)研究了它们的耦合扩散和聚集行为。通过分析相互作用能和力,我们通过实验得出了排斥双层相互作用的有效作用范围,该值大于德拜长度的两倍,这表明5nm以下的纳米颗粒与较大尺寸的胶体纳米颗粒具有不同的相互作用行为。我们的结果为溶液中胶体超细纳米颗粒之间的相互作用提供了见解,也将为胶体纳米晶体在实际应用中的精确控制组装提供启示。