Xue Xiaozheng, Wang Jianchao, Furlani Edward P
Department of Chemical and Biological Engineering and ‡Department of Electrical Engineering, University at Buffalo SUNY , Buffalo, New York 14260, United States.
ACS Appl Mater Interfaces. 2015 Oct 14;7(40):22515-24. doi: 10.1021/acsami.5b08310. Epub 2015 Sep 30.
A theoretical study is presented of the template-assisted formation of crystalline superstructures of magnetic-dielectric core-shell particles. The templates produce highly localized gradient fields and a corresponding magnetic force that guides the assembly with nanoscale precision in particle placement. The process is studied using two distinct and complementary computational models that predict the dynamics and energy of the particles, respectively. Both mono- and polydisperse colloids are studied, and the analysis demonstrates for the first time that although the particles self-assemble into ordered crystalline superstructures, the particle formation is not unique. There is a Brownian motion-induced degeneracy in the process wherein various distinct, energetically comparable crystalline structures can form for a given template geometry. The models predict the formation of hexagonal close packed (HCP) and face centered cubic (FCC) structures as well as mixed phase structures due to in-plane stacking disorders, which is consistent with experimental observations. The polydisperse particle structures are less uniform than the monodisperse particle structures because of the irregular packing of different-sized particles. A comparison of self-assembly using soft- and hard-magnetic templates is also presented, the former being magnetized in a uniform field. This analysis shows that soft-magnetic templates enable an order-of-magnitude more rapid assembly and much higher spatial resolution in particle placement than their hard-magnetic counterparts. The self-assembly method discussed is versatile and broadly applies to arbitrary template geometries and multilayered and multifunctional mono- and polydisperse core-shell particles that have at least one magnetic component. As such, the method holds potential for the bottom-up fabrication of functional nanostructured materials for a broad range of applications. This work provides unprecedented insight into the assembly process, especially with respect to the viability and potential fundamental limitations of realizing structure-dependent material properties for applications.
本文对磁性 - 电介质核壳颗粒晶体超结构的模板辅助形成进行了理论研究。模板产生高度局部化的梯度场和相应的磁力,该磁力以纳米级精度引导颗粒在放置过程中的组装。使用两种不同但互补的计算模型对该过程进行了研究,这两种模型分别预测了颗粒的动力学和能量。研究了单分散和多分散胶体,分析首次表明,尽管颗粒自组装成有序的晶体超结构,但颗粒的形成并非唯一。在该过程中存在布朗运动引起的简并性,即对于给定的模板几何形状,可以形成各种不同的、能量相当的晶体结构。模型预测了由于面内堆积无序而形成的六方密堆积(HCP)和面心立方(FCC)结构以及混合相结构,这与实验观察结果一致。由于不同尺寸颗粒的不规则堆积,多分散颗粒结构不如单分散颗粒结构均匀。还对使用软磁和硬磁模板的自组装进行了比较,前者在均匀场中被磁化。该分析表明,与硬磁模板相比,软磁模板在颗粒放置方面能够实现快一个数量级的组装速度和更高的空间分辨率。所讨论的自组装方法具有通用性,广泛适用于任意模板几何形状以及具有至少一个磁性组分的多层和多功能单分散和多分散核壳颗粒。因此,该方法在自下而上制造用于广泛应用的功能性纳米结构材料方面具有潜力。这项工作为组装过程提供了前所未有的见解,特别是在实现应用中依赖结构的材料特性的可行性和潜在基本限制方面。