杰纳斯
纳米技术
纳米颗粒
范德瓦尔斯力
自组装
材料科学
纳米结构
金属有机骨架
连接器
杰纳斯粒子
化学工程
拉曼散射
拉曼光谱
分子
化学
计算机科学
物理
光学
有机化学
操作系统
作者
Huicheng Hu,Fei Ji,Yong Xu,Jiaqi Yu,Qipeng Liu,Lei Chen,Qian Chen,Peng Wen,Y. Lifshitz,Yan Wang,Qiao Zhang,Shuit Tong Lee
出处
期刊:ACS Nano
[American Chemical Society]
日期:2016-07-14
卷期号:10 (8): 7323-7330
被引量:91
标识
DOI:10.1021/acsnano.6b03396
摘要
Reversible self-assembly of nanoparticles into ordered structures is essential for both fundamental study and practical applications. Although extensive work has been conducted, the demand for simple, cheap, reversible, and versatile ordering methods is still a central issue in current nanoscience and nanotechnology. Here we report a reversible and precise self-assembly of nanoparticles through a linker-free and fast approach by manipulating the interparticle forces, e.g., van der Waals (VDW) force and electrostatic force. Because VDW force is nondirectional, an oriented interaction is achieved to induce the directional binding of nanoparticles utilizing the Janus nanostructure. An effective sol–gel approach has been developed to synthesize metal-organosilica Janus nanoparticles. Dimers and trimers can be obtained by tuning the steric hindrance. After assembly, “hot-spots” can be generated between adjacent nanoparticles, and dramatic enhancement has been observed in surface-enhanced Raman scattering. The present strategy overcomes several limitations of existing approaches and allows the controlled assembly of small particles into various structures.
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