Synthesis and fabrication of nanostructures

Synthesis, fabrication and growth mechanisms of functional nanostructures.

Monodisperse Single-crystal Metal Nanocubes

Metal nanocrystals with special shapes have attracted steadily growing interest due to unique properties and intriguing applications. In most of their potential applications, the quality and the structure of the surface of nanocrystals will undoubtedly play a very important role in determining their functions. Surface-enhanced Raman scattering (SERS) with its high surface sensitivity becomes a powerful technique in studying the optical property of metal nanocystals. Usually, the SERS activity strongly depends on the styles and shapes of metal nanocystals. In the past years, SERS substrate usually is the rough surface, which is difficult to develop the theoretical model based on the experimental data obtained from the ill-defined surfaces because of the heterogeneity in the surface structure. To cope with this difficulty, it is worthwhile to construct the atomic-scale well-defined nanostructure surface which has well-controlled shape, size and space between each other.

Recently, Our group have developed some simple methods in liquid-phase for synthesizing monodisperse single-crystalline Pd, Au, Ag and Au@Pd nanocubes. Noble metal nanocubes exhibit high SERS activity, which are explained by a theoretical calculation using three-dimensional finite difference time domain (FDTD) method. The size- and shape-controlled nanocrystals may be a promising material to bridge the gap between highly rough and single crystal surfaces, and hence allows us to obtain a deep insight into the SERS mechanism and make a mighty advance on understanding and application of nanocrystals.

Growth Mechanisms of Nanocrystals

To extend the shape-controlled growth of nanocrystals, it is highly desirable to develop new synthesis methods and get the deep insight of the growth mechanism. We propose that the exposed crystal faces can be simply tuned by controlling the supersaturation, and higher supersaturation will result in the formation of crystallites with higher surface-energy faces. We have successfully applied it for the growth of ionic (NaCl), molecular (TBPe), and metallic (Au, Pd) micro/nanocrystals with high-surface-energy faces. The above proposed strategy can be rationally designed to synthesize micro/nanocrystals with specific crystal faces and functionality toward specific applications.

Based on the systematic study on the heterogeneous growth mechanism, we have preliminarily proposed a general rule that the atomic radius, bond dissociation energy, and electronegativity of the core and shell metals play key roles in determining the conformal epitaxial layered growth mode. This rule would be help for designing and fabricating more complex nanostructures, such as multiple-shell nanostructures and metal-semiconductor nanocomposites.

The growth of nanoparticles will be affected by the external environment, we found that without centrifugation the Au nanooctahedron seeds grew into truncated octahedrons cuboctahedrons, nanocubes truncated along the [111] and [110] directions, and slightly truncated nanocubes. The mass transfer of Au monomers can be accelerated and the surface reaction step then plays a critical role in shape evolution.

Fabrication of Nanostructures by MEMS method

Nanostructures with gaps in tunneling regime exhibit great research interests because of their widely application in nano-electronics and molecular electronics, and their unique properties in plamonics and catalysis. Mechanically Controllable Break Junction (MCBJ) is an excellent technology to create gap and control the gap distance in tunneling regime precisely and in-situ.

Our group has developed two approaches for the MCBJ method. By using the Microelectromechanical Systems (MEMS) technologies, we firstly fabricate microelectrodes pairs on silicon chips. One of our approach is combining nanoelectrochemistry to electrodeposit interested metals to make the microelectrodes pair form suspended nano-restriction contact. The other one is using Electron-Beam Lithography to fabricate suspended nano-bridge on microelectrodes pair. By bending the chips using a pushing screw underneath, the nanostructures will be broken into nano-electrodes pairs with gaps. With a large reduction ratio, the screw’s sub-micrometer pushing makes gap separation sub-angstrom changes, which means the gap can be controlled precisely in tunneling regime.

The electrodes pair created by MCBJ can be stable, and the break and junction process can be repeated over ten thousands times, whilst the gap can be easily tuned to fit the target molecule length. Thus it is useful to fabricate and measure the electronic properties of Metal Quantum Point Contacts (MQPCs) and Metal-Molecule-Metal (MMM) junctions

As nanostructures show Surface Plasmonic Resonance (SPR) under visible laser illumination. There exists great enhanced electromagnetic field between the gap of nanostructures. By combining Surface-Enhanced Raman Scattering (SERS) technology, we are able to characterize the Raman and electronic properties of molecular junction simultaneously. Besides, as the laser provide a forceful stimuli, the molecular junction in the tunneling regime might also exhibit extraordinary phenomena. By the MCBJ method, the gap distance can be precisely controlled, which can be helpful to measure the nanostructure scattering in-situ, and investigate the relationship between SPR and SERS, even by applying the bias. On the same time, in order to stabilize the molecular junction and eliminate the influence of impurities, and do some low-temperature or temperature-adjustable experiments, we have designed and fabricate a Low-Temperature Ultra-High-Vacuum MCBJ-SERS combined system (LT-UHV-MCBJ-SERS).

References

1. Liu, B.; Xiang, J.; Tian, J.-H.; Zhong, C.; Mao, B.-W.; Yang, F.-Z.; Chen, Z.-B.; Wu, S.-T.; Tian, Z.-Q. Controllable nanogap fabrication on microchip by chronopotentiometry. Electrochimica Acta 50, 3041-3047 (2005).

2. Xiang, J.; Liu, B.; Wu, S. T.; Ren, B.; Yang, F. Z.; Mao, B. W.; Chow, Y. L.; Tian, Z. Q. A Controllable Electrochemical Fabrication of Metallic Electrodes with a Nanometer/Angstrom-Sized Gap Using an Electric Double Layer as Feedback. Angew. Chem. Inter. Edit. 44, 1265-1268 (2005).

3. Tian, J. H.; Liu, B.; Li, X.; Yang, Z. L.; Ren, B.; Wu, S. T.; Tao, N.; Tian, Z. Q. Study of Molecular Junctions with a Combined Surface-Enhanced Raman and Mechanically Controllable Break Junction Method. J. Am. Chem. Soc. 128, 14748-14749 (2006).

4. Tian, J. H.; Yang, Y.; Bo, L.; Schöllhorn, B.; Wu, D. Y.; Maisonhaute, E.; Muns, A. S.; Chen, Y.; Amatore, C.; Tao, N.; Tian, Z. Q. The fabrication and characterization of adjustable nanogaps between gold electrodes on chip for electrical measurement of single molecules. Nanotech. 21, 274012 (2010).

5. Tian, J. H.; Yang, Y.; Zhou, X. S.; Schöllhorn, B.; Maisonhaute, E.; Chen, Z. B.; Yang, F. Z.; Chen, Y.; Amatore, C.; Mao, B. W.; Tian, Z. Q. Electrochemically Assisted Fabrication of Metal Atomic Wires and Molecular Junctions by MCBJ and STM-BJ Methods. ChemPhysChem 11, 2745-2755 (2010).

6. Yang, Y.; Liu, J. Y.; Chen, Z. B.; Tian, J. H.; Jin, X.; Liu, B.; Li, X.; Luo, Z. Z.; Lu, M.; Yang, F. Z.; Tao, N.; Tian, Z. Q. Conductance histogram evolution of an EC–MCBJ fabricated Au atomic point contact. Nanotechnology 22, 275313 (2011).

7. Yang, Y.; Chen, Z. B.; Liu, J. Y.; Lu, M.; Yang, D. Z.; Yang, F. Z.; Tian, Z. Q. An electrochemically assisted mechanically controllable break junction approach for single molecule junction conductance measurements. Nano Research 4, 1199-1207 (2011).


单分散单晶金属纳米立方体

具有特殊形貌的金属纳米晶体由于其独特性质和有趣应用而受到持续增长的关注。在其大多数潜在应用中,纳米晶体表面的质量和结构无疑将在决定其功能方面发挥非常重要的作用。表面增强拉曼散射(SERS)具有很高的表面灵敏度,因而成为研究金属纳米晶体光学性质的有力技术。通常,SERS 活性强烈依赖于金属纳米晶体的类型和形貌。过去几年中,SERS 基底通常是粗糙表面;由于表面结构的非均一性,基于从定义不清表面获得的实验数据建立理论模型十分困难。为解决这一困难,构筑原子尺度上结构明确、形貌、尺寸和相互间距可控的纳米结构表面具有重要价值。

最近,本课题组发展了一些简单的液相方法,用于合成单分散单晶 Pd、Au、Ag 和 Au@Pd 纳米立方体。贵金属纳米立方体表现出高 SERS 活性,并可通过三维有限差分时域(FDTD)方法进行理论计算解释。尺寸和形貌可控的纳米晶体有望成为连接高度粗糙表面与单晶表面的材料,从而帮助我们深入理解 SERS 机理,并显著推动对纳米晶体的认识和应用。

纳米晶体的生长机制

为拓展纳米晶体的形貌可控生长,发展新的合成方法并深入理解生长机制十分重要。我们提出,暴露晶面可以通过控制过饱和度进行简单调控,较高的过饱和度会导致形成具有较高表面能晶面的晶体。我们已将这一策略成功用于具有高表面能晶面的离子型(NaCl)、分子型(TBPe)以及金属型(Au、Pd)微/纳米晶体生长。上述策略可被合理设计,用于合成具有特定晶面和功能、面向特定应用的微/纳米晶体。

基于对异质生长机制的系统研究,我们初步提出了一条通用规律:核金属和壳金属的原子半径、键解离能和电负性在决定共形外延层状生长模式中起关键作用。该规律将有助于设计和制备更复杂的纳米结构,例如多壳层纳米结构和金属-半导体纳米复合物。

纳米粒子的生长会受到外部环境影响。我们发现,在不进行离心的情况下,Au 纳米八面体种子会生长为截角八面体、立方八面体、沿 [111] 和 [110] 方向截角的纳米立方体以及轻微截角的纳米立方体。Au 单体的传质可以被加速,而表面反应步骤随后在形貌演化中发挥关键作用。

利用 MEMS 方法制备纳米结构

具有隧穿尺度间隙的纳米结构因其在纳米电子学和分子电子学中的广泛应用,以及其在等离激元学和催化中的独特性质而具有重要研究价值。机械可控断裂结(MCBJ)是一种优秀技术,可在隧穿尺度创建间隙并精确、原位地控制间隙距离。

本课题组发展了两种 MCBJ 方法。利用微机电系统(MEMS)技术,我们首先在硅芯片上制备微电极对。其中一种方法结合纳米电化学,将目标金属电沉积,使微电极对形成悬空纳米限域接触。另一种方法是利用电子束光刻在微电极对上制备悬空纳米桥。通过芯片下方的推动螺丝弯曲芯片,纳米结构会断裂形成具有间隙的纳米电极对。由于具有很大的缩减比,螺丝的亚微米推动会使间隙分离发生亚埃级变化,这意味着间隙可在隧穿尺度被精确控制。

由 MCBJ 创建的电极对可以保持稳定,断裂和连接过程可重复超过上万次,同时间隙可轻松调节以匹配目标分子的长度。因此,该方法可用于制备并测量金属量子点接触(MQPCs)和金属-分子-金属(MMM)结的电子性质。

纳米结构在可见激光照射下会表现出表面等离激元共振(SPR)。在纳米结构间隙中存在显著增强的电磁场。通过结合表面增强拉曼散射(SERS)技术,我们能够同时表征分子结的拉曼性质和电子性质。此外,由于激光提供了强刺激,处于隧穿尺度的分子结也可能表现出异常现象。通过 MCBJ 方法,间隙距离可以被精确控制,这有助于原位测量纳米结构散射,并研究 SPR 与 SERS 之间的关系,甚至可以在施加偏压的条件下进行研究。同时,为稳定分子结、消除杂质影响,并开展低温或温度可调实验,我们设计并制备了低温超高真空 MCBJ-SERS 联用系统(LT-UHV-MCBJ-SERS)。

参考文献

1. Liu, B.; Xiang, J.; Tian, J.-H.; Zhong, C.; Mao, B.-W.; Yang, F.-Z.; Chen, Z.-B.; Wu, S.-T.; Tian, Z.-Q. Controllable nanogap fabrication on microchip by chronopotentiometry. Electrochimica Acta 50, 3041-3047 (2005).

2. Xiang, J.; Liu, B.; Wu, S. T.; Ren, B.; Yang, F. Z.; Mao, B. W.; Chow, Y. L.; Tian, Z. Q. A Controllable Electrochemical Fabrication of Metallic Electrodes with a Nanometer/Angstrom-Sized Gap Using an Electric Double Layer as Feedback. Angew. Chem. Inter. Edit. 44, 1265-1268 (2005).

3. Tian, J. H.; Liu, B.; Li, X.; Yang, Z. L.; Ren, B.; Wu, S. T.; Tao, N.; Tian, Z. Q. Study of Molecular Junctions with a Combined Surface-Enhanced Raman and Mechanically Controllable Break Junction Method. J. Am. Chem. Soc. 128, 14748-14749 (2006).

4. Tian, J. H.; Yang, Y.; Bo, L.; Schöllhorn, B.; Wu, D. Y.; Maisonhaute, E.; Muns, A. S.; Chen, Y.; Amatore, C.; Tao, N.; Tian, Z. Q. The fabrication and characterization of adjustable nanogaps between gold electrodes on chip for electrical measurement of single molecules. Nanotech. 21, 274012 (2010).

5. Tian, J. H.; Yang, Y.; Zhou, X. S.; Schöllhorn, B.; Maisonhaute, E.; Chen, Z. B.; Yang, F. Z.; Chen, Y.; Amatore, C.; Mao, B. W.; Tian, Z. Q. Electrochemically Assisted Fabrication of Metal Atomic Wires and Molecular Junctions by MCBJ and STM-BJ Methods. ChemPhysChem 11, 2745-2755 (2010).

6. Yang, Y.; Liu, J. Y.; Chen, Z. B.; Tian, J. H.; Jin, X.; Liu, B.; Li, X.; Luo, Z. Z.; Lu, M.; Yang, F. Z.; Tao, N.; Tian, Z. Q. Conductance histogram evolution of an EC–MCBJ fabricated Au atomic point contact. Nanotechnology 22, 275313 (2011).

7. Yang, Y.; Chen, Z. B.; Liu, J. Y.; Lu, M.; Yang, D. Z.; Yang, F. Z.; Tian, Z. Q. An electrochemically assisted mechanically controllable break junction approach for single molecule junction conductance measurements. Nano Research 4, 1199-1207 (2011).