Department of Chemistry and Biochemistry , University of California , Santa Cruz , California 95064 , United States.
Chemical Sciences Division, Joint Center for Artificial Photosynthesis , Lawrence Berkeley National Laboratory , Berkeley , California 94720 , United States.
ACS Appl Mater Interfaces. 2018 Apr 18;10(15):12992-13001. doi: 10.1021/acsami.8b00726. Epub 2018 Apr 6.
In principle, the diameter and surface plasmon resonance (SPR) frequency of hollow metal nanostructures can be independently adjusted, allowing the formation of targeted photoactivated structures of specific size and optical functionality. Although tunable SPRs have been reported for various systems, the shift in SPR is usually concomitant with a change in particle size. As such, more advanced tunability, including constant diameter with varying SPR or constant SPR with varying diameter, has not been properly achieved experimentally. Herein, we demonstrate this advanced tunability with hollow gold nanospheres (HGNs). HGNs were synthesized through galvanic exchange using cobalt-based nanoparticles (NPs) as sacrificial scaffolds. CoB NP scaffolds were prepared by sodium borohydride nucleation of aqueous cobalt chloride and characterized using UV-vis, dynamic light scattering, X-ray absorption spectroscopy, and X-ray photoelectron spectroscopy. Careful control over the size of the CoB scaffold and its galvanic conversion is essential to realize fine control of the resultant HGN diameter and shell thickness. In pursuit of size control, we introduce B(OH) (the final product of NaBH hydrolysis) as a growth agent to obtain hydrodynamic diameters ranging from ∼17-85 nm with relative standard deviation <3%. The highly monodisperse CoB NPs were then used as scaffolds for the formation of HGNs. In controlling HGN shell thickness and uniformity, environmental oxygen was shown to affect both the structural and optical properties of the resultant gold shells. With careful control of these key factors, we demonstrate an HGN synthesis that enables independent variation of diameter and shell thickness, and thereby SPR, with unprecedented uniformity. The new synthesis method creates a truly tunable plasmonic nanostructure platform highly desirable for a wide range of applications, including sensing, catalysis, and photothermal therapy.
原则上,空心金属纳米结构的直径和表面等离子体共振(SPR)频率可以独立调节,从而可以形成具有特定尺寸和光学功能的目标光激活结构。尽管已经报道了各种系统的可调谐 SPR,但 SPR 的位移通常伴随着颗粒尺寸的变化。因此,尚未在实验上实现更先进的可调性,包括具有变化的 SPR 的恒定直径或具有变化的直径的恒定 SPR。在此,我们使用空心金纳米球(HGN)证明了这种先进的可调性。通过使用钴基纳米颗粒(NPs)作为牺牲支架的电置换来合成 HGN。CoB NP 支架通过水相氯化钴的硼氢化钠成核制备,并通过紫外可见光谱,动态光散射,X 射线吸收光谱和 X 射线光电子能谱进行了表征。仔细控制 CoB 支架的尺寸及其电置换对于实现所得 HGN 直径和壳层厚度的精细控制至关重要。为了实现尺寸控制,我们引入了 B(OH)(NaBH 水解的最终产物)作为生长剂,以获得范围从∼17-85nm 的水动力直径,相对标准偏差<3%。然后,将高度单分散的 CoB NPs 用作形成 HGN 的支架。在控制 HGN 壳层厚度和均匀性时,环境氧显示出对所得金壳的结构和光学性质都有影响。通过仔细控制这些关键因素,我们展示了一种 HGN 合成方法,该方法可实现前所未有的均匀性,从而实现独立变化的直径和壳层厚度以及 SPR。这种新的合成方法创建了一个真正可调谐的等离子体纳米结构平台,非常适合各种应用,包括传感,催化和光热疗法。