Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB3 0FS, United Kingdom.
Department of Engineering, University of Cambridge, Trumpington Street, Cambridge, CB2 1PZ, United Kingdom.
J Chem Phys. 2019 Dec 28;151(24):244708. doi: 10.1063/1.5131703.
Plasmonic structures have attracted much interest in science and engineering disciplines, exploring a myriad of potential applications owing to their strong light-matter interactions. Recently, the plasmonic concentration of energy in subwavelength volumes has been used to initiate chemical reactions, for instance by combining plasmonic materials with catalytic metals. In this work, we demonstrate that plasmonic nanoparticles of earth-abundant Mg can undergo galvanic replacement in a nonaqueous solvent to produce decorated structures. This method yields bimetallic architectures where partially oxidized 200-300 nm Mg nanoplates and nanorods support many smaller Au, Ag, Pd, or Fe nanoparticles, with potential for a stepwise process introducing multiple decoration compositions on a single Mg particle. We investigated this mechanism by electron-beam imaging and local composition mapping with energy-dispersive X-ray spectroscopy as well as, at the ensemble level, by inductively coupled plasma mass spectrometry. High-resolution scanning transmission electron microscopy further supported the bimetallic nature of the particles and provided details of the interface geometry, which includes a Mg oxide separation layer between Mg and the other metal. Depending on the composition of the metallic decorations, strong plasmonic optical signals characteristic of plasmon resonances were observed in the bulk with ultraviolet-visible spectrometry and at the single particle level with darkfield scattering. These novel bimetallic and multimetallic designs open up an exciting array of applications where one or multiple plasmonic structures could interact in the near-field of earth-abundant Mg and couple with catalytic nanoparticles for applications in sensing and plasmon-assisted catalysis.
等离子体结构在科学和工程学科中引起了广泛的兴趣,由于其强大的光物质相互作用,探索了许多潜在的应用。最近,亚波长体积中的等离子体能量集中被用于引发化学反应,例如将等离子体材料与催化金属结合。在这项工作中,我们证明了丰富的镁的等离子体纳米粒子可以在非水溶剂中进行电置换,以产生装饰结构。这种方法产生了双金属结构,其中部分氧化的 200-300nm 镁纳米板和纳米棒支撑着许多较小的 Au、Ag、Pd 或 Fe 纳米粒子,有可能在单个 Mg 粒子上逐步引入多种装饰成分。我们通过电子束成像和能量色散 X 射线光谱的局部成分映射以及在整体水平上通过电感耦合等离子体质谱研究了这种机制。高分辨率扫描透射电子显微镜进一步支持了颗粒的双金属性质,并提供了界面几何形状的细节,其中包括 Mg 和其他金属之间的 Mg 氧化物分离层。根据金属装饰的组成,用紫外可见光谱在体相和暗场散射在单粒子水平上观察到具有等离子体共振特征的强等离子体光学信号。这些新颖的双金属和多金属设计开辟了一系列令人兴奋的应用,其中一个或多个等离子体结构可以在丰富的 Mg 的近场中相互作用,并与催化纳米粒子结合,用于传感和等离子体辅助催化应用。