Pang Jie, Liu Hai-Ling, Li Jian, Zhai Ting-Ting, Wang Kang, Xia Xing-Hua
State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry & Chemical Engineering, Nanjing University, Nanjing, 210023, China.
Chemphyschem. 2018 Apr 17;19(8):954-958. doi: 10.1002/cphc.201701148. Epub 2018 Feb 21.
Silver nanoparticles (AgNPs) have been widely used as photocatalysts and nanosensors. Observation of the spectroscopy of a single AgNP greatly helps us understand the catalytic characteristics and morphology change of the AgNP during reactions. In the present study, AgNPs physically adsorbed on indium tin oxide (ITO) conductive glass were electrochemically reduced and oxidized, and the plasmonic resonance Rayleigh scattering (PRRS) spectrum of an individual AgNP was observed under a dark-field microscopy (DFM) equipped with a spectrometer. The electrochemical oxidization of the AgNP under constant potential caused a redshift of the PRRS peak for 30±5 nm. However, electrochemical reduction of the AgNP could not make the PRRS peak completely shift back to the initial position. In situ AFM and SEM characterization confirmed that very small Ag fragments (<10 nm) formed around the AgNP core during electrochemical oxidization. Results showed that dark-field microspectroscopy could be used as a sensitive tool for estimating the morphology/structural changes of nanoparticles that can hardly be observed through the cyclic voltammograms of multiple AgNPs.
银纳米颗粒(AgNPs)已被广泛用作光催化剂和纳米传感器。对单个AgNP的光谱观察极大地有助于我们了解AgNP在反应过程中的催化特性和形态变化。在本研究中,将物理吸附在氧化铟锡(ITO)导电玻璃上的AgNPs进行电化学还原和氧化,并在配备光谱仪的暗场显微镜(DFM)下观察单个AgNP的等离子体共振瑞利散射(PRRS)光谱。在恒电位下AgNP的电化学氧化导致PRRS峰发生30±5 nm的红移。然而,AgNP的电化学还原不能使PRRS峰完全回到初始位置。原位原子力显微镜(AFM)和扫描电子显微镜(SEM)表征证实,在电化学氧化过程中,AgNP核周围形成了非常小的Ag碎片(<10 nm)。结果表明,暗场显微光谱可作为一种灵敏的工具,用于估计通过多个AgNP的循环伏安图难以观察到的纳米颗粒的形态/结构变化。