Abstract

We studied the near-field properties of localized surface plasmon resonances in finite linear gold nanochains using photoemission electron microscopy (PEEM). The localization of the electromagnetic field in the near-field region was mapped at high spatial resolution. By tuning the excitation laser wavelength, we can obtain the near-field spectra, from which the energy splitting between longitudinal (L) and transverse (T) plasmon modes can be revealed. In particular, the L-mode red shifts and the T-mode blue shifts with increasing chain length. The red shift of the L-mode is highly dependent on the gap distance. In contrast, the T-mode almost remains constant within the range of gap distance we investigated. This energy splitting between the L-mode and the T-mode of metallic chains is in agreement with previous far-field measurements, where it was explained by dipole-dipole near-field coupling. Here, we provide direct proof of this near-field plasmon coupling in nanochains via the above-described near-field measurements using PEEM. In addition, we explore the energy transport along the gold nanochains under excitation at oblique illumination via PEEM measurements together with numerical simulations.

Highlights

  • Metallic nanoparticles exhibit localized surface plasmon resonances (LSPRs) associated with the local field enhancement around the surface of the nanoparticles

  • 1-D metallic nanoparticle chains has shown that two LSPR modes exist, namely the longitudinal mode (L-mode) and the transverse mode (T-mode), with the polarization of the excitation light parallel and perpendicular to the chain axis, respectively

  • Previous studies based on far-field measurements and/or numerical simulations have shown that the energy splitting between the L-mode and the T-mode is mostly due to near-field coupling[1,13,17]

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Summary

Introduction

Metallic nanoparticles exhibit localized surface plasmon resonances (LSPRs) associated with the local field enhancement (often referred to “hot spots”) around the surface of the nanoparticles. We report experimental studies on the LSPR of finite 1-D gold nanoparticle chains via PEEM using near infrared femtosecond laser pulses as the excitation source.

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