Interactions Between Epitaxial Graphene Grown on the Si- and C-Faces of 4H-SiC Investigated Using Raman Imaging and Tip-Enhanced Raman Scattering.

Interactions between epitaxial graphene grown on Si- and C-faces were investigated using Raman imaging and tip-enhanced Raman scattering (TERS). In the TERS spectrum, which has a spatial resolution exceeding the diffraction limit, a D band was observed not from graphene surface, but from the edges of the epitaxial graphene ribbons without a buffer layer, which interacts with SiC on the Si-face. In contrast, for a graphene micro-island on the C-face, the D band disappeared even on the edges where the C atoms were arranged in armchair configurations.

Characterization of SiC-grown epitaxial graphene microislands using tip-enhanced Raman spectroscopy.

Single-layer graphene microislands with smooth edges and no visible grain boundary were epitaxially grown on the C-face of 4H-SiC and then characterized at the nanoscale using tip-enhanced Raman spectroscopy (TERS). Although these graphene islands appear highly homogeneous in micro-Raman imaging, TERS reveals the nanoscale strain variation caused by ridge nanostructures. A G' band position shift up to 9 cm(-1) and a band broadening up to 30 cm(-1) are found in TERS spectra obtained from nanoridges, which is explained by the compressive strain relaxation mechanism.

Anisotropic gold nanoassembly: a study on polarization-dependent and polarization-selective surface-enhanced Raman scattering.

A simple one-step process was adopted to fabricate anisotropic gold nanoassemblies. Evaporation-assisted nanoparticle assembly at the meniscus was maintained in this regard. Scanning electron microscopy confirmed that the constituent nanoparticles of the anisotropic gold nanoassembly are neither in physical contact nor agglomerated; instead, they are separated by a small interparticle gap.

Tip-enhanced Raman spectroscopic measurement of stress change in the local domain of epitaxial graphene on the carbon face of 4H-SiC(000-1).

We develop a bulk silver tip for tip-enhanced Raman scattering (TERS) and obtain TERS spectra of epitaxial graphene on the carbon face of 4H-SiC(000-1) with a high signal-to-noise ratio. Thanks to the high quality of TERS spectra we firstly find that the G band in the TERS spectra exhibits position-by-position variations in both lower wavenumber shifts and spectral broadening. The analysis of the variations reveals that the shifts and broadenings have a linear correlation between each other, indicating that the variations are induced by the position dependent local stress on graphene based on a uniaxial strain model.

Characteristics of surface-enhanced Raman scattering and surface-enhanced fluorescence using a single and a double layer gold nanostructure.

This paper reports the characteristics of surface-enhanced Raman scattering (SERS) and surface-enhanced fluorescence (SEF) using a unique SERS-active substrate comprised of a single layer and a double layer of two-dimensional (2D) gold nanostructure. Colloidal gold nanoparticles were immobilized on a glass substrate and a multi-purpose experimental setup was adopted to obtain surface plasmon resonance (SPR), SERS and SEF on a single platform. Inhomogeneous intensity distribution was observed in correlated images of SPR and SERS.