Toward High-Contrast Atomic Force Microscopy-Tip-Enhanced Raman Spectroscopy Imaging: Nanoantenna-Mediated Remote-Excitation on Sharp-Tip Silver Nanowire Probes.
Xuezhi MaYangzhi ZhuNing YuSanggon KimQiushi LiuLeonard AponttiDa XuRuoxue YanMing LiuPublished in: Nano letters (2018)
The tip-enhanced Raman spectroscopy (TERS) imaging technique is designed to provide correlated morphological and chemical information with a nanoscale spatial resolution by utilizing the plasmonic resonance supported by metallic nanostructures at the tip apex of a scanning probe. However, limited by the scattering cross sections of these nanostructures, only a small fraction of the incident light can be coupled to the plasmonic resonance to generate Raman signals. The uncoupled light then directly excites background spectra with a diffraction-limited resolution, which becomes the background noise that often blurs the TERS image. Here, we demonstrate how this problem can be solved by physically separating the light excitation region from the Raman signal generation region on the scanning probe. The remote-excitation TERS (RE-TERS) probe, which can be fabricated with a facile, robust and reproducible method, utilizes silver nanoparticles as nanoantennas to mediate the coupling of free-space excitation light to propagating surface plasmon polaritons (SPPs) in a sharp-tip silver nanowire to excite Raman signals remotely. With this RE-TERS probe, a 10 nm spatial resolution was demonstrated on a single-walled carbon nanotube sample, and the strain distribution in a monolayer molybdenum disulfide (MoS2) was mapped.
Keyphrases
- energy transfer
- raman spectroscopy
- quantum dots
- single molecule
- atomic force microscopy
- living cells
- high resolution
- gold nanoparticles
- room temperature
- carbon nanotubes
- high speed
- silver nanoparticles
- electron microscopy
- cardiovascular disease
- fluorescence imaging
- magnetic resonance
- photodynamic therapy
- fluorescent probe
- health information
- small molecule
- air pollution
- molecular dynamics
- highly efficient
- density functional theory