In situ characterization of surfaces with tip-enhanced Raman spectroscopy (TERS) provides chemical and topographic information with high spatial resolution and submonolayer chemical sensitivity. To further the versatility of the TERS approach toward more complex systems such as biological membranes or energy conversion devices, adaptation of the technique to solid/liquid working conditions is essential. Here, we present a home-built side-illumination TERS setup design based on a commercial scanning tunneling microscope (STM) as a versatile, cost-efficient solution for TERS at solid/liquid interfaces. Interestingly, the results obtained from showcase resonant dye and nonresonant thiophenol monolayers adsorbed on Au single crystals suggest that excitation beam aberrations due to the presence of the aqueous phase are small enough not to limit TER signal detection. The STM parameters are found to play a crucial role for solid/liquid TERS sensitivity. Raman enhancement factors of 10(5) at μW laser power demonstrate the great potential the presented experimental configuration holds for solid/liquid interfacial spectroscopic studies.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.analchem.6b01080DOI Listing

Publication Analysis

Top Keywords

tip-enhanced raman
8
raman spectroscopy
8
solid/liquid interfaces
8
solid/liquid
5
ters
5
versatile side-illumination
4
side-illumination geometry
4
geometry tip-enhanced
4
spectroscopy solid/liquid
4
interfaces situ
4

Similar Publications

Fiber Vector Light-Field-Based Tip-Enhanced Raman Spectroscopy.

Nano Lett

January 2025

Key Laboratory of Light Field Manipulation and Information Acquisition, Ministry of Industry and Information Technology, School of Physical Science and Technology, Northwestern Polytechnical University, Xi'an 710129, China.

Tip-enhanced Raman spectroscopy (TERS) has been extensively employed to investigate the light-matter interaction at the nanoscale. However, the current TERS strategies lack the ability to excite the low-background inhomogeneous electromagnetic field with significant enhancement of electric field, electric field gradient, and optomagnetic field, simultaneously. To overcome this, we developed a fiber vector light-field-based TERS strategy aimed at exploring the multipole Raman scattering processes of molecules.

View Article and Find Full Text PDF

Surface-enhanced Raman spectroscopy: a half-century historical perspective.

Chem Soc Rev

December 2024

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, School of Electronic Science and Engineering, College of Environment and Ecology, State Key Laboratory of Marine Environmental Science, Department of Physics, iChEM, IKKEM, Xiamen University, Xiamen 361005, China.

Surface-enhanced Raman spectroscopy (SERS) has evolved significantly over fifty years into a powerful analytical technique. This review aims to achieve five main goals. (1) Providing a comprehensive history of SERS's discovery, its experimental and theoretical foundations, its connections to advances in nanoscience and plasmonics, and highlighting collective contributions of key pioneers.

View Article and Find Full Text PDF
Article Synopsis
  • The study presents an analytic model that improves the understanding of Raman and fluorescence enhancement in molecules situated between two closely spaced gold nanospheres, taking into account higher-order modes along with the traditional dipolar mode.
  • The model is validated by gap-dependent tip-enhanced Raman spectroscopy (TERS) experiments, which reveal varying trends of photoluminescence and Raman enhancement as the gap width decreases.
  • A red-shift in the background spectra indicates greater coupling between the nanospheres, demonstrating how the model effectively explains the mechanisms at play in the TERS experimental observations.
View Article and Find Full Text PDF

Transition metal dichalcogenide (TMDs) heterostructure, particularly the lateral heterostructure of two different TMDs, is gaining attention as ultrathin photonic devices based on the charge transfer (CT) excitons generated at the junction. However, the characteristics of the interface of the lateral heterostructure, determining the electronic band structure and alignment at the heterojunction region, have rarely been studied due to the limited spatial resolution of nondestructive analysis systems. In this study, we investigated the confined phonons resulting from the phonon-disorder scattering process involving multiple disorders at the lateral heterostructure interface of MoS-WS to prove the consequences of disorder-mediated deformation in the band structure.

View Article and Find Full Text PDF

Real-Space Spectral Determination of Short Single-Stranded DNA Sequence Structures.

J Am Chem Soc

December 2024

Hefei National Research Center for Physical Sciences at the Microscale and CAS Center for Excellence in Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui 230026, China.

Resolving the sequence and structure of flexible biomolecules such as DNA is crucial to understanding their biological mechanisms and functions. Traditional structural biology methods remain challenging for the analysis of small and disordered biomolecules, especially those that are difficult to label or crystallize. Recent development of single-molecule tip-enhanced Raman spectroscopy (TERS) offers a label-free approach to identifying nucleobases in a single DNA chain.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!