Effects of Cosolvent on the Intermolecular Interactions between an Analyte and a Gold Nanostar Surface Studied Using SERS

Ryan D. Norton; Amanda J. Haes; Alexei V. Tivanski

doi:10.1021/acs.jpcc.4c04360

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Effects of Cosolvent on the Intermolecular Interactions between an Analyte and a Gold Nanostar Surface Studied Using SERS

Journal article

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Effects of Cosolvent on the Intermolecular Interactions between an Analyte and a Gold Nanostar Surface Studied Using SERS

Ryan D. Norton, Amanda J. Haes and Alexei V. Tivanski

Journal of physical chemistry. C, Vol.128(41), pp.17543-17551

10/02/2024

DOI: 10.1021/acs.jpcc.4c04360

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Abstract

For surface-enhanced Raman scattering (SERS), reproducible solution-phase results are typically obtained using nanoparticles functionalized with surface-stabilizing molecules that can prevent the adsorption of analyte molecules with surface affinities lower than those of the stabilizing agent. Herein, we investigate the effects of intermolecular interactions between a nonthiolated analyte and cosolvent to facilitate and modulate analyte adsorption to gold nanostars. SERS, extinction spectroscopy, transmission electron microscopy (TEM), and density functional theory (DFT) calculations are employed in this regard. Tetrahydrofuran (THF) is utilized as a cosolvent in water to facilitate the detection of acetylsalicylic acid (aspirin) on anisotropic gold nanoparticles. Intermolecular interactions between the analyte, solvent, and surface are modulated by changing the solution composition to understand how THF facilitates the SERS detection of aspirin in THF–water cosolvents. SERS signals for 5 mM aspirin arise only in the presence of THF at and above 60 mM, while no signal with or without THF below 60 mM is observed. SERS detection of aspirin is hypothesized to depend on THF forming a hydrogen-bonded complex with aspirin that reduces aspirin hydrophobicity, thus stabilizing the acid form of the molecule and allowing it to weakly interact with the gold nanoparticles. The aspirin–THF complex adsorbs to the gold surface through π-orbital overlap between the aromatic ring and gold, where additional THF weakens orbital overlap. Understanding the mechanism by which organic cosolvents facilitate the SERS detection of nonthiolated analytes such as aspirin, in aqueous media, allows other cosolvents, nonthiolated analytes, and other surfaces to obtain a SERS signal in a variety of systems.

Adsorption

Gold

Oscillation

Raman spectroscopy

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Details

Title: Subtitle: Effects of Cosolvent on the Intermolecular Interactions between an Analyte and a Gold Nanostar Surface Studied Using SERS
Creators: Ryan D. Norton - Department of Chemistry, University of Iowa, Iowa City, Iowa 52242, United States
Amanda J. Haes - Department of Chemistry, University of Iowa, Iowa City, Iowa 52242, United States
Alexei V. Tivanski - University of Iowa, Chemistry
Resource Type: Journal article
Publication Details: Journal of physical chemistry. C, Vol.128(41), pp.17543-17551
Publisher: American Chemical Society
DOI: 10.1021/acs.jpcc.4c04360
ISSN: 1932-7447
eISSN: 1932-7455
Grant note: National Science Foundation (NSF): CHE-2203469
This work was funded by the National Science Foundation (NSF) under the Grant Number CHE-2203469. We thank Peter S. Foley for helpful discussions.
Language: English
Date published: 10/02/2024
Academic Unit: Chemistry
Record Identifier: 9984720725502771

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