Surface-Enhanced Raman Spectroscopy-Scanning Electrochemical Microscopy: Observation of Real-Time Surface pH Perturbations

被引:13
作者
Hatfield, Kendrich O. [1 ]
Gole, Matthew T. [1 ]
Schorr, Noah B. [1 ,2 ]
Murphy, Catherine J. [1 ]
Rodriguez-Lopez, Joaquin [1 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Sandia Natl Labs, Dept Photovolta & Mat Technol, Albuquerque, NM 87185 USA
基金
美国国家科学基金会;
关键词
IN-SITU; 4-MERCAPTOPYRIDINE; ELECTRODES; SILVER; NANOPARTICLES; ADSORPTION; EVOLUTION; SECM;
D O I
10.1021/acs.analchem.1c00888
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Understanding and controlling chemical dynamics at electrode interfaces is key to electrochemical applications in sensing, electrocatalysis, and energy storage. Here, we introduce colocalized surface-enhanced Raman scattering-scanning electrochemical microscopy (SERS-SECM) as a multimodal tool able to simultaneously probe and affect electrochemical interfaces in real time. As a model system to demonstrate SERS-SECM, we used a self-assembled monolayer of 4-mercaptopyridine (4MPy), a pH sensitive Raman indicator, anchored to silver nanoparticles as a substrate. We modulated the local pH at the surface with chronoamperometry, inducing the hydrogen evolution reaction (HER) at the SECM tip and observed subsequent Raman peak height changes in the 4MPy. We then performed cyclic voltammetry of HER at the SECM tip while measuring SERS spectra every 200 ms to highlight the technique's real-time capabilities. Our results show the capability to sensitively interrogate and trigger chemical/electrochemical dynamic surface phenomena. We hope SERS-SECM will provide insight on the link between heterogeneous and homogeneous reactivity at electrochemical interfaces.
引用
收藏
页码:7792 / 7796
页数:5
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