Utilizing in Situ Electrochemical SHINERS for Oxygen Reduction Reaction Studies in Aprotic Electrolytes
Author(s) -
Thomas A. Galloway,
Laurence J. Hardwick
Publication year - 2016
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.6b00730
Subject(s) - electrochemistry , electrolyte , raman spectroscopy , electrode , glassy carbon , platinum , chemistry , inorganic chemistry , surface enhanced raman spectroscopy , oxygen , redox , materials science , nanotechnology , catalysis , cyclic voltammetry , raman scattering , organic chemistry , physics , optics
Spectroscopic detection of reaction intermediates upon a variety of electrode surfaces is of major interest within physical chemistry. A notable technique in the study of the electrochemical interface has been surface-enhanced Raman spectroscopy (SERS). The drawback of SERS is that it is limited to roughened gold and silver substrates. Herein we report that shell-isolated nanoparticles for enhanced Raman spectroscopy (SHINERS) can overcome the limitations of SERS and has followed the oxygen reduction reaction (ORR), within a nonaqueous electrolyte, on glassy carbon, gold, palladium, and platinum disk electrodes. The work presented demonstrates SHINERS for spectroelectrochemical studies for applied and fundamental electrochemistry in aprotic electrolytes, especially for the understanding and development of future metal-oxygen battery applications. In particular, we highlight that with the addition of Li(+), both the electrode surface and solvent influence the ORR mechanism, which opens up the possibility of tailoring surfaces to produce desired reaction pathways.
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