Utilizing in Situ Electrochemical SHINERS for Oxygen Reduction Reaction Studies in Aprotic Electrolytes
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...
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Published in | The journal of physical chemistry letters Vol. 7; no. 11; pp. 2119 - 2124 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
02.06.2016
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Online Access | Get full text |
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Summary: | 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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1948-7185 1948-7185 |
DOI: | 10.1021/acs.jpclett.6b00730 |