Polypyrrole-assisted oxygen electrocatalysis on perovskite oxides

Citation data:

Energy & Environmental Science, ISSN: 1754-5692, Vol: 10, Issue: 2, Page: 523-527

Publication Year:
2017
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Repository URL:
http://scholarworks.unist.ac.kr/handle/201301/21156
DOI:
10.1039/c6ee03501a
Author(s):
Lee, Dong-Gyu, Kim, Su Hwan, Joo, Se Hun, Ji, Ho-Il, Tavassol, Hadi, Jeon, Yuju, Choi, Suhyuk, Lee, Myeing-Hee, Kim, Chanseok, Kwak, Sang Kyu, Kim, Guntae, Song, Hyun-Kon Show More Hide
Publisher(s):
Royal Society of Chemistry (RSC), The Royal Society of Chemistry, ROYAL SOC CHEMISTRY
Tags:
Environmental Science, Energy
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article description
Nitrogen-containing electrocatalysts, such as metal-nitrogen-carbon (M-N-C) composites and nitrogen-doped carbons, are known to exhibit high activities for an oxygen reduction reaction (ORR). Moreover, even if the mechanism by which nitrogen improves the activities is not completely understood, a strong electronic interaction between nitrogen and active sites has been found in these composites. Herein, we demonstrate a case in which nitrogen improves the electroactivity, but in the absence of a strong interaction with other components. The overpotentials of the ORR and oxygen evolution reaction (OER) on perovskite oxide catalysts were significantly reduced simply by mixing the catalyst particles with polypyrrole/carbon composites (pPy/C). Any strong interactions between pPy (a nitrogen-containing compound) and active sites of the catalysts are not confirmed. A scenario based on the sequential task allocation between pPy and oxide catalysts for the ORR was proposed: (1) molecular oxygen is incorporated into pPy as a form of superoxide (pPyO), (2) the superoxide is transferred to the active sites of perovskite catalysts, and (3) the superoxide is completely reduced along the 4e ORR process.

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