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CoFe2O4 surface modification with conducting polypyrrole: employed as a highly active electrocatalyst for oxygen evolution reaction
Electrochemical water splitting could be a potentially viable technique for obtaining the energy from renewable sources. The considerable overpotential demanded for sluggish oxygen evolution reaction (OER), however, prevents broad adoption of this approach. Herein, CoFe 2 O 4 /PPY hybrid is synthesi...
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Published in: | Journal of materials science. Materials in electronics 2022-06, Vol.33 (16), p.13244-13254 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Electrochemical water splitting could be a potentially viable technique for obtaining the energy from renewable sources. The considerable overpotential demanded for sluggish oxygen evolution reaction (OER), however, prevents broad adoption of this approach. Herein, CoFe
2
O
4
/PPY hybrid is synthesized with a polypyrrole layered on the top of the CoFe
2
O
4
via facile hydrothermal treatment. CoFe
2
O
4
/PPY is a highly efficient electrocatalyst, because it outperforms than pure CoFe
2
O
4
, PPY in terms of OER. CoFe
2
O
4
/PPY OER activities are comparable to those of commercial electrocatalysts. It's worth noting that the CoFe
2
O
4
/PPY hybrid is significantly more stable than the individuals, due to surface coated with PPY, responsible for good conduction of fast-moving electrons. The CoFe
2
O
4
/PPY coupling increases the OER by promoting electron exchange between the PPY layer and the CoFe
2
O
4
reducing the over potential of (274 mV) and also lower the Tafel slope (47 mV/dec) with lower charge transfer resistance (3.15 Ω). According to the findings, on the top of CoFe
2
O
4
, a layer of PPY is applied for the surface modification using a conducting polymer can improve spinel oxides activity for future applications such as photoelectrocatalytic study, for stabilizing the material activity, etc. |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-022-08265-y |