Research output: Contribution to journal › Article › peer-review
Bifunctional Oxygen Reduction/Oxygen Evolution Activity of Mixed Fe/Co Oxide Nanoparticles with Variable Fe/Co Ratios Supported on Multiwalled Carbon Nanotubes. / Elumeeva, Karina; Kazakova, Mariya A.; Morales, Dulce Maria et al.
In: ChemSusChem, Vol. 11, No. 7, 09.04.2018, p. 1204-1214.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Bifunctional Oxygen Reduction/Oxygen Evolution Activity of Mixed Fe/Co Oxide Nanoparticles with Variable Fe/Co Ratios Supported on Multiwalled Carbon Nanotubes
AU - Elumeeva, Karina
AU - Kazakova, Mariya A.
AU - Morales, Dulce Maria
AU - Medina, Danea
AU - Selyutin, Alexander
AU - Golubtsov, Georgiy
AU - Ivanov, Yurii
AU - Kuznetzov, Vladimir
AU - Chuvilin, Andrey
AU - Antoni, Hendrik
AU - Muhler, Martin
AU - Schuhmann, Wolfgang
AU - Masa, Justus
N1 - © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2018/4/9
Y1 - 2018/4/9
N2 - A facile strategy is reported for the synthesis of Fe/Co mixed metal oxide nanoparticles supported on, and embedded inside, high purity oxidized multiwalled carbon nanotubes (MWCNTs) of narrow diameter distribution as effective bifunctional catalysts able to reversibly drive the oxygen evolution reaction (OER) and the oxygen reduction reaction (ORR) in alkaline solutions. Variation of the Fe/Co ratio resulted in a pronounced trend in the bifunctional ORR/OER activity. Controlled synthesis and in-depth characterization enabled the identification of an optimal Fe/Co composition, which afforded a low OER/OER reversible overvoltage of only 0.831V, taking the OER at 10mAcm-2 and the ORR at -1mAcm-2. Importantly, the optimal catalyst with a Fe/Co ratio of 2:3 exhibited very promising long-term stability with no evident change in the potential for both the ORR and the OER after 400 charge/discharge (OER/ORR) cycles at 15mAcm-2 in 6m KOH. Moreover, detailed investigation of the structure, size, and phase composition of the mixed Fe/Co oxide nanoparticles, as well as their localization (inside of or on the surface of the MWCNTs) revealed insight of the possible contribution of the individual catalyst components and their synergistic interaction in the catalysis.
AB - A facile strategy is reported for the synthesis of Fe/Co mixed metal oxide nanoparticles supported on, and embedded inside, high purity oxidized multiwalled carbon nanotubes (MWCNTs) of narrow diameter distribution as effective bifunctional catalysts able to reversibly drive the oxygen evolution reaction (OER) and the oxygen reduction reaction (ORR) in alkaline solutions. Variation of the Fe/Co ratio resulted in a pronounced trend in the bifunctional ORR/OER activity. Controlled synthesis and in-depth characterization enabled the identification of an optimal Fe/Co composition, which afforded a low OER/OER reversible overvoltage of only 0.831V, taking the OER at 10mAcm-2 and the ORR at -1mAcm-2. Importantly, the optimal catalyst with a Fe/Co ratio of 2:3 exhibited very promising long-term stability with no evident change in the potential for both the ORR and the OER after 400 charge/discharge (OER/ORR) cycles at 15mAcm-2 in 6m KOH. Moreover, detailed investigation of the structure, size, and phase composition of the mixed Fe/Co oxide nanoparticles, as well as their localization (inside of or on the surface of the MWCNTs) revealed insight of the possible contribution of the individual catalyst components and their synergistic interaction in the catalysis.
KW - Bifunctional catalysts
KW - Fe/Co oxide nanoparticles
KW - Multiwalled carbon nanotubes
KW - Oxygen evolution
KW - Oxygen reduction
KW - multiwalled carbon nanotubes
KW - oxygen evolution
KW - bifunctional catalysts
KW - oxygen reduction
KW - WATER OXIDATION
KW - IRON
KW - ELECTROCATALYSTS
KW - CO OXIDE
KW - COBALT OXIDE
KW - METAL
KW - SPINEL OXIDES
KW - CATALYSTS
KW - IN-SITU
KW - FE
UR - http://www.scopus.com/inward/record.url?scp=85043258207&partnerID=8YFLogxK
U2 - 10.1002/cssc.201702381
DO - 10.1002/cssc.201702381
M3 - Article
C2 - 29359864
AN - SCOPUS:85043258207
VL - 11
SP - 1204
EP - 1214
JO - ChemSusChem
JF - ChemSusChem
SN - 1864-5631
IS - 7
ER -
ID: 12102082