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Strong metal oxide-support interactions in carbon/hematite nanohybrids activate novel energy storage modes for ionic liquid-based supercapacitors

  • Strong metal oxide-support interaction is crucial to activate high energy storage modes of carbon-supported hybrid electrodes in ionic liquid-based supercapacitors. Although it is known that conductive supports can influence the electrochemical properties of metal oxides, insights into how metal oxide-support interactions can be exploited to optimize joint energy storage properties are lacking. We report the junction between alpha-Fe2O3 nanosplotches and phosphorus-doped ordered mesoporous carbon (CMK-3-P) with strong covalent anchoring of the metal oxide. The oxide-carbon interaction in CMK-3-P-Fe2O3 is strengthening the junction and charge transfer between Fe2O3 and CMK-3-P. It enhances energy storage by intensifying the interaction between ionic liquid ions and the surface of the electrode. Density functional theory simulations reveal that the strong metal oxide-support interaction increases the adsorption energy of ionic liquid to -4.77 eV as compared to -3.85 eV for a CMK-3Fe(2)O(3) hybrid with weaker binding. In spite of theStrong metal oxide-support interaction is crucial to activate high energy storage modes of carbon-supported hybrid electrodes in ionic liquid-based supercapacitors. Although it is known that conductive supports can influence the electrochemical properties of metal oxides, insights into how metal oxide-support interactions can be exploited to optimize joint energy storage properties are lacking. We report the junction between alpha-Fe2O3 nanosplotches and phosphorus-doped ordered mesoporous carbon (CMK-3-P) with strong covalent anchoring of the metal oxide. The oxide-carbon interaction in CMK-3-P-Fe2O3 is strengthening the junction and charge transfer between Fe2O3 and CMK-3-P. It enhances energy storage by intensifying the interaction between ionic liquid ions and the surface of the electrode. Density functional theory simulations reveal that the strong metal oxide-support interaction increases the adsorption energy of ionic liquid to -4.77 eV as compared to -3.85 eV for a CMK-3Fe(2)O(3) hybrid with weaker binding. In spite of the lower specific surface area and apparently similar energy storage mode, the CMK-3-P-Fe2O3 exhibits superior electrical double-layer capacitor performance with a specific capacitance of 179 F g(-1) at 2 mV s(-1) (0-3.5 V) in comparison to Fe2O3-free CMK-3 and CMK-3-P reference materials. This principle for design of hybrid electrodes can be applicable for future rational design of stable metal oxide-support electrodes for advanced energy storage.zeige mehrzeige weniger

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Metadaten
Verfasserangaben:Feili LaiORCiD, Jianrui Feng, Tobias Hei, Gui-Chang Wang, Peter Adler, Markus AntoniettiORCiDGND, Martin OschatzORCiDGND
DOI:https://doi.org/10.1016/j.ensm.2019.04.035
ISSN:2405-8297
Titel des übergeordneten Werks (Englisch):Energy Storage Materials
Verlag:Elsevier
Verlagsort:Amsterdam
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Jahr der Erstveröffentlichung:2019
Erscheinungsjahr:2019
Datum der Freischaltung:18.01.2021
Freies Schlagwort / Tag:Ionic liquid; Iron oxide; Main text; Nanohybrid; Ordering transitions; Supercapacitor
Band:20
Seitenanzahl:8
Erste Seite:188
Letzte Seite:195
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
Peer Review:Referiert
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