Dual-template synthesis of ordered mesoporous carbon/Fe2O3 nanowires: high porosity and structural stability for supercapacitors

Junkai Hu, Malachi Noked, Eleanor Gillette, Fudong Han, Zhe Gui, Chunsheng Wang, Sang Bok Lee

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

Carbon/metal oxide composites are considered promising materials for high energy density supercapacitors. So far, impregnation of the oxide into ordered mesoporous carbon materials has been demonstrated either in hard-templated carbon synthesized by using ordered mesoporous silica or alumina scaffolds, or soft-templated carbon derived from surfactant micelles. The hard-template method can provide a high pore volume but the instability of these mesostructures hinders total electrode performances upon oxide impregnation. While the soft-template methods can provide a stable mesostructure, these methods produce scaffolds with a much smaller pore volume and surface area, leading to limited metal oxide loading and electrode capacitance. Herein, anodized aluminum oxide (AAO) and triblock copolymer F127 are used together as hard and soft-templates to fabricate ordered mesoporous carbon nanowires (OMCNWs) as a host material for Fe2O3 nanoparticles. This dual-template strategy provides a high pore volume and surface area OMCNW that retains its stable structure even for high metal oxide loading amounts. Additionally, the unique nanowire morphology and mesoporous structure of the OMCNW/Fe2O3 facilitate high ionic mobility in the composite, leading to >260 F g-1 specific capacitance with good rate capability and cycling stability. This work highlights the dual-template approach as a promising strategy for the fabrication of next generation heterogeneous composites for electrochemical energy storage and conversion.

Original languageEnglish
Pages (from-to)21501-21510
Number of pages10
JournalJournal of Materials Chemistry A
Volume3
Issue number43
DOIs
StatePublished - 9 Oct 2015
Externally publishedYes

Bibliographical note

Publisher Copyright:
© The Royal Society of Chemistry.

Funding

FundersFunder number
Office of ScienceDESC0001160

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