Journal article
Surface modification of carbon fuels for direct carbon fuel cells
Journal of Power Sources, Vol.186(1), pp.1-9
2009
Abstract
The direct carbon fuel cell (DCFC) is a promising power-generation device that has much higher efficiency (80%) and less emissions than conventional coal-fired power plants. Two commercial carbons (activated carbon and carbon black) pre-treated with HNO3, HCl or air plasma are tested in a DCFC. The correlation between the surface properties and electrochemical performance of the carbon fuels is explored. The HNO3-treated carbon fuels have the highest electrochemical reactivity in the DCFC due to the largest degree of surface oxygen functional groups. The overall effect on changing the electrochemical reactivity of carbon fuels is in the orderHNO3 > air plasma≈HCl. Product gas analysis indicates thatcomplete oxidation of carbon to CO2 can be achieved at 600-700 ◦C.
Details
- Title
- Surface modification of carbon fuels for direct carbon fuel cells
- Authors
- X Li (Author) - University of QueenslandZ Zhu (Author) - University of QueenslandJ Chen (Author) - University of QueenslandRoland De Marco (Author) - Curtin University of TechnologyA Dicks (Author) - University of QueenslandJohn Bradley (Author) - University of QueenslandG Lu (Author) - University of Queensland
- Publication details
- Journal of Power Sources, Vol.186(1), pp.1-9
- Publisher
- Elsevier S.A.
- Date published
- 2009
- DOI
- 10.1016/j.jpowsour.2008.09.070
- ISSN
- 0378-7753
- Copyright note
- Copyright © 2009. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
- Organisation Unit
- University of the Sunshine Coast, Queensland; Office of the Deputy Vice-Chancellor (Research and Innovation)
- Language
- English
- Record Identifier
- 99449746302621
- Output Type
- Journal article
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- Collaboration types
- Domestic collaboration
- Web Of Science research areas
- Chemistry, Physical
- Electrochemistry
- Energy & Fuels
- Materials Science, Multidisciplinary
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