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Effect of oxygen plasma treatment on the electrochemical performance of the rayon and polyacrylonitrile based carbon felt for the vanadium redox flow battery application
被引:128
作者:

Dixon, D.
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Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Babu, D. J.
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Tech Univ Darmstadt, Fachbereich Chem, Eduard Zintl Inst Anorgan & Phys Chem, Alarich Weiss Str 12, D-64287 Darmstadt, Germany Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Langner, J.
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Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Bruns, M.
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Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Pfaffmann, L.
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Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Bhaskar, A.
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Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
HIU, Electrochem Energy Storage, POB 3640, D-76021 Karlsruhe, Germany Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Schneider, J. J.
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Tech Univ Darmstadt, Fachbereich Chem, Eduard Zintl Inst Anorgan & Phys Chem, Alarich Weiss Str 12, D-64287 Darmstadt, Germany Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Scheiba, F.
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Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Ehrenberg, H.
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Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
机构:
[1] Karlsruhe Inst Technol, IAM ESS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
[2] Tech Univ Darmstadt, Fachbereich Chem, Eduard Zintl Inst Anorgan & Phys Chem, Alarich Weiss Str 12, D-64287 Darmstadt, Germany
[3] HIU, Electrochem Energy Storage, POB 3640, D-76021 Karlsruhe, Germany
关键词:
Vanadium redox flow batteries;
Oxygen plasma treatment;
PAN felts;
Rayon felts;
Oxygen functional groups;
GRAPHITE FELT;
FUNCTIONAL-GROUPS;
ELECTRODE;
CELL;
OXIDATION;
FIBER;
D O I:
10.1016/j.jpowsour.2016.09.070
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Oxygen plasma treatment was applied on commercially available graphite felt electrodes based on rayon (GFA) and polyacrylonitrile (GFD). The formation of functional groups on the surface of the felt was confirmed by X-ray photoelectron spectroscopy measurements. The BET studies of the plasma treated electrodes showed no significant increase in surface area for both the rayon as well as the PAN based felts. Both plasma treated electrodes showed significantly enhanced V3+/V2+ redox activity compared to the pristine electrodes. Since an increase of the surface area has been ruled out for plasma treated electrode the enhanced activity could be attributed to surface functional groups. Interestingly, plasma treated GFD felts showed less electrochemical activity towards V5+/V4+ compared to the pristine electrode. Nevertheless, an overall increase of the single cell performance was still observed as the negative electrode is known to be the performance limiting electrode. Thus, to a great extent the present work helps to preferentially understand the importance of functional groups on the electrochemical activity of negative and positive redox reaction. The study emphasizes the need of highly active electrodes especially at the negative electrode side as inactive electrodes can still facilitate hydrogen evolution and degrade the electrolyte in VRFBs. (C) 2016 Elsevier B.V. All rights reserved.
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页码:240 / 248
页数:9
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