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Proton Transfer in Perfluorosulfonic Acid Functionalized Carbon Nanotubes

Published online by Cambridge University Press:  01 February 2011

Bradley F Habenicht ,
Stephen J Paddison  and
Mark Tuckerman
Bradley F Habenicht
Affiliation:
[email protected], University of Tennessee, Chemical & Biomolecular Engineering, Knoxville, Tennessee, United States
Stephen J Paddison
Affiliation:
[email protected], University of Tennessee, Chemical & Biomolecular Engineering, Knoxville, Tennessee, United States
Mark Tuckerman
Affiliation:
[email protected], New York, Chemistry, New York, New York, United States
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Abstract

Proton dissociation and transfer are investigated with ab initio molecular dynamics (AIMD) simulations of carbon nanotubes (CNT) functionalized with perfluorosulfonic acid (-CF2SO3H) groups with 3 H2O/–SO3H. The CNT systems were constructed both with and without fluorine atoms covalently bound to the inner walls to determine the effects of the presence of fluorine on proton dissociation, hydration, and stabilization. The results of the AIMD trajectories show that decreasing the separation of sulfonic acid groups increases the propensity for proton dissociation. The simulations also revealed that the dissociated proton was preferentially stabilized as a hydrated hydronium (H3O+) cation in the CNT systems with the fluorine. This feature is attributed to the fluorine atoms providing a localized negative charge that promotes hydrogen bonding of the water molecules coordinated to the central hydronium ion. The hydrated H3O+ ion differed from a traditional Eigen cation (H9O4+) as it donated hydrogen bonds to sulfonate oxygen atoms, as well as water molecules.

Keywords

nanostructureionic conductorsimulation
Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 1269: Symposium FF – Polymer Materials and Membranes for Energy Devices , 2010 , 1269-FF06-07
Copyright
Copyright © Materials Research Society 2010

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References

REFERENCES

1 Kreuer, K. D. J. Membr. Sci. 2001, 185, 29–39.Google Scholar
2 Hamrock, S. J.; Yandrasits, M. A. Polym. Rev. 2006, 46, 219–244.Google Scholar
3 Elliott, J. A.; Paddison, S. J. Phys. Chem. Chem. Phys. 2007, 9, 2602–2618.Google Scholar
4 Paddison, S. J.; Paul, R.; Zawodzinski, T. A. J. Electrochem. Soc. 2000, 147, 617–626.Google Scholar
5 Paddison, S. J.; Paul, R.; Zawodzinski, T. A. J. Chem. Phys. 2001, 115, 7753–7761.Google Scholar
6 Paul, R.; Paddison, S. J. J. Chem. Phys. 2005, 123, 224704.Google Scholar
7 Petersen, M. K.; Voth, G. A. J. Phys. Chem. B 2006, 110, 18594–18600.Google Scholar
8 Devanathan, R.; Venkatnathan, A.; Dupuis, M. J. Phys. Chem. B 2007, 111, 8069–8079.Google Scholar
9 Devanathan, R.; Venkatnathan, A.; Dupuis, M. J. Phys. Chem. B 2007, 111, 13006–13013.Google Scholar
10 Hristov, I. H.; Paddison, S. J.; Paul, R. J. Phys. Chem. B 2008, 112, 2937–2949.Google Scholar
11 Eikerling, M.; Paddison, S. J.; Pratt, L. R.; Zawodzinski, T. A. Chem. Phys. Lett. 2003, 368, 108–114.Google Scholar
12 Hayes, R. L.; Paddison, S. J.; Tuckerman, M. E. J. Phys. Chem. B 2009, 113, 16574–16589.Google Scholar
13 Kresse, G.; Hafner, , J. Phys. Rev. B 1993, 47, 558–561.Google Scholar
14 Kresse, G.; Furthmuller, , J. Phys. Rev. B 1996, 54, 11169–11186.Google Scholar
15 Perdew, J. P.; Burke, K.; Ernzerhof, M. Phys. Rev. Lett. 1996, 77, 3865–3868.Google Scholar
16 Blochl, P. E. Phys. Rev. B 1994, 50, 17953–17979.Google Scholar
17 Kresse, G.; Joubert, D. Phys. Rev. B 1999, 59, 1758–1775.Google Scholar
18 Kent, P. R. C. J. Phys. Conf. Ser. 2008, 012058.Google Scholar
19www.nics.tennessee.eduGoogle Scholar
20 Marx, D.; Tuckerman, M. E.; Hutter, J.; Parrinello, M. Nature 1999, 397, 601–604.Google Scholar
21 Ojamae, L.; Shavitt, I.; Singer, S. J. Int. J. Quantum Chem. 1995, Suppl. 29, 657–668.Google Scholar