journal article·2016-06-22Open access

Mechanistic Study of the Conversion of Superoxide to Oxygen and Hydrogen Peroxide in Carbon Nanoparticles

Almaz S. Jalilov, Chenhao Zhang, Errol L. G. Samuel, William K. A. Sikkema, Gang Wu, Vladimir Berka, Thomas A. Kent, Ah-Lim Tsai, James M. Tour

Abstract

Hydrophilic carbon clusters (HCCs) are oxidized carbon nanoparticles with a high affinity for electrons. The electron accepting strength of HCCs, employing the efficient conversion of superoxide (O2(•-)) to molecular oxygen (O2) via single-electron oxidation, was monitored using cyclic voltammetry and electron paramagnetic resonance spectroscopy. We found that HCCs possess O2 reduction reaction (ORR) capabilities through a two-electron process with the formation of H2O2. By comparing results from aprotic solvents to those obtained from ORR activity in aqueous media, we propose a mechanism for the origin of the antioxidant and superoxide dismutase mimetic properties of poly(ethylene glycolated) hydrophilic carbon clusters (PEG-HCCs).
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Research context

OpenAlex topics: Carbon Nanotubes in Composites · Electrochemical sensors and biosensors · Catalytic Processes in Materials Science

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Affiliations

Hematology, Department of Internal Medicine, University of Texas Houston Medical School, Houston, Texas 77030, United States

Funding

John S. Dunn Foundation · National Institute of Neurological Disorders and Stroke

References (41)

Show source-provided references
1. 10.1016/0002-9343(91)90279-710.1016/0002-9343(91)90279-7 ↗
2. 10.1016/S1367-5931(98)80067-710.1016/S1367-5931(98)80067-7 ↗
3. Bandyopadhyay U. · Curr. Sci. · 1999 · 77 · 658
4. 10.1038/nchembio.60710.1038/nchembio.607 ↗
5. 10.1016/j.cbpa.2004.02.01110.1016/j.cbpa.2004.02.011 ↗
6. 10.1016/S0168-1656(97)01677-510.1016/S0168-1656(97)01677-5 ↗
7. 10.1007/s00018-003-3206-510.1007/s00018-003-3206-5 ↗
8. 10.1021/cr900302x10.1021/cr900302x ↗
9. 10.1021/cr500226n10.1021/cr500226n ↗
10. 10.1021/ac960626110.1021/ac9606261 ↗
11. Zhang X. · 2008
12. Zhang, J.PEM Fuel Cell Electrocatalysts and Catalyst Layers: Fundamentals and Applications;Springer-Verlag London Ltd:London, U.K., 2008; Chapter 2, pp89–135.10.1007/978-1-84800-936-3 ↗
13. 10.1039/c3ee43385d10.1039/c3ee43385d ↗
14. 10.1021/cr500356310.1021/cr5003563 ↗
15. Boulatov R. · 2009 · 63710.1002/9780470463772.ch18 ↗
16. 10.1134/S102319350709012110.1134/S1023193507090121 ↗
17. 10.1021/ic00005a05110.1021/ic00005a051 ↗
18. 10.1021/ja063283p10.1021/ja063283p ↗
19. 10.1021/ja805721p10.1021/ja805721p ↗
20. 10.1021/nn100975c10.1021/nn100975c ↗
21. 10.1021/nn204885f10.1021/nn204885f ↗
22. 10.1021/nn302615f10.1021/nn302615f ↗
23. 10.1016/j.tibtech.2014.08.00510.1016/j.tibtech.2014.08.005 ↗
24. 10.1021/cm503750210.1021/cm5037502 ↗
25. 10.1021/nn504637y10.1021/nn504637y ↗
26. 10.1002/adma.20120232110.1002/adma.201202321 ↗
27. 10.1073/pnas.141704711210.1073/pnas.1417047112 ↗
28. 10.1021/ar00072a00510.1021/ar00072a005 ↗
29. 10.1021/ar700256a10.1021/ar700256a ↗
30. 10.1073/pnas.16209559910.1073/pnas.162095599 ↗
31. 10.1021/nn100636810.1021/nn1006368 ↗
32. 10.1002/chem.20130188910.1002/chem.201301889 ↗
33. 10.1002/cber.1898031023710.1002/cber.18980310237 ↗
34. 10.1002/zaac.1937234040510.1002/zaac.19372340405 ↗
35. 10.1021/ja01539a01710.1021/ja01539a017 ↗
36. 10.1021/jp111941s10.1021/jp111941s ↗
37. 10.1016/j.carbon.2011.04.04710.1016/j.carbon.2011.04.047 ↗
38. Sawyer D. T. · 1991
39. 10.1021/ja053911n10.1021/ja053911n ↗
40. 10.1021/ac101854w10.1021/ac101854w ↗
41. 10.1002/1521-4109(200202)14:3<165::AID-ELAN165>3.0.CO;2-610.1002/1521-4109(200202)14:3<165::AID-ELAN165>3.0.CO;2-6 ↗