journal article·2014-11-12

Carbon Segregation-Induced Highly Metallic Ni Nanoparticles for Electrocatalytic Oxidation of Hydrazine in Alkaline Media

Tae-Yeol Jeon, Masahiro Watanabe, Kenji Miyatake

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Abstract

The important roles of Ni in electrocatalytic reactions such as hydrazine oxidation are limited largely by high oxidation states because of its intrinsically high oxophilicity. Here, we report the synthesis and properties of highly metallic Ni nanoparticles (NPs) on carbon black supports. We discovered that the heat treatment of as-prepared Ni NPs with an average particle size of 5.8 nm produced highly metallic Ni NPs covered with thin carbon shells, with negligible particle coarsening. The carbon shells were formed by the segregation of carbons in the Ni lattice to the surface of the Ni NPs, leaving highly metallic Ni NPs. X-ray photoelectron spectroscopic analyses revealed that the atomic ratio of metallic Ni increased from 19.2 to 71.7% as a result of the heat treatment. The NPs exhibited higher electrocatalytic activities toward the hydrazine oxidation reaction in alkaline solution, as compared to those of the as-prepared Ni NPs and commercial Ni powders.
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Nanomaterials for catalytic reactions · Supercapacitor Materials and Fabrication

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

JST CREST, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan

Funding

Ministry of Education, Culture, Sports, Science, and Technology · Core Research for Evolutional Science and Technology, Japan Science and Technology Agency

References (30)

Show source-provided references
1. Wang C. · J. Am. Chem. Soc. · 2011 · 133 · 1439610.1021/ja2047655 ↗
2. Sun S. H. · Science · 2000 · 287 · 198910.1126/science.287.5460.1989 ↗
3. Hyeon T. · Chem. Commun. · 2003 · 92710.1039/b207789b ↗
4. Elkins K. E. · Nano Lett. · 2003 · 3 · 164710.1021/nl034734w ↗
5. Hou Y. L. · Chem. Mater. · 2004 · 16 · 514910.1021/cm048902c ↗
6. Sanabria-Chinchilla J. · J. Am. Chem. Soc. · 2011 · 133 · 542510.1021/ja111160r ↗
7. Reske R. · J. Phys. Chem. Lett. · 2013 · 4 · 241010.1021/jz401087q ↗
8. Sakamoto T. · Catal. Today · 2011 · 164 · 18110.1016/j.cattod.2010.11.012 ↗
9. Sakamoto T. · J. Power Sources · 2014 · 247 · 60510.1016/j.jpowsour.2013.08.107 ↗
10. Yang H. · RSC Adv. · 2012 · 2 · 503810.1039/c2ra01346k ↗
11. Jeon T. Y. · J. Phys. Chem. C · 2009 · 113 · 1973210.1021/jp9076273 ↗
12. Ghosh T. · Chem. Mater. · 2010 · 22 · 219010.1021/cm9018474 ↗
13. Trotochaud L. · J. Am. Chem. Soc. · 2012 · 134 · 1725310.1021/ja307507a ↗
14. Sapieszko R. S. · J. Colloid Interface Sci. · 1980 · 74 · 40510.1016/0021-9797(80)90210-6 ↗
15. Sun S. H. · J. Am. Chem. Soc. · 2002 · 124 · 820410.1021/ja026501x ↗
16. Park J. · Adv. Mater. · 2005 · 17 · 42910.1002/adma.200400611 ↗
17. Railsback J. G. · ACS Nano · 2010 · 4 · 191310.1021/nn901736y ↗
18. Ioannides T. · J. Catal. · 1996 · 161 · 56010.1006/jcat.1996.0218 ↗
19. Ding M. N. · J. Phys. Chem. Lett. · 2013 · 4 · 14710.1021/jz301711a ↗
20. Otsuka K. · Carbon · 2004 · 42 · 72710.1016/j.carbon.2003.12.076 ↗
21. Li X. S. · Nano Lett. · 2009 · 9 · 426810.1021/nl902515k ↗
22. Yoon S. M. · ACS Nano · 2012 · 6 · 680310.1021/nn301546z ↗
23. Krishnankutty N. · Appl. Catal., A · 1998 · 173 · 13710.1016/S0926-860X(98)00173-2 ↗
24. Jeon T. Y. · Langmuir · 2012 · 28 · 366410.1021/la2042668 ↗
25. Ziemecki S. B. · J. Am. Chem. Soc. · 1985 · 107 · 454710.1021/ja00301a031 ↗
26. Bowker M. · J. Phys. Chem. C · 2010 · 114 · 506010.1021/jp9108046 ↗
27. Matienzo L. J. · Inorg. Nucl. Chem. Lett. · 1972 · 8 · 108510.1016/0020-1650(72)80198-3 ↗
28. Matienzo L. J. · Inorg. Chem. · 1973 · 12 · 276210.1021/ic50130a005 ↗
29. Hall D. S. · J. Electrochem. Soc. · 2013 · 160 · F23510.1149/2.026303jes ↗
30. Corrigan D. A. · J. Electrochem. Soc. · 1989 · 136 · 72310.1149/1.2096717 ↗