journal article·2015-10Open access

Oxygen‐Ions‐Mediated Pseudocapacitive Charge Storage in Molybdenum Trioxide Nanobelts

Vipin Kumar, Xu Wang, Pooi See Lee

ChemNanoMat· Volume 1· Issue 6

Abstract

Abstract Here we demonstrate the effect of the concentration of hydrogen peroxide solution on the generation of various kinds of oxygen ions, mainly peroxide (O22−) and superoxide (O2−) ions, on the surface of molybdenum trioxide (MoO3) nanobelts. Due to O22− and O2− ions, the mechanism of charge storage shows an interplay between surface‐controlled and diffusion‐controlled redox reactions. The concentration of H2O2 is indicative of the strength of hydrogen bonding, which significantly affects the concentration or coordination of the surface species (O2−, O22−, Mo5+ and Mo6+) that are available to interact with the electrolyte ions. By altering the concentration of the surface species (IO2−/IO22−, IMo5+/IMo6+), a specific capacitance as high as 210 F g−1 is achieved for MoO3 nanobelts at an applied current density of 0.5 A g−1, with relatively good cycling stability (≈85 %) after 2000 cycles.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Supercapacitor Materials and Fabrication · Advancements in Battery Materials · Transition Metal Oxide Nanomaterials

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

Affiliations

School of Materials Science and Engineering Nanyang Technological University Singapore 639798 Singapore

Funding

NTU Singapore · Temasek Laboratories@NTU

References (32)

Show source-provided references
1. 10.1021/ja00325a01110.1021/ja00325a011 ↗
2. Kung H. H. · 1991
3. 10.1039/c3986000071410.1039/c39860000714 ↗
4. 10.1149/1.326547610.1149/1.3265476 ↗
5. 10.1016/S1452-3981(23)08076-810.1016/S1452-3981(23)08076-8 ↗
6. 10.1016/j.electacta.2012.03.15110.1016/j.electacta.2012.03.151 ↗
7. 10.1039/C1CS15060J10.1039/C1CS15060J ↗
8. 10.1039/c1cc13474d10.1039/c1cc13474d ↗
9. 10.1021/la027020u10.1021/la027020u ↗
10. 10.1016/j.matlet.2013.03.00510.1016/j.matlet.2013.03.005 ↗
11. 10.1021/cm502558t10.1021/cm502558t ↗
12. 10.1149/1.138899510.1149/1.1388995 ↗
13. 10.1038/nmat261210.1038/nmat2612 ↗
14. 10.1039/c2ta01120d10.1039/c2ta01120d ↗
15. 10.1021/jp108778v10.1021/jp108778v ↗
16. 10.1002/adfm20130185110.1002/adfm201301851 ↗
17. Li S. · Int. J. Electrochem. Sci. · 2011 · 6 · 450410.1016/S1452-3981(23)18345-3 ↗
18. 10.1016/j.electacta.2012.11.06710.1016/j.electacta.2012.11.067 ↗
19. 10.1038/ncomms370110.1038/ncomms3701 ↗
20. 10.1021/am500855a10.1021/am500855a ↗
21. 10.1039/c3ce41341a10.1039/c3ce41341a ↗
22. 10.1016/0022-4596(91)90064-O10.1016/0022-4596(91)90064-O ↗
23. 10.1021/cg201500b10.1021/cg201500b ↗
24. 10.1039/c1cc14030b10.1039/c1cc14030b ↗
25. 10.1016/j.electacta.2010.09.02810.1016/j.electacta.2010.09.028 ↗
26. 10.1016/0039-6028(92)90042-510.1016/0039-6028(92)90042-5 ↗
27. 10.1006/jcat.1993.112410.1006/jcat.1993.1124 ↗
28. 10.1006/jcat.1993.101710.1006/jcat.1993.1017 ↗
29. 10.1007/BF0104538510.1007/BF01045385 ↗
30. 10.1002/adma.20120334610.1002/adma.201203346 ↗
31. 10.1002/adma.20130609710.1002/adma.201306097 ↗
32. 10.1038/nmat360110.1038/nmat3601 ↗