journal article·2001-11-01

Manganese Vanadium Oxide Nanotubes: Synthesis, Characterization, and Electrochemistry

Arthur Dobley, Katana Ngala, Shoufeng Yang, Peter Y. Zavalij, M. Stanley Whittingham

Chemistry of Materials· Volume 13· Issue 11
Publisher page

Abstract

Vanadium oxide nanotubes have been formed from the layered vanadium oxide precursor V 2 O 5+ δ [C 12 H 25 NH 3 ]. Both the precursor and tubes have been characterized. The black nanotubes have a relatively low thermal stability in oxygen, being oxidized to V 2 O 5 below 200 °C. A new manganese vanadium oxide nanotube, Mn 0.1 VO 2.5+ δ · n H 2 O, has been synthesized by ion exchange. These manganese tubes have a tetragonal layer with a = 6.157 (3) Å and an interlayer spacing c = 10.52 (3) Å. The nanotubes react with lithium chemically and are also electrochemically active in lithium cells. Two lithium atoms per vanadium can be incorporated chemically from n -butyllithium into both the manganese and the alkylammonium nanotubes. The manganese compound electrochemically intercalates 0.5 lithium per vanadium to a 2 V cutoff, giving a capacity of 140 A h/kg.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Transition Metal Oxide Nanomaterials · Mesoporous Materials and Catalysis · Catalysis and Oxidation Reactions

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

Affiliations

Chemistry Department and the Institute for Materials Research, State University of New York at Binghamton, Binghamton, New York 13902-6016

References (31)

Show source-provided references
1. Kresge C. T. · Nature · 1992 · 359 · 71010.1038/359710a0 ↗
2. Beck J. S. · J. Am. Chem. Soc. · 1992 · 114 · 1083410.1021/ja00053a020 ↗
3. Millet P. · J. Solid State Chem. · 1999 · 147 · 67610.1006/jssc.1999.8473 ↗
4. Chirayil T. A. · Chem. Mater. · 1998 · 10 · 262910.1021/cm980242m ↗
5. Janauer G. G. · Chem. Mater. · 1996 · 8 · 209610.1021/cm960111q ↗
6. Janauer G. G. · Chem. Mater. · 1997 · 9 · 64710.1021/cm9606235 ↗
7. Spahr M. E. · Angew. Chem., Int. Ed. Engl. · 1998 · 37 · 126310.1002/(SICI)1521-3773(19980518)37:9<1263::AID-ANIE1263>3.0.CO;2-R ↗
8. Niederberger M. · Chem. Mater. · 2000 · 12 · 199510.1021/cm001028c ↗
9. Spahr M. E. · J. Electrochem. Soc. · 1999 · 146 · 278010.1149/1.1392008 ↗
10. Reinoso J. M. · Helv. Chim. Acta · 2000 · 83 · 172410.1002/1522-2675(20000809)83:8<1724::AID-HLCA1724>3.0.CO;2-G ↗
11. Zhang F. · Electrochem. Commun. · 2000 · 2 · 6910.1016/S1388-2481(99)00143-5 ↗
12. Whittingham M. S. · J. Electrochem. Soc. · 1976 · 123 · 31510.1149/1.2132817 ↗
13. Leroux F. · Solid State Ionics · 1995 · 80 · 30710.1016/0167-2738(95)00152-V ↗
14. Armstrong A. R. · Nature · 1996 · 381 · 49910.1038/381499a0 ↗
15. Delmas C. · 1996
16. Chirayil T. · J. Electrochem. Soc. · 1996 · 143 · L19310.1149/1.1837083 ↗
17. Chen R. · J. Electrochem. Soc. · 1997 · 144 · L6410.1149/1.1837554 ↗
18. Zhang F. · Electrochem. Commun. · 1999 · 1 · 56410.1016/S1388-2481(99)00113-7 ↗
19. Zhang F. · Electrochem. Commun. · 2000 · 2 · 44510.1016/S1388-2481(00)00058-8 ↗
20. Whittingham M. S. · Solid State Ionics · 2000 · 131 · 10910.1016/S0167-2738(00)00626-3 ↗
21. Zavalij P. Y. · Acta Crystallogr. · 1999 · 55 · 62710.1107/S0108768199004000 ↗
22. Whittingham M. S. · Solid State Ionics · 2000 · 131 · 10910.1016/S0167-2738(00)00626-3 ↗
23. Chirayil T. A. · Chem. Commun. · 1997 · 3310.1039/a606772g ↗
24. Chirayil T. · J. Mater. Chem. · 1997 · 7 · 219310.1039/a704624c ↗
25. Chen R. · J. Mater. Chem. · 1999 · 9 · 9310.1039/a805312j ↗
26. Zhang F. · J. Mater. Chem. · 1999 · 9 · 313710.1039/a907465a ↗
27. Dines M. B. · Mater. Res. Bull. · 1975 · 10 · 28710.1016/0025-5408(75)90115-4 ↗
28. Whittingham M. S. · J. Electrochem. Soc. · 1977 · 124 · 138710.1149/1.2133659 ↗
29. Conley R. T. · 1966
30. Wang X. · J. Chem. Commun. · 1998 · 100910.1039/a802059k ↗
31. Torardi C. C. · Electrochem. Soc. Abstr. · 2000 · 2000 · 79