Synthesis and Magnetic Properties of New [Fe18S25](TETAH)14(TETAH = Protonated Triethylenetetramine) Nanoribbons: An Efficient Precursor to Fe7S8Nanowires and Porous Fe2O3Nanorods
Source abstract
Abstract
A solvothermal reaction in a mixed solvent made of triethylenetetriamine (TETA) and deionized water (DIW) results in the formation of well-defined [Fe 18 S 25 ](TETAH) 14 nanoribbons. A suitable volume ratio of TETA and DIW is essential for the formation of elegant [Fe 18 S 25 ](TETAH) 14 nanoribbons. The [Fe 18 S 25 ](TETAH) 14 nanoribbons can act as efficient precursors for production of either Fe 7 S 8 nanowires or porous α-Fe 2 O 3 nanorods by thermal decomposition of [Fe 18 S 25 ](TETAH) 14 in an argon or air atmosphere. The present study demonstrates that the combination of small molecule polyamine with magnetic semiconductor makes it possible to obtain new hybrid nanostructured materials. The thermal decomposition of this new hybrid material is a powerful tool as a unique pathway for controlled synthesis of transition metal chacolgenide nanomaterials and porous transition metal oxides.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Layered Double Hydroxides Synthesis and Applications · Catalytic Processes in Materials Science · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Division of Nanomaterials & Chemistry, Hefei National Laboratory for Physical Sciences at Microscale, the School of Chemistry and Materials, University of Science and Technology of China, Hefei, 230026, P.R. China
References (34)
Show source-provided references
1. aMitzi, D. B.InProgress in Inorganic Chemistry;Karlin, K. D., Ed.Wiley:New York, 1999; p1.
2. bIshihara, T.InOptical Properties of Low-Dimensional Materials;Ogawa, T., Kanemitsu, Y., Eds.;World Scientific:Singapore, 1995; p289.
3. Huang X. Y. · J. Am. Chem. Soc. · 2000 · 122 · 878910.1021/ja002224n ↗
4. Heulings H. R. · Nano Lett. · 2001 · 1 · 52110.1021/nl015556e ↗
5. Huang X. Y. · Chem. Mater. · 2001 · 13 · 375410.1021/cm010403d ↗
6. Huang X. Y. · J. Am. Chem. Soc. · 2003 · 125 · 704910.1021/ja0343611 ↗
7. Yu S. H. · Adv. Mater. · 2002 · 14 · 29610.1002/1521-4095(20020219)14:4<296::AID-ADMA296>3.0.CO;2-6 ↗
8. Deng Z. X. · Inorg. Chem. · 2002 · 41 · 86910.1021/ic0103502 ↗
9. Deng Z. X. · Inorg. Chem. · 2003 · 42 · 233110.1021/ic025846d ↗
10. Yao W. T. · Small · 2005 · 1 · 32010.1002/smll.200400079 ↗
11. Yao W. T. · Adv. Mater. · 2005 · 17 · 279910.1002/adma.200501343 ↗
12. Nath M. · Chem. Commun. · 2004 · 269810.1039/b412056f ↗
13. Schmid G. · 2004
14. Klabunde K. J. · 200110.1002/0471220620 ↗
15. Fendler J. H. · 199810.1002/9783527612079 ↗
16. Fertman V. E. · 1990
17. Berkovsky B. M. · 1993
18. Hyeon T. · Chem. Commun. · 2003 · 92710.1039/b207789b ↗
19. Zhang J. Z. · 200310.1007/b105377 ↗
20. Ennaoui A. · Sol. Cells · 1984 · 13 · 19710.1016/0379-6787(84)90009-7 ↗
21. Ennaoui A. · J. Electrochem. Soc. · 1985 · 132 · 157910.1149/1.2114168 ↗
22. Ennaoui A. · J. Electrochem. Soc. · 1986 · 133 · 9710.1149/1.2108553 ↗
23. Qian X. F. · Mater. Lett. · 2001 · 48 · 10910.1016/S0167-577X(00)00288-3 ↗
24. Nath M. · Adv. Mater. · 2003 · 15 · 209810.1002/adma.200306042 ↗
25. Vaughan D. J. · Sci. Prog. · 1991 · 75 · 371
26. Qian X. F. · Mater. Sci. Eng., B · 1999 · 64 · 17010.1016/S0921-5107(99)00145-2 ↗
27. Chen X. Y. · Chem. Phys. Lett. · 2005 · 403 · 39610.1016/j.cplett.2005.01.050 ↗
28. Kar S. · Chem. Phys. Lett. · 2004 · 398 · 2210.1016/j.cplett.2004.09.028 ↗
29. Kar S. · Mater. Lett. · 2005 · 59 · 28910.1016/j.matlet.2004.10.005 ↗
30. Yu S. H. · J. Mater. Chem. · 1999 · 9 · 128310.1039/a809779h ↗
31. Gao P. · Cryst. Growth Des. · 2006 · 6 · 58310.1021/cg0503548 ↗
32. He Z. B. · Adv. Funct. Mater. · 2006 · 16 · 110510.1002/adfm.200500580 ↗
33. Dong C · J. Appl. Crystallogr. · 1999 · 32 · 83810.1107/S0021889899003039 ↗
34. Zhong L. S. · Adv. Mater. · 2006 · 18 · 242610.1002/adma.200600504 ↗