Monodisperse Octahedral α-MnS and MnO Nanoparticles by the Decomposition of Manganese Oleate in the Presence of Sulfur
Source abstract
Abstract
Octahedral monodisperse α-MnS and MnO nanoparticles have been synthesized by decomposing manganese oleate and elemental sulfur in octadecene at high (250−320 °C) temperature. The chemical composition of the obtained NPs depends on the Mn:S ratio in an unexpected way. Pure α-MnS NP samples are obtained when S:Mn ≥ 2:1, whereas pure MnO NPs require S:Mn ≤ 0.6. Variation of several parameters (concentration of sulfur, heating rate and aging temperature and time) resulted in a α-MnS NP size interval of 11−14 (from Mn monooleate) and 18−30 nm (from Mn dioleate). For MnO NPs only, size control is also possible by addition of free oleic acid (14−24 nm). Analysis of TEM tilting experiments and electron diffraction shows that both α-MnS and MnO nanoparticles have octahedral shape and spontaneously form ordered arrays with strong texture in the {111} direction. Measurement of the magnetic properties showed that α-MnS nanoparticles consist of an antiferromagnetic core and a ferromagnetic-like shell that are exchange coupled below the blocking temperature of the shell (23 K for 29 nm α-MnS NP).
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Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Laboratorio di Nanotecnologie, Istituto di Scienze e Tecnologie Molecolari, Consiglio Nazionale delle Ricerche, via G. Fantoli 16/15, 20138 Milano, Italy
Istituto di Scienze e Tecnologie Molecolari, Consiglio Nazionale delle Ricerche, via C. Golgi 19, 20133 Milano, Italy
Centro Interdipartimentale di Microscopia Avanzata, Università degli Studi di Milano, via G. Celoria 26, 20133 Milano, Italy
References (47)
Show source-provided references
1. Kan S. H. · Isr. J. Chem. · 2001 · 41 · 5510.1560/1FB3-1PF4-72JQ-0AQC ↗
2. Furdyna J. K. · J. Appl. Phys. · 1987 · 61 · 352610.1063/1.338714 ↗
3. Kim D. S. · J. Phys. Chem. B · 2006 · 110 · 1826210.1021/jp063965z ↗
4. Skromme B. J. · Appl. Phys. Lett. · 1995 · 67 · 269010.1063/1.114294 ↗
5. Zhang N. · Mater. Chem. Phys. · 2008 · 111 · 1310.1016/j.matchemphys.2008.03.040 ↗
6. Zhang X. V. · J. Am. Chem. Soc. · 2004 · 126 · 1124710.1021/ja0476415 ↗
7. Michel F. M. · Chem. Mater. · 2006 · 18 · 172610.1021/cm048320v ↗
8. Biswas S. · J. Cryst. Growth · 2005 · 284 · 12910.1016/j.jcrysgro.2005.06.043 ↗
9. Jiang J. H. · Mater. Chem. Phys. · 2009 · 115 · 50210.1016/j.matchemphys.2009.01.012 ↗
10. Ma D. K. · Chem. Phys. Lett. · 2008 · 462 · 9610.1016/j.cplett.2008.07.078 ↗
11. An C. H. · J. Cryst. Growth · 2003 · 252 · 57510.1016/S0022-0248(03)01001-7 ↗
12. Ge J. P. · Chem. Commun. · 2003 · 2498
13. Ge J. P. · Chem. Eur. J. · 2004 · 10 · 352510.1002/chem.200400008 ↗
14. Jun Y. W. · J. Am. Chem. Soc. · 2002 · 124 · 61510.1021/ja016887w ↗
15. Pradhan N. · J. Phys. Chem. B · 2003 · 107 · 1384310.1021/jp035795l ↗
16. Tian L. · Cryst. Growth Des. · 2009 · 9 · 35210.1021/cg800536w ↗
17. Joo J. · J. Am. Chem. Soc. · 2003 · 125 · 1110010.1021/ja0357902 ↗
18. Choi S. H. · Adv. Funct. Mater. · 2009 · 19 · 164510.1002/adfm.200800832 ↗
19. Jana N. R. · Chem. Mater. · 2004 · 16 · 393110.1021/cm049221k ↗
20. Park J. · Nat. Mater. · 2004 · 3 · 89110.1038/nmat1251 ↗
21. Hyeon T. · J. Am. Chem. Soc. · 2001 · 123 · 1279810.1021/ja016812s ↗
22. Na H. B. · Angew. Chem., Int. Ed. · 2007 · 46 · 539710.1002/anie.200604775 ↗
23. Berkowitz A. E. · J. Phys. D: Appl. Phys. · 2008 · 13400710.1088/0022-3727/41/13/134007 ↗
24. Berkowitz A. E. · Phys. Rev. B · 2008 · 77 · 02440310.1103/PhysRevB.77.024403 ↗
25. Pan D. P. J. · Chem. Commun. · 2009 · 323410.1039/b902875g ↗
26. Li Q. · Cryst. Growth Des. · 2009 · 9 · 310010.1021/cg800876p ↗
27. Schladt T. D. · Chem. Mater. · 2009 · 21 · 318310.1021/cm900663t ↗
28. Chen Y. F. · J. Am. Chem. Soc. · 2007 · 129 · 1093710.1021/ja073023n ↗
29. Lee S. Y. · J. Colloid Interface Sci. · 2006 · 293 · 40110.1016/j.jcis.2005.06.062 ↗
30. Seo W. S. · Angew. Chem., Int. Ed. · 2004 · 43 · 111510.1002/anie.200352400 ↗
31. Si H. L. · CrystEngComm · 2009 · 11 · 112810.1039/b901603c ↗
32. Yin M. · J. Am. Chem. Soc. · 2003 · 125 · 1018010.1021/ja0362656 ↗
33. Malik A. S. · J. Mater. Chem. · 2003 · 13 · 212310.1039/b303551d ↗
34. Lutterotti, L.; Matthies, S.; Wenk, H.R.InProceedings of the Twelfth International Conference on Textures of Materials;Montreal, Aug 9−13, 1999;National Research Council of Canada:Ottawa, ON, 1999; Vol.1, p1599.
35. Tian Z. R. · Science · 1997 · 276 · 92610.1126/science.276.5314.926 ↗
36. Williams D. B. · 200910.1007/978-0-387-76501-3 ↗
37. Zitoun D. · J. Am. Chem. Soc. · 2005 · 127 · 1503410.1021/ja0555926 ↗
38. Ould-Ely T. · Chem. Mater. · 2006 · 18 · 182110.1021/cm052492q ↗
39. Rusakova I. · Chem. Mater. · 2007 · 19 · 136910.1021/cm062649u ↗
40. Peng X. G. · Adv. Mater. · 2003 · 15 · 45910.1002/adma.200390107 ↗
41. Rondinone A. J. · J. Phys. Chem. B · 1999 · 103 · 687610.1021/jp9912307 ↗
42. Dormann J. L. · Adv. Chem. Phys. · 1997 · 98 · 283
43. Aharoni A. · 2000
44. Corliss L. · Phys. Rev. · 1956 · 104 · 92410.1103/PhysRev.104.924 ↗
45. Pearce C. I. · Sulfide Mineral. Geochem. · 2006 · 61 · 12710.2138/rmg.2006.61.3 ↗
46. Nogués J. · Phys. Rep. · 2005 · 422 · 6510.1016/j.physrep.2005.08.004 ↗
47. Fiorani D. · 200510.1007/b136494 ↗