Effect of Ligand−Metal Interactions on the Growth of Transition-Metal and Alloy Nanoparticles
Source abstract
Abstract
The growth of cobalt, iron, and platinum and their alloy nanoparticles was investigated with oleic acid and trioctylphosphine oxide as ligands. Both the ligand type and concentration are important in determining the final product of the reactions. With a high concentration of oleic acid, thermal decomposition of dicobalt octacarbonyl and iron pentacarbonyl precursors yields only molecular cluster complex species with oxidized metal centers. However, reduction of platinum acetylacetonate under identical conditions yields nanometer-sized particles. In the presence of a high concentration of trioctylphosphine oxide, only the cobalt system was observed to form a cluster−complex species, while both the iron and platinum systems form nanometer-sized particles. This oxidation process, which forms cluster complexes, provides a digestive ripening mechanism that competes with the Ostwald ripening process, thus affecting the particle size and composition of both the pure metal and alloy nanoparticles.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Iron oxide chemistry and applications · Electrocatalysts for Energy Conversion · Catalytic Processes in Materials Science
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Chemistry Division, Materials Science Division, and Center for Nanoscale Materials, Argonne National Laboratory, Argonne, Illinois 60439 and Department of Chemistry, University of Chicago, 5635 South Ellis Avenue, Chicago, Illinois 60637
References (33)
Show source-provided references
1. Murray C. B. · MRS Bull. · 2001 · 26 · 99110.1557/mrs2001.254 ↗
2. Narayanan R. · J. Phys. Chem. B · 2005 · 109 · 12676
3. Li G. X. · IEEE Trans. Magn. · 2004 · 40 · 3002
4. Ito A. · J. Biosci. Bioeng. · 2005 · 100 · 11
5. Weller D. · IEEE Trans. Magn. · 1999 · 35 · 443910.1109/20.809134 ↗
6. Zeng H. · Nature · 2002 · 420 · 39810.1038/nature01208 ↗
7. Hyeon T. · Chem. Commun. · 2003 · 8 · 934
8. Puntes V. F. · Science · 2001 · 291 · 211710.1126/science.1058495 ↗
9. Park S.-J. · J. Am. Chem. Soc. · 2000 · 122 · 8582
10. Park J. · J. Am. Chem. Soc. · 2004 · 126 · 9078
11. Shevchenko E. V. · J. Am. Chem. Soc. · 2002 · 124 · 11485
12. Sun S. · Science · 2000 · 287 · 199210.1126/science.287.5460.1992 ↗
13. Chen M. · J. Am. Chem. Soc. · 2004 · 126 · 8395
14. Chen M. · Nano Lett. · 2002 · 2 · 214
15. Massalski T. · 1990 · 2
16. Klemmer T. J. · Appl. Phys. Lett. · 2002 · 81 · 222210.1063/1.1507837 ↗
17. Stahl B. · Phys. Rev. B · 2003 · 67 · 01443410.1103/PhysRevB.67.014422 ↗
18. Ulmeanu M. · Phys. Rev. B · 2004 · 69 · 05442310.1103/PhysRevB.69.054417 ↗
19. Sun S. · IEEE. Trans. Magn. · 2001 · 37 · 1243
20. Samia A. C. S. · J. Am. Chem. Soc. · 2005 · 127 · 4127
21. Cullity B. D. · 1972
22. Suslick K. S. · J. Am Chem. Soc. · 1996 · 118 · 1196110.1021/ja961807n ↗
23. Wu N. · Nano Lett. · 2004 · 4 · 386
24. Nakamoto K. · 1997
25. Stahl B. · Adv. Mater. · 2002 · 14 · 2710.1002/1521-4095(20020104)14:1<24::AID-ADMA24>3.0.CO;2-O ↗
26. Howard L. E. M. · J. Am. Chem. Soc. · 2005 · 127 · 1014010.1021/ja051669e ↗
27. Lin X. M. · J. Nanoparticle Res. · 2000 · 2 · 164
28. Prasad B. L. V. · J. Chem. Mater. · 2003 · 15 · 942
29. Jin R. C. · J. Am. Chem. Soc. · 2004 · 126 · 9901
30. Jana N. R. · Chem. Mater. · 2004 · 16 · 3935
31. Park J. · Nat. Mater. · 2004 · 3 · 89510.1038/nmat1251 ↗
32. Zhou S. · Angew. Chem., Int. Ed. · 2005 · 44 · 454310.1002/anie.200500786 ↗
33. Zinke−Allmang M. · Phys. Rev. Lett. · 1992 · 68 · 2361