Does Morphology of a Metal Nanoparticle Play a Role in Ostwald Ripening Processes?
Source abstract
Abstract
The Ostwald ripening theory is commonly adopted to rationalize the growth of large metal nanoparticles that are formed at the expense of small-sized nanoparticles of higher chemical potential energies. This classical theory did not describe whether the morphology of a metal nanoparticle plays a role in controlling the shape evolution in the ripening processes. Here we show the direct observation of shape evolution among Ag nanoparticles of different morphologies in solutions, and experimental measurements of the relative chemical potential energies (or the electrochemical oxidation potentials) of Ag NPs of different morphologies, including, nanocubes, nanospheres, triangular plates, and decahedral nanoparticles. Theoretical calculation shows that when the diameter of a metal NP is beyond 35 nm, the influence of particle sizes on the oxidation potentials becomes very small. Chemical etching of Ag NPs by Fe(NO 3 ) 3 results in preferential removal of atoms at sharp edges/corners, and negative shift in the oxidation potentials. The measured electrochemical oxidation potentials of Ag NPs are in following orders: nanocubes (43 nm in length, 346 mV Ag/AgCl ) > nanospheres (53 nm in diameter, 337 mV Ag/AgCl ) > penta-twinned decahedrons (86 nm in edge length, 315 mV Ag/AgCl ) > triangular nanoplates (127 nm in edge length and 11 nm in thickness, 293 mV Ag/AgCl ).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Copper-based nanomaterials and applications · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan
References (50)
Show source-provided references
1. Wiley B. J. · Nano Lett. · 2007 · 7 · 103210.1021/nl070214f ↗
2. Zhang Q. A. · J. Am. Chem. Soc. · 2010 · 132 · 1137210.1021/ja104931h ↗
3. Sun Y. G. · Science · 2002 · 298 · 217610.1126/science.1077229 ↗
4. Tsuji M. · Cryst. Growth Des. · 2009 · 9 · 470010.1021/cg900563y ↗
5. Kan C. X. · J. Phys. D–Appl. Phys · 2008 · 41 · 15530410.1088/0022-3727/41/15/155304 ↗
6. Pietrobon B. · Chem. Mater. · 2008 · 20 · 518610.1021/cm800926u ↗
7. Zhang J. A. · J. Am. Chem. Soc. · 2010 · 132 · 1250210.1021/ja106008b ↗
8. Stamplecoskie K. G. · J. Am. Chem. Soc. · 2010 · 132 · 182510.1021/ja910010b ↗
9. Zhang Q. · Angew. Chem., Int. Ed. · 2009 · 48 · 351610.1002/anie.200900545 ↗
10. Redmond P. L. · Nano Lett. · 2005 · 5 · 13110.1021/nl048204r ↗
11. Madras G. · J. Chem. Phys. · 2002 · 117 · 804210.1063/1.1510769 ↗
12. Baldan A. · J. Mater. Sci. · 2002 · 37 · 217110.1023/A:1015388912729 ↗
13. Ostwald W. · 1896 · 2
14. Liz-Marzan L. M. · Langmuir · 2006 · 22 · 3210.1021/la0513353 ↗
15. Smith A. M. · Nat. Nanotechnol. · 2009 · 4 · 5610.1038/nnano.2008.360 ↗
16. Tao A. · Angew. Chem., Int. Ed. · 2006 · 45 · 459710.1002/anie.200601277 ↗
17. Mock J. J. · J. Chem. Phys. · 2002 · 116 · 675510.1063/1.1462610 ↗
18. Haes A. J. · J. Am. Chem. Soc. · 2002 · 124 · 1059610.1021/ja020393x ↗
19. McLellan J. M. · Nano Lett. · 2007 · 7 · 101310.1021/nl070157q ↗
20. Chen D. P. · J. Mater. Sci. · 2009 · 44 · 107610.1007/s10853-008-3204-y ↗
21. Vaddiraju S. · Adv. Funct. Mater. · 2008 · 18 · 192910.1002/adfm.200800196 ↗
22. Tian N. · Science · 2007 · 316 · 73210.1126/science.1140484 ↗
23. Lee I. · Nat. Mater. · 2009 · 8 · 13210.1038/nmat2371 ↗
24. Xu R. · Chem. Asian. J. · 2006 · 1 · 88810.1002/asia.200600260 ↗
25. Zumdahl, S. S.Chemical Principle;Houghton Mifflin Company:New York, 2005; Vol.5, pp471–473.
26. Ivanova O. S. · J. Am. Chem. Soc. · 2010 · 132 · 7010.1021/ja908780g ↗
27. Chaki N. K. · Phys. Chem. Chem. Phys. · 2004 · 6 · 130410.1039/B312643A ↗
28. Henglein A. · J. Phys. Chem. · 1993 · 97 · 545710.1021/j100123a004 ↗
29. Plieth W. J. · J. Phys. Chem. · 1982 · 86 · 316610.1021/j100213a020 ↗
30. Ming T. · J. Am. Chem. Soc. · 2009 · 131 · 1635010.1021/ja907549n ↗
31. Zhang J. A. · J. Am. Chem. Soc. · 2010 · 132 · 1401210.1021/ja106394k ↗
32. Aherne D. · Adv. Funct. Mater. · 2008 · 18 · 200510.1002/adfm.200800233 ↗
33. Siekkinen A. R. · Chem. Phys. Lett. · 2006 · 432 · 49110.1016/j.cplett.2006.10.095 ↗
34. Skrabalak S. E. · Nat. Protoc. · 2007 · 2 · 218210.1038/nprot.2007.326 ↗
35. Xia Y. N. · Angew. Chem., Int. Ed. · 2009 · 48 · 6010.1002/anie.200802248 ↗
36. Tang Y. · Nat. Mater. · 2007 · 6 · 75410.1038/nmat1982 ↗
37. Johnson C. L. · Nat. Mater. · 2008 · 7 · 12010.1038/nmat2083 ↗
38. Niu W. X. · Nano Today · 2011 · 6 · 26510.1016/j.nantod.2011.04.006 ↗
39. Pastoriza-Santos I. · J. Mater. Chem. · 2008 · 18 · 172410.1039/b716538b ↗
40. Wiley B. · Chem.—Eur. J. · 2005 · 11 · 45410.1002/chem.200400927 ↗
41. Xiong Y. J. · Angew. Chem., Int. Ed. · 2007 · 46 · 715710.1002/anie.200702473 ↗
42. Liu C. H. · Sensors · 2007 · 7 · 70810.3390/s7050708 ↗
43. McEachran M. · Chem. Commun. · 2008 · 44 · 573710.1039/b813519c ↗
44. Germain V. · J. Phys. Chem. B · 2003 · 107 · 871710.1021/jp0303826 ↗
45. Rocha T. C. R. · J. Phys. Chem. C · 2007 · 111 · 698910.1021/jp0702696 ↗
46. Wang Z. L. · J. Phys. Chem. B · 2000 · 104 · 115310.1021/jp993593c ↗
47. Niu W. X. · J. Am. Chem. Soc. · 2009 · 131 · 69710.1021/ja804115r ↗
48. Johnson C. J. · J. Mater. Chem. · 2002 · 12 · 176510.1039/b200953f ↗
49. Sun Y. · Nano Lett. · 2003 · 3 · 95510.1021/nl034312m ↗
50. Kuo C. L. · Langmuir · 2012 · 28 · 372210.1021/la204002b ↗