journal article·2007-05-01

Dendritic Silver Nanostructure Growth and Evolution in Replacement Reaction

Jixiang Fang, Hongjun You, Peng Kong, Yan Yi, Xiaoping Song, Bingjun Ding

Crystal Growth & Design· Volume 7· Issue 5
Publisher page

Abstract

In this study, a well-defined dendritic silver nanostructure can be large-scale synthesized in AgNO 3 (aqueous) at room temperature. The nonequilibrium and anisotropic growth at different silver ion concentrations result in controllable morphologies and morphological evolution. At high silver ion concentrations, a strong anisotropic growth contributes to a fine single crystalline silver dendrite. As the reaction proceeds, the dendritic structure transforms into a thermodynamically stable hexagonal structure. At a relatively low silver ion concentration, a particle-aggregated fractal pattern can be obtained due to relatively small anisotropy. As the reaction time increases, the transition from polycrystalline aggregates to a single crystal during silver dendritic growth can be observed. An oriented attachment mechanism can be used to explain the structural and morphological evolution of silver nanostructures. Silver nanostructures with various morphologies are expected to have significant potential applications in superhydrophobic surfaces, surface-enhanced Raman scattering, and others.
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Research context

OpenAlex topics: Nanocluster Synthesis and Applications · Gold and Silver Nanoparticles Synthesis and Applications · Nanomaterials and Printing Technologies

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

Affiliations

School of Science, State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University, Shann Xi, 710049, People's Republic of China

References (25)

Show source-provided references
1. Yugang S. · Science · 2002 · 298 · 2176
2. Rongchao J. · Nature · 2003 · 425 · 487
3. Aizawa M. · Nano Lett. · 2005 · 5 · 81510.1021/nl048008k ↗
4. Peng X. G. · Nature · 2000 · 404 · 5910.1038/35003535 ↗
5. Dick K. A. · Nat. Mater. · 2004 · 3 · 38010.1038/nmat1133 ↗
6. Dick K. A. · Nat. Mater. · 2004 · 3 · 38010.1038/nmat1133 ↗
7. Xiaqin W. · Chem. Commun. · 2002 · 1300
8. Imai H. · Cryst. Growth Des. · 2005 · 5 · 107310.1021/cg0496585 ↗
9. Jianping X. · Adv. Mater. · 2001 · 13 · 188710.1002/1521-4095(200112)13:24<1887::AID-ADMA1887>3.0.CO;2-2 ↗
10. Zhou Y. · Adv. Mater. · 1999 · 10 · 85010.1002/(SICI)1521-4095(199907)11:10<850::AID-ADMA850>3.0.CO;2-Z ↗
11. Fleury V. · Nature · 2002 · 416 · 71610.1038/416716a ↗
12. Shizhong W. · J. Phys. Chem. B · 2000 · 104 · 568110.1021/jp000225w ↗
13. Socol Y. · Langmuir · 2002 · 18 · 473610.1021/la015689f ↗
14. Wang X. · Langmuir · 2003 · 19 · 624210.1021/la027070z ↗
15. Haohao L. · J. Phys. Chem. B · 2004 · 108 · 1165410.1021/jp049008b ↗
16. Yugang S. · J. Am. Chem. Soc. · 2004 · 126 · 3893
17. Fang J. · Nanotechnology · 2006 · 17 · 584110.1088/0957-4484/17/23/021 ↗
18. Germin V. · J. Phys. Chem. B · 2004 · 107 · 871710.1021/jp0303826 ↗
19. Penn R. L. · Science · 1998 · 281 · 96910.1126/science.281.5379.969 ↗
20. Alivisatos A. P. · Science · 2000 · 289 · 73610.1126/science.289.5480.736 ↗
21. Banfield J. F. · Science · 2000 · 289 · 75110.1126/science.289.5480.751 ↗
22. Fleury V. · Nature · 1997 · 390 · 14510.1038/36522 ↗
23. Wang M. · Phys. Rev. Lett. · 1993 · 71 · 400310.1103/PhysRevLett.71.4003 ↗
24. Washio I. · Adv. Mater. · 2006 · 18 · 174510.1002/adma.200600675 ↗
25. Ming W. · Nano Lett. · 2005 · 5 · 229810.1021/nl0517363 ↗