journal article·2004-06-01

Preparation and Thermal Stability of Gold Nanoparticles in Silk-Templated Porous Filaments of Titania and Zirconia

Junhui He, Toyoki Kunitake

Chemistry of Materials· Volume 16· Issue 13
Publisher page

Abstract

Porous metal-oxide filaments were readily fabricated using hydrophobic silk as template via the surface sol−gel process, followed by removal of the organic components. Such biotemplated porous matrixes were employed as nanoreactors for in situ synthesis of gold nanoparticles by NaBH 4 reduction of the incorporated gold ion. The as-synthesized nanoparticle (ca. 4 nm) was apparently stabilized by the porous morphology of the silk-templated matrix, as well as by the coordinative interaction between the surface Au atom of the nanoparticle with the surrounding oxygen linkage of the matrix. The nanoparticle showed only a small increase (to ca. 6 nm) in particle size after annealing at 500 °C for 5 h, but it became much larger (∼40 nm) at 800 °C. Under the otherwise identical conditions, amorphous zirconia matrix gave rise to a much smaller size increase (ca. 10 nm at 800 °C), indicating more effective suppression of fusion of molten gold nanoparticles. Apparently, better physical isolation of the nanoparticle was attained for amorphous zirconia than nanocrystalline titania. General features of the formation of metal nanoparticles in solid matrixes were discussed, in terms of morphology and functionality of matrixes.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoporous metals and alloys · Pickering emulsions and particle stabilization · Gold and Silver Nanoparticles Synthesis and Applications

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

Affiliations

Frontier Research System, The Institute of Physical and Chemical Research (RIKEN), Hirosawa 2-1, Wako, Saitama 351-0198, Japan

References (29)

Show source-provided references
1. Wark M. · Phys. Chem. Chem. Phys. · 2003 · 5 · 519410.1039/B308139G ↗
2. Govindaraj R. · J. Appl. Phys. · 2001 · 90 · 96310.1063/1.1382831 ↗
3. Haus J. W. · J. Opt. Soc. Am. B · 1989 · 6 · 807
4. Tanaka A. · Phys. Rev. B · 1993 · 47 · 124310.1103/PhysRevE.47.1243 ↗
5. Solinas S. · J. Acta Mater. · 2001 · 49 · 281110.1016/S1359-6454(01)00160-4 ↗
6. Bell A. T. · Science · 2003 · 299 · 169110.1126/science.1083622 ↗
7. Rolison D. R. · Science · 2003 · 299 · 170110.1126/science.1082332 ↗
8. Vendange V. · J. Sol-Gel Sci., Technol. · 1998 · 11 · 30710.1023/A:1008614514565 ↗
9. Davis S. A. · Nature · 1997 · 385 · 42310.1038/385420a0 ↗
10. Dong A. · Adv. Mater. · 2002 · 14 · 929
11. Mayes E. L. · Adv. Mater. · 1998 · 10 · 80510.1002/(SICI)1521-4095(199807)10:10<801::AID-ADMA801>3.0.CO;2-I ↗
12. Huang L. · J. Mater. Chem. · 2003 · 13 · 668
13. Salamone J. C. · 7719
14. Borovskii V. R. · Teplofiz. Teplotekh. · 1973 · 25 · 52
15. Ichinose I. · Chem. Lett. · 1996 · 831 · 832
16. He J. · Chem. Mater. · 2002 · 14 · 3500
17. He J. · Langmuir · 2002 · 18 · 10010
18. He J. · Chem. Commun. · 2002 · 1910 · 1911
19. He J. · J. Am. Chem. Soc. · 2003 · 125 · 11040
20. Fujikawa S. · Langmuir · 2003 · 19 · 655210.1021/la026979e ↗
21. Huang J. · J. Am. Chem. Soc. · 2003 · 125 · 1183410.1021/ja037419k ↗
22. He J. · Chem. Mater. · 2003 · 15 · 4406
23. Franke R. · J. Am. Chem. Soc. · 1996 · 118 · 1209710.1021/ja953525d ↗
24. Buffat · Phys. Rev. A · 1976 · 13 · 229710.1103/PhysRevA.13.2287 ↗
25. Möckel H. · J. Mater. Chem. · 1999 · 9 · 305610.1039/a905373e ↗
26. Lide, D. R.; Ed,CRC Handbook of Chemistry and Physics, 81st ed.; CRC Press LLC: Boca Raton, FL, 2000; pp 4−100.
27. Lele A. K. · Chem. Eng. Sci. · 2001 · 56 · 5800
28. Fullam S. · Adv. Mater. · 2000 · 12 · 143210.1002/1521-4095(200010)12:19<1430::AID-ADMA1430>3.0.CO;2-8 ↗
29. Baumann T. F. · Chem. Mater. · 2003 · 15 · 374710.1021/cm0343960 ↗