Green Synthesis of Au Nanostructures at Room Temperature Using Biodegradable Plant Surfactants
Source abstract
Abstract
One-step green synthesis of gold (Au) nanostructures is described using naturally occurring biodegradable plant surfactants such as VeruSOL-3 (mixture of d -limonene and plant-based surfactants), VeruSOL-10, VeruSOL-11, and VeruSOL-12 (individual plant-based surfactants derived from coconut and castor oils) without any special reducing agent/capping agents. This greener method uses water as a benign solvent and surfactant/plant extract as a reducing agent. Depending upon the Au concentration used for the preparation, Au crystallizes in different shapes and sizes to form spherical, prisms, and hexagonal structures. Sizes vary from the nanometer to micrometer scale level depending on the plant extract used for preparation. Synthesized Au nanostructures were characterized using scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and UV spectroscopy.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Nanoparticles: synthesis and applications · Copper-based nanomaterials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Sustainable Technology Division, US Environmental Protection Agency, National Risk Management Research Laboratory, 26 West Martin Luther King Drive, MS 443, Cincinnati, Ohio 45268
VeruTEK Technologies, Inc., 65 West Dudley Town Road, Suite 100, Bloomfield, Connecticut 06002
References (34)
Show source-provided references
1. Millstone J. E. · J. Am. Chem. Soc. · 2005 · 127 · 531210.1021/ja043245a ↗
2. Lee J. −S. · Anal. Chem. · 2008 · 80 · 680510.1021/ac801046a ↗
3. Rosi N. L. · Chem. Rev. · 2005 · 105 · 154710.1021/cr030067f ↗
4. Sau T. K. · J. Am. Chem. Soc. · 2004 · 126 · 864810.1021/ja047846d ↗
5. Gole A. · Chem. Mater. · 2004 · 16 · 363310.1021/cm0492336 ↗
6. Gou L. · Chem. Mater. · 2005 · 17 · 366810.1021/cm050525w ↗
7. Gole A. · Langmuir · 2005 · 21 · 1075610.1021/la0512704 ↗
8. Sau T. K. · Langmuir · 2004 · 20 · 641410.1021/la049463z ↗
9. El-Sayed M. A. · Acc. Chem. Res. · 2001 · 34 · 25710.1021/ar960016n ↗
10. Kundu S. · Langmuir · 2008 · 24 · 966810.1021/la801633r ↗
11. Shankar S. S. · Chem. Mater. · 2005 · 17 · 56610.1021/cm048292g ↗
12. Joshi H. M. · Langmuir · 2006 · 22 · 30010.1021/la051982u ↗
13. Ahmad A. · Langmuir · 2003 · 19 · 355010.1021/la026772l ↗
14. Shukla S. · Chem. Mater. · 2005 · 17 · 500010.1021/cm051165f ↗
15. Lu X. · J. Am. Chem. Soc. · 2008 · 130 · 890010.1021/ja803343m ↗
16. Chen J. · Langmuir · 2007 · 23 · 412010.1021/la063193y ↗
17. Lim B. · Langmuir · 2008 · 24 · 1043710.1021/la801803z ↗
18. Thomas K. G. · J. Am. Chem. Soc. · 2000 · 122 · 265510.1021/ja9941835 ↗
19. Raveendran P. · J. Am. Chem. Soc. · 2003 · 125 · 1394010.1021/ja029267j ↗
20. Schulz-Dobrick M. · J. Am. Chem. Soc. · 2005 · 127 · 1281610.1021/ja054734t ↗
21. Hu B. · J. Phys. Chem. C · 2008 · 112 · 1116910.1021/jp801267j ↗
22. García-Serrano J. · Chem. Mater. · 2008 · 20 · 514610.1021/cm703201d ↗
23. Nadagouda M. N. · Cryst. Growth Des. · 2008 · 8 · 29110.1021/cg070473i ↗
24. Nadagouda M. N. · Cryst. Growth Des. · 2007 · 7 · 68610.1021/cg070554e ↗
25. Nadagouda M. N. · Cryst. Growth Des. · 2007 · 7 · 258210.1021/cg070554e ↗
26. Choi H. · Chem. Mater. · 2006 · 18 · 537710.1021/cm0615626 ↗
27. Nadagouda M. N. · Green Chem. · 2006 · 8 · 51610.1039/b601271j ↗
28. Baruwati B. · J. Phys. Chem. C · 2008 · 112 · 1839910.1021/jp807245g ↗
29. Polshettiwar V. · Chem. Commun. · 2008 · 631810.1039/b814715a ↗
30. Polshettiwar V. · Chem.—Eur. J. · 2009 · 15 · 158210.1002/chem.200802264 ↗
31. Polshettiwar V. · Org. Biol. Chem. · 2009 · 7 · 3710.1039/B817669H ↗
32. Polshettiwar V. · Green. Chem. · 2009 · 11 · 12710.1039/B815058C ↗
33. Millstone J. E. · J. Am. Chem. Soc. · 2005 · 127 · 531210.1021/ja043245a ↗
34. Kelly K. L. · J. Phys. Chem. B · 2003 · 107 · 66810.1021/jp026731y ↗