journal article·2011-02-22

Tuning Chemical Enhancement of SERS by Controlling the Chemical Reduction of Graphene Oxide Nanosheets

Xinxin Yu, Hongbing Cai, Wenhua Zhang, Xinjing Li, Nan Pan, Yi Luo, Xiaoping Wang, J. G. Hou

ACS Nano· Volume 5· Issue 2
Publisher page

Abstract

Chemical enhancement is an important mechanism in surface-enhanced Raman spectroscopy. It is found that mildly reduced graphene oxide (MR-GO) nanosheets can significantly increase the chemical enhancement of the main peaks by up to 1 order of magnitude for adsorbed Rhodamine B (RhB) molecules, in comparison with the mechanically exfoliated graphene. The observed enhancement factors can be as large as ∼10(3) and show clear dependence on the reduction time of graphene oxide, indicating that the chemical enhancement can be steadily controlled by specific chemical groups. With the help of X-ray photoelectron spectra, these chemical species are identified and the origin of the observed large chemical enhancement can thus be revealed. It is shown that the highly electronegative oxygen species, which can introduce a strong local electric field on the adsorbed molecules, are responsible for the large enhancement. In contrast, the local defects generated by the chemical reduction show no positive correlation with the enhancement. Most importantly, the dramatically enhanced Raman spectra of RhB molecules on MR-GO nanosheets reproduce all important spectral fingerprints of the molecule with a negligible frequency shift. Such a unique noninvasive feature, along with the other intrinsic advantages, such as low cost, light weight, easy availability, and flexibility, makes the MR-GO nanosheets very attractive to a variety of practical applications.
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Research context

OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Nanocluster Synthesis and Applications · Nonlinear Optical Materials Studies

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

Affiliations

Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China

Department of Physics, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China

Department of Chemical Physics, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China

References (38)

Show source-provided references
1. Wu J. S. · Chem. Rev. · 2007 · 107 · 71810.1021/cr068010r ↗
2. Verma V. P. · Appl. Phys. Lett. · 2010 · 96 · 20310810.1063/1.3431630 ↗
3. Bunch J. S. · Science · 2007 · 315 · 49010.1126/science.1136836 ↗
4. Ling X. · Nano Lett. · 2010 · 10 · 55310.1021/nl903414x ↗
5. Xie L. M. · J. Am. Chem. Soc. · 2009 · 131 · 989010.1021/ja9037593 ↗
6. Sun Y. H. · Nano Lett. · 2010 · 10 · 174710.1021/nl100170j ↗
7. Shen X. S. · Phys. Chem. Chem. Phys. · 2009 · 11 · 745010.1039/b904712c ↗
8. Nielsen P. · J. Phys. Chem. C · 2009 · 113 · 1416510.1021/jp9039012 ↗
9. Stiles P. L. · Annu. Rev. Anal. Chem. · 2008 · 1 · 60110.1146/annurev.anchem.1.031207.112814 ↗
10. Polavarapu L. · Langmuir · 2008 · 24 · 1060810.1021/la802319c ↗
11. Wang L. F. · Ind. Eng. Chem. Res. · 2009 · 48 · 292010.1021/ie8014507 ↗
12. Goncalves G. · Chem. Mater. · 2009 · 21 · 479610.1021/cm901052s ↗
13. Lu C. H. · Angew. Chem., Int. Ed. · 2009 · 48 · 478510.1002/anie.200901479 ↗
14. Liu Z. · J. Am. Chem. Soc. · 2008 · 130 · 1087610.1021/ja803688x ↗
15. Wang L. · ACS Nano · 2009 · 3 · 299510.1021/nn900667s ↗
16. Hu Z. L. · Langmuir · 2010 · 26 · 668110.1021/la9040166 ↗
17. Otto A. · J. Raman Spectrosc. · 2005 · 36 · 49710.1002/jrs.1355 ↗
18. Jensen L. · Chem. Soc. Rev. · 2008 · 37 · 106110.1039/b706023h ↗
19. Lombardi J. R. · J. Phys. Chem. C · 2008 · 112 · 560510.1021/jp800167v ↗
20. Eda G. · Adv. Mater. · 2010 · 22 · 50510.1002/adma.200901996 ↗
21. Luo Z. T. · J. Am. Chem. Soc. · 2009 · 131 · 89810.1021/ja807934n ↗
22. Dreyer D. R. · Chem. Soc. Rev. · 2010 · 39 · 22810.1039/B917103G ↗
23. Si Y. · Nano Lett. · 2008 · 8 · 167910.1021/nl080604h ↗
24. Gomez-Navarro C. · Nano Lett. · 2007 · 7 · 349910.1021/nl072090c ↗
25. Albrecht A. C. · J. Chem. Phys. · 1971 · 55 · 443810.1063/1.1676771 ↗
26. Sariciftcia N. S. · Synth. Met. · 1994 · 62 · 10710.1016/0379-6779(94)90300-X ↗
27. Zhang W. H. · J. Chem. Phys. · 2009 · 131 · 24450510.1063/1.3276339 ↗
28. Benayad A. · Chem. Phys. Lett. · 2009 · 475 · 9110.1016/j.cplett.2009.05.023 ↗
29. Tung V. C. · Nat. Nanotechnol. · 2009 · 4 · 2510.1038/nnano.2008.329 ↗
30. Stankovich S. · J. Mater. Chem. · 2006 · 16 · 15510.1039/B512799H ↗
31. Böttcher, C. J. F.InTheory of Electric Polarization;Böttcher, C. J. F., Ed.Elsevier:Amsterdam, 1973; pp17−26.
32. Zhang J. T. · J. Phys. Chem. B · 2005 · 109 · 1254410.1021/jp050471d ↗
33. Hildebrandt P. · J. Phys. Chem. · 1984 · 88 · 593510.1021/j150668a038 ↗
34. Li J. F. · Nature · 2010 · 464 · 39210.1038/nature08907 ↗
35. Yang X. Y. · J. Phys. Chem. C · 2008 · 112 · 1755410.1021/jp806751k ↗
36. Novoselov K. S. · Nature · 2005 · 438 · 19710.1038/nature04233 ↗
37. Novoselov K. S. · Science · 2004 · 306 · 66610.1126/science.1102896 ↗
38. Gilje S. · Nano Lett. · 2007 · 7 · 339410.1021/nl0717715 ↗