journal article·2008-12

pH-dependent 2-amino-5-mercapto-1,3,4-thiadiazole monolayers at the silver surface: Surface enhanced Raman scattering spectroscopic and electrochemical observations

Haifeng Yang, Wei Song, Jiahua Ji, Xuan Zhu, Yiping Sun, Renyan Yang, Zongrang Zhang

Applied Surface Science· Volume 255· Issue 5
Publisher page

Abstract

Abstract The pH-dependent structures of the 2-amino-5-mercapto-1,3,4-thiadiazole (AMT) self-assembled monolayers (SAMs) on the silver surface were studied by surface enhanced Raman scattering (SERS) spectroscopy. The resulting SERS spectra show that the adsorption fashion of AMT monolayers formed at pH 1 could exhibit the strongest interaction with the silver surface among the investigated pH values at 1, 7, and 13. Electrochemical impedance spectroscopy (EIS) illuminates that the anticorrosive effect of AMT monolayers formed under pH 1 is the best. The inhibition efficiencies of AMT SAMs formed under pH 1, 7 and 13 are 72.2, 39.1 and 4.97%, respectively, according to experimental results of their Tafel plots.
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Research context

OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Molecular Junctions and Nanostructures · Advanced biosensing and bioanalysis techniques

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

References (30)

Show source-provided references
1. Ganorkar · Stud. Conserv. · 1988 · 33 · 9710.2307/1506307 ↗
2. Bastidas · Mater. Corros. · 1996 · 47 · 33310.1002/maco.19960470606 ↗
3. Otero · Mater. Corros. · 1996 · 47 · 13310.1002/maco.19960470303 ↗
4. Pandit · Trans. SAEST · 1992 · 7 · 222
5. Gajendragad · Indian J. Chem. · 1975 · 13 · 1331
6. Gajendragad · Chem. Soc. Jpn. · 1975 · 48 · 102410.1246/bcsj.48.1024 ↗
7. Downie · Acta Crystallogr. B · 1972 · 28 · 158410.1107/S0567740872004625 ↗
8. Edwards · Mol. Struct. · 1995 · 351 · 5110.1016/0022-2860(94)08485-Z ↗
9. Prado · Non-Cryst. Solids · 2004 · 333 · 6110.1016/j.jnoncrysol.2003.09.053 ↗
10. Nie · Science · 1997 · 275 · 110210.1126/science.275.5303.1102 ↗
11. Kneipp · Phys. Rev. Lett. · 1997 · 78 · 166710.1103/PhysRevLett.78.1667 ↗
12. Goulet · Anal. Chem. · 2007 · 79 · 272810.1021/ac062059f ↗
13. Shafer-Peltier · J. Am. Chem. Soc. · 2003 · 125 · 58810.1021/ja028255v ↗
14. Cao · Science · 2002 · 297 · 153610.1126/science.297.5586.1536 ↗
15. Premasiri · J. Raman Spectrosc. · 2001 · 32 · 91910.1002/jrs.762 ↗
16. Ringler · Nano Lett. · 2007 · 9 · 275310.1021/nl0712466 ↗
17. Bukowska · J. Mol. Struct. · 1992 · 275 · 15110.1016/0022-2860(92)80191-J ↗
18. Chowdhury · Spectrochim. Acta A · 2000 · 56 · 210710.1016/S1386-1425(00)00263-8 ↗
19. Diao · Electroanal. Chem. · 2001 · 495 · 9810.1016/S0022-0728(00)00424-1 ↗
20. Cui · J. Electroanal. Chem. · 1999 · 470 · 910.1016/S0022-0728(99)00201-6 ↗
21. Janek · J. Phys. Chem. B · 1997 · 101 · 855010.1021/jp971698e ↗
22. Boubour · J. Phys. Chem. B · 2000 · 104 · 900410.1021/jp000151o ↗
23. Taniguchi · J. Electroanal. Chem. · 1986 · 202 · 1510.1016/0022-0728(86)90127-0 ↗
24. Yang · J. Phys. Chem. C · 2007 · 111 · 798610.1021/jp070439e ↗
25. Allen · Chem. Phys. Lett. · 1979 · 63 · 45510.1016/0009-2614(79)80688-0 ↗
26. Gao · J. Phys. Chem. · 1990 · 94 · 685810.1021/j100380a059 ↗
27. Moskovitz · J. Phys. Chem. · 1990 · 88 · 1986
28. Wrzosek · J. Phys. Chem. C · 2007 · 111 · 1739710.1021/jp075442c ↗
29. Roman · J. Pharm. Biomed. Anal. · 1998 · 18 · 13710.1016/S0731-7085(98)00154-X ↗
30. Bockris · 1993