Skip to main navigation Skip to search Skip to main content

Direct evidence for conversion of p-aminothiophenol to p,p'- dimercaptoazobenzene by in situ reduplicative surface-enhanced Raman scattering measurements

  • Beijing Institute of Technology
  • Beihang University

Research output: Contribution to journalArticlepeer-review

Abstract

There has been a surge of interest in the surface-enhanced Raman scattering (SERS) of p-aminothiophenol (PATP), since its SERS spectra are dependent on the measurement conditions. However, there is a dispute over the origin of the so-called b2 modes in SERS spectrum of PATP recently. Some researchers propose that these bands come from selective chemical enhancement, while others conclude that these bands are due to the ag modes of p,p'-dimercaptoazobenzene (DMAB) produced from PATP by surface photoreaction. To solve this problem, we have studied the SERS spectra of PATP on Au and Ag nanoparticles by in situ measurement under various conditions. The results proved that the b2 modes are not due to PATP but due to the a g modes of DMAB. The key of the method is to ensure the SERS spectra taken from the same point in reduplicative measurements. The result showed that the stable SERS spectrum of PATP was essentially from DMAB. The reversibility of the PATP SERS spectra in previous studies is due to the variety of the measurement points, which is in nature of different PATP conversions to DMAB under different conditions.

Original languageEnglish
Pages (from-to)1200-1203
Number of pages4
JournalJournal of Raman Spectroscopy
Volume44
Issue number8
DOIs
StatePublished - Aug 2013

Keywords

  • p,p'-dimercaptoazobenzene
  • p-aminothiophenol
  • surface photoreaction
  • surface-enhanced Raman scattering (SERS)

Fingerprint

Dive into the research topics of 'Direct evidence for conversion of p-aminothiophenol to p,p'- dimercaptoazobenzene by in situ reduplicative surface-enhanced Raman scattering measurements'. Together they form a unique fingerprint.

Cite this