4.6 Article

To dimerize or not: para-aminothiophenol on a bismuth heterostructure

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 25, Issue 13, Pages 9569-9575

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cp05918e

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This study investigated the surface enhanced Raman spectroscopy (SERS) of p-aminothiophenol (PATP) on beta-Bi2O3/Bi2O2CO3 nanoparticles. It was found that no transformation of PATP to p,p'-dimercaptoazobenzene (DMAB) occurred on beta-Bi2O3/Bi2O2CO3 nanoparticles, unlike on noble metal surfaces. Density functional theory (DFT) calculations supported the experimental results and revealed the charge transfer direction from PATP to beta-Bi2O3/Bi2O2CO3 nanoparticles.
Surface enhanced Raman spectroscopy (SERS) of p-aminothiophenol (PATP) was investigated on beta-Bi2O3/Bi2O2CO3 nanoparticles, a novel bismuth based metal substrate with the lowest limit of detection of 1 mM. Unlike on noble metal surfaces where PATP gets converted to p,p '-dimercaptoazobenzene (DMAB) due to photocatalytic coupling, no such transformation of PATP was observed on beta-Bi2O3/Bi2O2CO3 nanoparticles. Density functional theory (DFT) calculations at the PW91PW91/LANL2DZ/6-311+G(d,p) level of theory supported the experimental results exceedingly well. Also, the charge transfer direction from PATP to beta-Bi2O3/Bi2O2CO3 nanoparticles was revealed by the projected density of states calculation.

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