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SERS Enhancement on the Basis of Temperature‐Dependent Chemisorption: Microcalorimetric Evidence
Author(s) -
Roy Chandra Nath,
Ghosh Debasmita,
Mondal Somrita,
Kundu Somashree,
Maiti Susmita,
Saha Abhijit
Publication year - 2016
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201600941
Subject(s) - rhodamine 6g , raman spectroscopy , chemisorption , chemistry , surface enhanced raman spectroscopy , analytical chemistry (journal) , crystal violet , raman scattering , adsorption , molecule , isothermal titration calorimetry , substrate (aquarium) , isothermal process , photochemistry , optics , organic chemistry , thermodynamics , medicine , physics , oceanography , pathology , geology
The mechanism of surface‐enhanced Raman spectroscopy (SERS) is not very clear in view of the magnitude of the contribution of electromagnetic factor as well as the chemical mechanism. This report presents the extent of adsorption at different temperatures in terms of signal enhancements in SERS employing silver nanoparticles (AgNPs) of various shapes as substrate and dye molecules, crystal violet or Rhodamine 6G, as model Raman probes. Initially, the SERS signal increases with increasing temperature until a maximum intensity is reached, before it gradually decreases with increasing temperature. This trend is independent of the shape of the Raman substrates and probes. However, the temperature at which maximum intensity is obtained may depend upon the nature of the Raman probe. The energetics involved in the chemisorption process between dye molecules and AgNPs were determined through isothermal titration calorimetry and their implications for the observed SERS signals were assessed. The maximum heat change occurred at the temperature at which the maximum signal enhancement in SERS was obtained and the enhanced interaction at optimum temperature was confirmed by absorption spectroscopy.