4.7 Article

SERS active Ag encapsulated Fe@SiO2 nanorods in electromagnetic wave absorption and crystal violet detection

Journal

ENVIRONMENTAL RESEARCH
Volume 135, Issue -, Pages 95-104

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2014.08.026

Keywords

Electromagnetic wave; SERS; Nanorods; Carcinogenic dye; Crystal violet

Funding

  1. DRDO [ERIP/ER/ \1000384/M/01/1271]
  2. CSIR [09/081(1007)/2009-EMR-I]

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The present work is focused on the preparation of Fe nanorods by the chemical reduction of FeCI3 (aq) using NaBH4 in the presence of glycerol as template followed by annealing of the product at 500 degrees C in the presence of H-2 gas flow. Subsequently, its surface has been modified by silica followed by silver nanoparticles to form silica coated Fe (Fe@SiO2) and Ag encapsulated Fe@SiO2 nanostructure employing the Stober method and silver mirror reaction respectively. XRD pattern of the products confirmed the formation of bcc phase of iron and fcc phase of silver, though silica remained amorphous. FESEM images established the growth of iron nanorods from the annealed product and also formation of silica and silver coating on its surface. The appearance of the characteristics bands in FTIR confirmed the presence of SiO2 on the Fe surface. Magnetic measurements at room temperature indicated the ferromagnetic behavior of as prepared iron nanorods, Fe@SiO2 and silver encapsulated Fe@SiO2 nanostructures. All the samples exhibited strong microwave absorption property in the high frequency range (10 GHz), though it is superior for Ag encapsulated Fe@SiO2 (-14.7 dB) compared with Fe@SiO2 (- 9.7 dB) nanostructures of the same thickness. The synthesized Ag encapsulated Fe@SiO2 nanostructure also exhibited the SERS phenomena, which is useful in the detection of the carcinogenic dye crystal violet (CV) upto the concentration of 10(-10) M. All these findings clearly demonstrate that the Ag encapsulated Fe@SiO2 nanostructure could efficiently be used in the environmental remediation. (C) 2014 Elsevier Inc. All rights reserved.

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