Spectrophotometric evaluation of surface morphology dependent catalytic activity of biosynthesized silver and gold nanoparticles using UV-vis spectra: A comparative kinetic study

被引:32
作者
Ankamwar, Balaprasad [1 ]
Kamble, Vaishali [1 ]
Sur, Ujjal Kumar [1 ]
Santra, Chittaranjan [2 ]
机构
[1] Savitribai Phule Pune Univ, Dept Chem, Bioinspired Mat Res Lab, Pune 411007, Maharashtra, India
[2] Netaji Nagar Day Coll, Dept Chem, Regent Pk, Kolkata 700092, India
关键词
Nanoparticles; Surface morphology; 4-Nitrophenol; Catalytic activity; Pseudo-first order reaction; Surface-enhanced Raman scattering; ONE-STEP SYNTHESIS; LEAF EXTRACT; REDUCTION; MODEL;
D O I
10.1016/j.apsusc.2016.01.093
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The development of eco-friendly and cost-effective synthetic protocol for the preparation of nanomaterials, especially metal nanoparticles is an emerging area of research in nanotechnology. These metal nanoparticles, especially silver can play a crucial role in various catalytic reactions. The biosynthesized silver nanoparticles described here was very stable up to 6 months and can be further exploited as an effective catalyst in the chemical reduction of 4-nitrophenol to 4-aminophenol. The silver nanoparticles were utilized as an efficient surface-enhanced Raman scattering (SERS) active substrate using Rhodamine 6G as Raman probe molecule. We have also carried out systematic comparative studies on the catalytic efficiency of both silver and gold nanoparticles using UV-vis spectra to monitor the above reaction spectrophotometrically. We find that the reaction follows pseudo-first order kinetics and the catalytic activity can be explained by a simple model based on Langmuir-Hinshelwood mechanism for heterogeneous catalysis. We also find that silver nanoparticles are more efficient as a catalyst compare to gold nanoparticles in the reduction of 4-nitrophenol to 4-aminophenol, which can be explained by the morphology of the nanoparticles as determined by transmission electron microscopy. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:275 / 283
页数:9
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