Journal
ELECTROCHIMICA ACTA
Volume 369, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2020.137655
Keywords
Vitamin B-12; Electrocatalysis; Electro-dehalogenation; Halohydrocarbons; Surface Active Ionic Liquid
Categories
Funding
- Department of Science and Technology
- New Delhi, India [SR/S1/PC-11/2009]
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The study demonstrates that aqueous micellar solutions can significantly enhance the electrocatalytic efficiency of VB12 for electroreduction reactions. By employing extensive voltammetric investigations, it was found that the enhancement can reach up to several thousand to tens of thousands times. This finding is of great importance for eco-friendly electro-detoxification of water insoluble halocarbons in aqueous phase.
Vitamin B-12 (VB12) is considered as a promising molecular catalyst for a diverse range of important industrial, synthetic and environmental electrochemical transformations. However, the low turnover frequency (TOF) and the solubility concerns pose serious challenges in harnessing the electrocatalytic potential of VB12 for these applications. Herein, we demonstrate that aqueous micellar solutions of SAILs viz. 1-dodecyl-3-methylimidazolium chloride ([DDMIM][Cl]) and 1-butyl-3-methylimidazolium dodecyl sulfate ([BMIM][DS]) enhance by several orders the electrocatalytic efficiency of VB12 toward electroreduction of bromoacetonitrile. Our extensive voltammetric investigations, as recommended for the benchmarking of molecular catalysts, viz. Foot of Wave Analysis, catalytic Tafel plots and the resulting estimates of electrocatalytic parameters like TOF and TOF at zero overpotential, clearly establish that [DDMIM][Cl] and [BMIM][DS] micellar solutions enhance the electrocatalytic performance of VB12 by 10(6) and 10(4) times respectively. The presented study is of significant importance in light of some recent reports that have demonstrated the aptness of aqueous SAIL micellar solutions for aqueous phase eco-green electro-detoxification of water insoluble halocarbons. (C) 2020 Elsevier Ltd. All rights reserved.
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