Abstract

Electrocatalysis using low-cost materials is a promising, economical strategy for remediation of water contaminated with organic chemicals and microorganisms. Here, we report the use of iron phosphide (Fe2P) precatalyst for electrocatalytic water oxidation; degradation of a representative aromatic hydrocarbon, the dye rhodamine B (RhB); and inactivation of Escherichia coli (E. coli) bacteria. It was found that during anodic oxidation, the Fe2P phase was converted to iron phosphate phase (Fe2P-iron phosphate). This is the first report that Fe2P precatalyst can efficiently catalyze electrooxidation of an organic molecule and inactivate microorganisms in aqueous media. Using a thin film of Fe2P precatalyst, we achieved 98% RhB degradation efficiency and 100% E. coli inactivation under an applied bias of 2.0 V vs. reversible hydrogen electrode in the presence of in situ generated reactive chlorine species. Recycling test revealed that Fe2P precatalyst exhibits excellent activity and reproducibility during degradation of RhB. High-performance liquid chromatography with UV-Vis detection further confirmed the electrocatalytic (EC) degradation of the dye. Finally, in tests using Lepidium sativum L., EC-treated RhB solutions showed significantly diminished phytotoxicity when compared to untreated RhB. These findings suggest that Fe2P-iron phosphate electrocatalyst could be an effective water remediation agent.

Highlights

  • Electrochemical oxidation has emerged as a promising means of eliminating contaminants from water [1]

  • We report for the first time the transformation of Fe2P into iron phosphate during EC degradation of rhodamine B (RhB) dye (98%) and inactivation of E. coli bacteria (100%)

  • Under the experimental conditions, Cl− ions are oxidized to hypochlorous acid (HClO), which plays an essential role in the water treatment process

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Summary

Introduction

Electrochemical oxidation has emerged as a promising means of eliminating contaminants from water [1]. The standard potential for the Cl2 evolution (Cl−/Cl2 1.36 V vs. normal hydrogen electrode (NHE)) is relatively low, making it an attractive option for efficient electrochemical wastewater treatment [19]

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