Iodine adlayer mediated gold electrooxidation in bis(trifluoromethylsulfonyl)amide-based ionic liquids

Abstract

Conventional complexing ligands for the wet etching of gold are hazardous, making large-scale utilization problematic. In particular, the environmental risks caused by these materials must be minimized. To address this problem, an electrochemical etching method for gold using bis(trifluoromethylsulfonyl)amide ([Tf2N]–)-based ionic liquids (ILs) has been developed. Here, only one layer of conventional complexing ligand, that is, iodine on gold, is required to achieve the continuous dissolution of gold under a positive electrode potential. In addition, the etching behavior involves sacrificial anode electrolysis (SAE) to generate gold nanoparticles (AuNPs). It was found that the electrochemical oxidation of gold is strongly dependent upon the type of halide ion, and the iodine-modified gold electrode produced a large oxidation peak in [Tf2N]–-based ILs. The voltammetric profiles of iodine-modified gold electrodes reveal that the electronic charge consumed during the electrochemical oxidation is affected by the IL cation and the crystallographic orientation of gold, increasing as ammonium < imidazolium < pyrrolidinium and Au(111) < Au(100) < Au(110), respectively. Of the IL anions evaluated in this study, the apparent oxidation peak was only observed for iodine-modified gold electrode in [Tf2N]–-based ILs, suggesting that [Tf2N]– anions promote gold complexation and act as ligands. Further, microscopic and spectroscopic measurements provide evidence of gold dissolution after electrochemical oxidation and the formation of gold complexes, followed by the generation of AuNPs. The results reveal a mechanism for the iodine-catalyzed electrochemical oxidation of gold in [Tf2N]–-based ILs. The electrolysis of gold in the ILs reported here opens avenues for acquiring novel aurate salts with IL anions and AuNPs.