A photoelectrocatalytic (PEC) system for the decomposition of Ag-cyanide complexes synchronously with Ag recovery was established using the titanium dioxide nanorods (TiO2 NRs) as photoanode and the titanium plate as… Click to show full abstract
A photoelectrocatalytic (PEC) system for the decomposition of Ag-cyanide complexes synchronously with Ag recovery was established using the titanium dioxide nanorods (TiO2 NRs) as photoanode and the titanium plate as cathode. The removal efficiency of total cyanide was 76.58%, and the recovery ratio of Ag achieved 84.48% at the applied bias potential of 1.0 V vs SCE in the PEC process. During the reaction, the surface variations and photo-electric properties of TiO2 NRs photoanode or titanium cathode were characterized by SEM-EDS, XPS, and photoelectronic analyses. It was indicated that Ag2O and metallic Ag were deposited onto the TiO2 NRs photoanode and titanium cathode, respectively. Specifically, the in situ generated Ag2O on the TiO2 NRs photoanode facilitated the separation of the photogenerated charge carriers and enhanced the visible-light response, thus improving its PEC catalytic activity toward cyanide destruction. Combined with the results of active species quenching experiments, the mechanism of Ag-cyanide complexes decomposition and metallic Ag recovery by the PEC process was proposed.
               
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