纳米棒
阴极
氰化物
二氧化钛
钛
X射线光电子能谱
材料科学
金属
化学工程
分解
降级(电信)
无机化学
化学
纳米技术
冶金
有机化学
物理化学
工程类
电信
计算机科学
作者
Ran Mao,Di Song,Yan Wang,Xu Zhao
出处
期刊:Chemosphere
[Elsevier BV]
日期:2019-10-22
卷期号:242: 125156-125156
被引量:19
标识
DOI:10.1016/j.chemosphere.2019.125156
摘要
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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