阴极
阳极
二氧化钛
氧化剂
柠檬酸
钛
化学
光催化
薄膜
电子转移
金属
费米能级
材料科学
无机化学
电子
纳米技术
电极
冶金
光化学
催化作用
物理化学
物理
量子力学
生物化学
有机化学
作者
Han Song,Jing Shang,Junhui Ye,Qian Li
标识
DOI:10.1016/j.tsf.2013.12.002
摘要
Photocatalytic and photoelectrocatalytic (PEC) reductions of Cr(VI) based on TiO2 thin films were investigated under various conditions. Photogenerated electrons transferred from TiO2 thin film to cathode can contribute to PEC reduction of Cr(VI) only when the Fermi level of cathode lies above the chemical potential of Cr(VI), almost independent on the applied voltage of the direct current. In addition, the TiO2-coated anode is the major site that accommodates the PEC reduction of Cr(VI) with hole scavenger citric acid, regardless of the Fermi level of the cathode. Although electron transfer from TiO2 to Cr(VI) is an exothermic process, the photogenerated holes in TiO2 can markedly hamper Cr(VI) reduction over the TiO2 thin film by oxidizing the lower-valence Cr back to Cr(VI), which may be counteracted by the citric acid. This research provides some in-depth insights on developing photocatalysts which enable highly efficient PEC reduction of Cr(VI) in the future.
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