Environmental Research Laboratory, School of Science and Engineering, Kinki University, 3-4-1, Kowakae, Higashi-Osaka, Osaka 577-8502, Japan.
Langmuir. 2011 Aug 16;27(16):10334-9. doi: 10.1021/la2016935. Epub 2011 Jul 21.
Visible-light irradiation to monoclinic scheelite BiVO(4) (m-BiVO(4)) in a solution of copper acetylacetonate (Cu(acac)(2)) has led to its decomposition and Cu recovery. The photonic efficiency at λ = 440 ± 15 nm reaches 3.4%, exceeding the value for the TiO(2)-photocatalyzed reaction at λ = 355 ± 23 nm (2.0%). The adsorption isotherm and the light intensity-dependence of the decomposition rate indicate high adsorptivity of m-BiVO(4) for Cu(acac)(2) or its sufficient supply to the surface reaction sites, which mainly contributes to the high photocatalytic activity. Electrochemical measurements using cyclic voltammetry suggest that the reaction proceeds via the oxidative degradation of the ligand followed by the reduction of the resulting Cu(2+) ions. Under aerobic conditions, the Cu(2+) ions mediate the electron transfer from the conduction band of m-BiVO(4) to O(2) to complete the catalytic cycle.
可见光辐照在乙酰丙酮铜(Cu(acac)(2))溶液中的单斜白钨矿 BiVO(4)(m-BiVO(4))导致其分解和 Cu 的回收。在 λ = 440 ± 15 nm 处的光量子效率达到 3.4%,超过了 λ = 355 ± 23 nm(2.0%)处的 TiO(2)-光催化反应的值。吸附等温线和分解速率的光强依赖性表明 m-BiVO(4)对 Cu(acac)(2)具有高吸附性或其对表面反应位点的充分供应,这主要有助于高光催化活性。使用循环伏安法的电化学测量表明,反应通过配体的氧化降解进行,然后是生成的 Cu(2+)离子的还原。在有氧条件下,Cu(2+)离子介导从 m-BiVO(4)的导带到 O(2)的电子转移,以完成催化循环。