Zhao Xu, Zhu Yongfa
Department of Chemistry, Tsinghua University, Beijing, 100084, People's Republic of China.
Environ Sci Technol. 2006 May 15;40(10):3367-72. doi: 10.1021/es052029e.
Synergetic degradation of rhodamine B (RhB) was investigated by combining electro-oxidation and photocatalysis using porous ZnWO4 film at various bias potentials. The applied bias potential below 0.8 V enhanced the photocatalytic degradation of RhB by promoting the separation and transfer of photogenerated holes and electrons. At the potential between 0.8 and 1.0 V, the degradation of RhB was further enhanced, which is induced by direct electro-oxidation and photocatalysis. At the potential greater than 1.3 V, indirect electro-oxidation of RhB occurred with the largest synergetic effect. The synergetic effect can also increase the mineralization degree of the RhB. On the basis of the X-ray photoelectron spectra (XPS) analysis of the surface of the electrode after electrochemical reaction, the electropolymerization occurred which blocked the electrode and slowed the electro-oxidation of RhB. Active species generated via the photocatalytic process can activate the passivated electrode and promote the electro-oxidation of RhB. The O2 electrochemically generated at the anode promoted the photocatalysis by capturing the photogenerated electrons and may induce the formation of H2O2. Thus, more active species could be formed through new reactive routines in the photoelectrocatalytic (PEC) process. RhB degradation was mainlythrough decomposition of the conjugated chromophore structure with slight occurrence of de-ethylation. The stability of the electrode in the PEC process was confirmed based on the XPS and Raman analysis.
通过在不同偏置电位下使用多孔ZnWO4薄膜将电氧化与光催化相结合,研究了罗丹明B(RhB)的协同降解。低于0.8 V的外加偏置电位通过促进光生空穴和电子的分离与转移,增强了RhB的光催化降解。在0.8至1.0 V的电位下,RhB的降解进一步增强,这是由直接电氧化和光催化引起的。在大于1.3 V的电位下,发生了RhB的间接电氧化,协同效应最大。协同效应还可以提高RhB的矿化程度。根据电化学反应后电极表面的X射线光电子能谱(XPS)分析,发生了电聚合,这阻塞了电极并减缓了RhB的电氧化。通过光催化过程产生的活性物种可以激活钝化的电极并促进RhB的电氧化。在阳极电化学产生的O2通过捕获光生电子促进了光催化,并可能诱导H2O2的形成。因此,在光电催化(PEC)过程中可以通过新的反应途径形成更多的活性物种。RhB的降解主要是通过共轭发色团结构的分解,脱乙基反应轻微发生。基于XPS和拉曼分析,证实了电极在PEC过程中的稳定性。