Wang Qi, Zhang Chenlu, Wu Hong, Gao Qiaoyuan, Duan Ran, Chen Chuncheng
School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018, China.
School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018, China.
J Colloid Interface Sci. 2019 Jul 1;547:1-13. doi: 10.1016/j.jcis.2019.03.088. Epub 2019 Mar 26.
BiOCO was co-decorated by β-phase AgI and BiO forming visible-light-active AgI(β)/BiO(β)-BiOCO composite via simply calcining AgI/BiOCO. The calcination temperature and time played vital role in regulating the structure as well as photocatalytic performance. Optimal AgI(β)/BiO(β)-BiOCO was obtained after 325 C calcination for 2 h with 5% AgI. The ratio of BiO to BiOCO was estimated to be ca. 3:1 on the catalyst surface. The transformation process for n-type BiOCO to p-type BiO(β) was monitored and verified by flat band potential measurements. Due to the presence of p-n junctions between p-type BiO(β), n-type AgI(β) and BiOCO, the optimized ternary composite displayed enhanced photocurrent density and reduced charge transfer resistance, which were beneficial for photocatalytic applications. Despite of decreased specific surface area, dramatically enhanced photocatalytic performance can be observed for simultaneous removal of Cr(VI) and phenol. For example, the estimated k and k on AgI(β)/BiO(β)-BiOCO were 3.3 and 2.2 times relative to those on uncalcined AgI/BiOCO, respectively. The optimized composite also displayed good stability in 4 successive cyclic runs.
通过简单煅烧AgI/BiOCO,β相AgI和BiO对BiOCO进行共修饰,形成可见光活性的AgI(β)/BiO(β)-BiOCO复合材料。煅烧温度和时间在调节结构以及光催化性能方面起着至关重要的作用。用5%的AgI在325℃煅烧2小时后得到了最佳的AgI(β)/BiO(β)-BiOCO。催化剂表面BiO与BiOCO的比例估计约为3:1。通过平带电位测量监测并验证了n型BiOCO向p型BiO(β)的转变过程。由于p型BiO(β)、n型AgI(β)和BiOCO之间存在p-n结,优化后的三元复合材料显示出增强的光电流密度和降低的电荷转移电阻,这有利于光催化应用。尽管比表面积有所降低,但对于同时去除Cr(VI)和苯酚,可以观察到光催化性能显著增强。例如,AgI(β)/BiO(β)-BiOCO上估计的k和k分别是未煅烧的AgI/BiOCO上的3.3倍和2.2倍。优化后的复合材料在4次连续循环运行中也表现出良好的稳定性。