光催化
高分辨率透射电子显微镜
甲基橙
扫描电子显微镜
材料科学
透射电子显微镜
异质结
光致发光
化学工程
对苯二甲酸
光化学
分析化学(期刊)
核化学
催化作用
纳米技术
化学
光电子学
有机化学
复合材料
工程类
聚酯纤维
作者
Jing Cao,Benyan Xu,Haili Lin,Bangde Luo,Shifu Chen
标识
DOI:10.1016/j.cej.2012.01.035
摘要
BiOI/BiOBr heterostructures, synthesized by a simple chemical etching method using acetic acid and KI as etching agents to react with BiOBr particles, were characterized by X-ray powder diffraction (XRD), UV–vis diffuse reflectance spectra (UV–vis DRS), scanning electron microscope (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM) and Brunauer-Emmett-Teller (BET) surface area. The as-prepared samples exhibited more efficient photocatalytic activities than pure BiOI and BiOBr for the degradation of methyl orange (MO) under visible light irradiation (λ > 420 nm), which could be attributed to the efficient separation of electron–hole pairs caused by the formation of BiOI–BiOBr heterojunction. Terephthalic acid photoluminescence (TA-PL) probing test and radical scavenger's experiments demonstrated that h+, O2− and H2O2 were the dominant reactive species while OH could be negligible. A possible transfer process of photogenerated carriers was proposed based on the band structures of BiOI and BiOBr
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