Jiang Qi, Ji Mengxia, Chen Rong, Zhang Yi, Li Kai, Meng Chenxi, Chen Zhigang, Li Huaming, Xia Jiexiang
School of the Environment and Safety Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, PR China.
School of Chemistry and Chemical Engineering, Institute for Energy Research, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, PR China.
J Colloid Interface Sci. 2020 Aug 15;574:131-139. doi: 10.1016/j.jcis.2020.04.018. Epub 2020 Apr 7.
Ultrathin BiOBr nanosheets have been prepared via an ionic liquid induced mechanochemical synthesis method at ambient temperature for the first time using 1-hexadecyl-3-methy-limidazolium bromine ([Cmim]Br). Transmission electron microscope and atomic force microscope images show that the ultrathin BiOBr nanosheets possessed an average diameter of approximately 200-300 nm with a thickness of 3-4 nm. For comparison, KBr was selected as Br source for the preparation of BiOBr nanosheets and the experimental results demonstrate that the ionic liquid and mechanical ball milling method had a significant impact on the fabrication of nanosheet structures. Compared with the as-prepared control samples, the ultrathin BiOBr nanosheet photocatalyst exhibited significantly increased photocatalytic performance for the removal of organic pollutants. A possible mechanism for this enhanced activity was proposed based on the shorter diffusion distance for charge transfer provided by the ultrathin nanosheet structure, which inhibits the recombination of photogenerated charge carriers. This work not only opens up a possible pathway for the large-scale industrial preparation of BiOX (X = Cl, Br, I) with superior photocatalytic activity, but also provides new insight into environmental restoration and energy conversion.
首次在室温下通过离子液体诱导的机械化学合成方法,使用1-十六烷基-3-甲基咪唑溴盐([Cmim]Br)制备了超薄BiOBr纳米片。透射电子显微镜和原子力显微镜图像显示,超薄BiOBr纳米片的平均直径约为200-300 nm,厚度为3-4 nm。作为对比,选择KBr作为制备BiOBr纳米片的溴源,实验结果表明离子液体和机械球磨法对纳米片结构的制备有显著影响。与制备的对照样品相比,超薄BiOBr纳米片光催化剂对有机污染物的去除表现出显著提高的光催化性能。基于超薄纳米片结构提供的电荷转移扩散距离较短,抑制了光生电荷载流子的复合,提出了这种增强活性的可能机制。这项工作不仅为大规模工业制备具有优异光催化活性的BiOX(X = Cl、Br、I)开辟了一条可能的途径,也为环境修复和能量转换提供了新的见解。