Chemical & Material Sciences Division, CSIR-Indian Institute of Petroleum, Dehradun, 248005 India; Academy of Scientific and Innovative Research (AcSIR), New Delhi, 110001, India.
Department of Pure and Applied Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305-8573, Japan.
J Hazard Mater. 2020 Apr 5;387:121700. doi: 10.1016/j.jhazmat.2019.121700. Epub 2019 Nov 18.
In this report, a ternary Ag-rGO/g-CN hybrid was synthesized by a simple hydrothermal approach for the photocatalytic reduction of nitroarene compounds into their corresponding amines under visible light. Importantly, the present method did not require reducing agents, like hydrazine hydrate; instead methanol has been used as a source of electrons and protons for the photoreduction process. After grafting of Ag NPs, a significant enhancement in the efficiency of the rGO/g-CN for the reduction of nitrobenzenes was observed. Under optimized experimental conditions, the conversion of nitrobenzene and yield of aniline were determined to be 99% and 98%, respectively under visible light illumination for 4 h. The nitrobenzene compounds bearing both electron donating and withdrawing groups were selectively converted into their corresponding aniline products without altering the functionality. The enhanced performance of the developed photocatalyst attributed to the effective separation of photoexcited electrons on the photocatalyst surface and their subsequent transfer for the reduction of nitrobenzene molecules.
在本报告中,通过一种简单的水热方法合成了三元 Ag-rGO/g-CN 杂化材料,用于在可见光下光催化还原硝基芳烃化合物成相应的胺。重要的是,本方法不需要还原剂,如肼;相反,甲醇被用作光还原过程中电子和质子的来源。在接枝 Ag NPs 后,rGO/g-CN 对硝基苯的还原效率显著提高。在优化的实验条件下,在可见光照射 4 小时下,硝基苯的转化率和苯胺的产率分别为 99%和 98%。带有供电子和吸电子基团的硝基苯化合物被选择性地转化为相应的苯胺产物,而不改变其官能团。所开发的光催化剂的增强性能归因于光催化剂表面上光激发电子的有效分离及其随后转移用于还原硝基苯分子。