pH dependent morphology and texture evolution of ZnO nanoparticles fabricated by microwave-assisted chemical synthesis and their photocatalytic dye degradation activities

被引:24
作者
Arellano-Cortaza, M. [1 ]
Ramirez-Morales, E. [1 ]
Pal, U. [2 ]
Perez-Hernandez, G. [1 ]
Rojas-Blanco, L. [1 ]
机构
[1] Univ Juarez Autonoma Tabasco, Ave Univ S-N, Villahermosa Centro 86690, Tabasco, Mexico
[2] Benemerita Univ Autanoma Puebla, Inst Fis, Apartado Postal J-48, Puebla 72570, Pue, Mexico
关键词
Microwave assisted synthesis; pH control; ZnO nanoparticles; Photocatalysis; VISIBLE-LIGHT; SURFACE-AREA; SOL-GEL; PERFORMANCE; NANOSTRUCTURES; TEMPERATURE; HYBRID; IMPACT; TIO2;
D O I
10.1016/j.ceramint.2021.06.170
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
ZnO nanostructures are well-known photocatalysts for the degradation of toxic organic dyes and their morphology, size, and other physicochemical properties play important roles in their photocatalytic performance. To study the effect of size, morphology, and synthesis conditions in photocatalytic performance, we synthesized ZnO nanoparticles of different morphologies through a simple microwave-assisted chemical process at different pH values of the reaction mixture. Different pH values of the reaction mixture produced ZnO nanoparticles of different morphologies and sizes. The nature of the pH controlling agent and final pH of the reaction mixture were seen to have considerable effects on the lattice parameters and microstrain of the ZnO nanocrystals, along with their photocatalytic performance. We observed that while the ZnO nanostructures synthesized at very high pH values of the reaction mixture have a high specific surface area, their photocatalytic activity is higher when they are synthesized at acidic pH or pH near the isoelectric point of ZnO. The results demonstrate that the photocatalytic activity of ZnO nanostructures not only depends on their size or specific surface area but also strongly depends on the concentration of catalytic sites at their surface.
引用
收藏
页码:27469 / 27478
页数:10
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