Abinaya R, Archana J, Harish S, Navaneethan M, Ponnusamy S, Muthamizhchelvan C, Shimomura M, Hayakawa Y
Center for Material Science and Nanodevices, Department of Physics and Nanotechnology, SRM Institute of Science and Technology Kattankulathur-603 203 Tamil Nadu India
Graduate School of Science and Technology, Shizuoka University 3-5-1 Johoku, Naka-Ku Hamamatsu Shizuoka 432-8011 Japan.
RSC Adv. 2018 Jul 25;8(47):26664-26675. doi: 10.1039/c8ra02560f. eCollection 2018 Jul 24.
Edge-rich active sites of ultrathin layered molybdenum disulphide (MoS) nanosheets were synthesized by a hydrothermal method. The effect of pH on the formation of MoS nanosheets and their photocatalytic response have been investigated. Structural and elemental analysis confirm the presence of S-Mo-S in the composition. Morphological analysis confirms the presence of ultrathin layered nanosheets with a sheet thickness of 10-28 nm at pH 1. The interplanar spacing of MoS layers is in good agreement with the X-ray diffraction and high-resolution transmission electron microscopy results. A comparative study of the photocatalytic performance for the degradation of methylene blue (MB) and rhodamine B (RhB) by ultrathin layered MoS under visible light irradiation was performed. The photocatalytic activity of the edge-rich ultrathin layered nanosheets showed a fast response time of 36 min with the degradation rate of 95.3% of MB and 41.1% of RhB. The photocatalytic degradation of MB was superior to that of RhB because of the excellent adsorption of MB than that of RhB. Photogenerated superoxide radicals were the key active species for the decomposition of organic compounds present in water, as evidenced by scavenger studies.
通过水热法合成了具有丰富边缘活性位点的超薄层状二硫化钼(MoS)纳米片。研究了pH值对MoS纳米片形成及其光催化响应的影响。结构和元素分析证实了其组成中存在S-Mo-S。形态分析证实,在pH值为1时存在厚度为10-28nm的超薄层状纳米片。MoS层的面间距与X射线衍射和高分辨率透射电子显微镜结果吻合良好。对可见光照射下超薄层状MoS对亚甲基蓝(MB)和罗丹明B(RhB)降解的光催化性能进行了对比研究。富含边缘的超薄层状纳米片的光催化活性表现出快速响应时间36分钟,MB降解率为95.3%,RhB降解率为41.1%。由于MB比RhB具有更好的吸附性,MB的光催化降解优于RhB。清除剂研究表明,光生超氧自由基是水中有机化合物分解的关键活性物种。