Aleksandrzak Malgorzata, Baca Martyna, Pacia Michał, Wenelska Karolina, Zielinska Beata, Kalenczuk Ryszard J, Mijowska Ewa
Nanomaterials Physicochemistry Department, Faculty of Chemical Technology and Engineering, West Pomeranian University of Technology, Szczecin, Piastow Ave. 42, 71-065 Szczecin, Poland.
Faculty of Chemistry, Jagiellonian University in Kraków, Gronostajowa 2, 30-387 Kraków, Poland.
Nanotechnology. 2021 Jun 9;32(35). doi: 10.1088/1361-6528/ac04d3.
Photocatalytic activity of molybdenum disulfide structures with different dimensions (0D, 1D and 2D) functionalized with polymeric carbon nitride (PCN) is presented. MoSnanotubes (1D), nanoflakes (2D) and quantum dots (0D, QDs) were used, respectively, as co-catalysts of PCN in photocatalytic water splitting reaction to evolve hydrogen. Although, 2D-PCN showed the highest light absorption in visible range and the most enhanced photocurrent response after irradiation with light from 460 to 727 nm, QDs-PCN showed the highest photocatalytic efficiency. The detailed analysis revealed that the superior photocatalytic activity of QDs-PCN in comparison with other structures of MoSarose from (i) the most effective separation of photoexcited electron-hole pairs, (ii) the most enhanced up-converted photoluminescence (UCPL), (iii) the highest reactivity of electrons in conduction band. Moreover, a narrowed size of QDs affected shorter diffusion path of charge carriers to active reaction sites, higher number of the sites and higher interfacial area between molybdenum disulfide and PCN.
本文介绍了用聚合氮化碳(PCN)功能化的不同维度(0D、1D和2D)二硫化钼结构的光催化活性。分别使用二硫化钼纳米管(1D)、纳米片(2D)和量子点(0D,QDs)作为PCN在光催化水分解反应中产生氢气的共催化剂。尽管2D-PCN在可见光范围内显示出最高的光吸收,并且在用460至727nm的光照射后光电流响应增强最大,但QDs-PCN显示出最高的光催化效率。详细分析表明,与其他二硫化钼结构相比,QDs-PCN具有优异的光催化活性,这源于:(i)光激发电子-空穴对的最有效分离;(ii)上转换光致发光(UCPL)的最大增强;(iii)导带中电子的最高反应活性。此外,QDs尺寸的缩小影响了电荷载流子到活性反应位点的扩散路径更短、位点数量更多以及二硫化钼与PCN之间的界面面积更大。