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0D, 1D, 2D molybdenum disulfide functionalized by 2D polymeric carbon nitride for photocatalytic water splitting

机译:0D、1D、2D二硫化钼通过2D聚合氮化碳功能化用于光催化分解水

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摘要

Photocatalytic activity of molybdenum disulfide structures with different dimensions (0D, 1D and 2D) functionalized with polymeric carbon nitride (PCN) is presented. MoS2 nanotubes (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 MoS2 arose 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.
机译:介绍了用聚合氮化碳(PCN)功能化的不同尺寸(0D、1D和2D)二硫化钼结构的光催化活性。分别以MoS2纳米管(1D)、纳米片(2D)和量子点(0D、QDs)为PCN的助催化剂,在光催化分解水反应中放出氢气。虽然2D-PCN在460-727 nm的光照射下显示出最高的可见光吸收率和最增强的光电流响应,但QDs-PCN显示出最高的光催化效率。详细分析表明,与MoS2的其他结构相比,QDs-PCN具有优越的光催化活性,这源于(i)最有效的光激发电子-空穴对分离,(ii)最增强的上转换光致发光(UCPL),(iii)电子在导带中的反应性最高。此外,QDs的尺寸变窄影响了电荷载流子向活性反应位点的扩散路径较短,位点数量较多,二硫化钼与PCN之间的界面面积较大。

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