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TiO_2@Perylene Diimide Full-Spectrum Photocatalysts via Semi-Core-Shell Structure

机译:TiO_2 @ Perylene二酰亚胺全光谱光催化剂通过半核 - 壳结构

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摘要

A semi-core-shell structure of perylene diimide (PDI) self-assembly coated with TiO_2 nanoparticles is constructed, in which nanoscale porous TiO_2 shell is formed and PDI self-assembly presented 1D structure. A full-spectrum photocatalyst is obtained using this structure to resolve a conundrum-TiO_2 does not exhibit visible-light photocatalytic activity while PDI does not exhibit ultraviolet photocatalytic activity. Furthermore, the synergistic interaction between TiO_2 and PDI enables the catalyst to improve its ultraviolet, visible-light, and full-spectrum performance. The interaction between TiO_2 and PDI leads to formation of some new stacking states along the Π-Π stacking direction and, as a consequence, electron transfer from PDI to TiO_2 suppresses the recombination of e~-/h~+ and thus improves photocatalytic performance. But the stronger interaction in the interface between TiO_2 and PDI is not in favor of photocatalytic performance, which leads to rapid charge recombination due to more disordered stacking states. The study provides a theoretical direction for the study of core-shell structures with soft materials as a core, and an idea for efficient utilization of solar energy.
机译:构造了涂有TiO_2纳米颗粒的Per丙二酰二酰亚胺(PDI)自组装的半核 - 壳结构,其中形成纳米级多孔TiO_2壳,并且PDI自组装呈现1D结构。使用该结构获得全光谱光催化剂以解析Conundrum-TiO_2,不表现出可见光的光催化活性,而PDI不表现出紫外光催化活性。此外,TiO_2和PDI之间的协同相互作用使催化剂能够改善其紫外,可见光和全光谱性能。 TiO_2和PDI之间的相互作用导致沿π-π堆叠方向形成一些新的堆叠状态,结果,从PDI到TiO_2的电子转移抑制了E〜/ H〜+的重组,从而提高了光催化性能。但TiO_2和PDI之间的界面中的更强的相互作用并不赞有光催化性能,这导致由于更紊乱的堆叠状态而导致快速充电重组。该研究提供了一种理论方向,用于研究具有软材料作为核心的核壳结构,以及有效利用太阳能的思想。

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