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Band-gap engineering of layered covalent organic frameworks via controllable exfoliation for enhanced visible-light-driven hydrogen evolution

机译:通过可控制的剥落,对层状共价有机骨架进行带隙工程,以增强可见光驱动的氢气释放

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Covalent organic frameworks (COFs) has become known as a promising organic photo catalyst for hydrogen evolution reaction (HER) because of its highly designable structure at the molecular level and other advantages related to the photocatalytic reaction. Here, we report a facile approach to prepare few-layer COFs nanosheets from a typical layered COF (covalent triazine frameworks, CTFs) via intercalation and exfoliation with H2SO4 and (NH4)(2)S2O8. Both the experiments and DFT calculations revealed the exfoliated CTFs nanosheets owned tunable optical and electronic properties because of the introduced defect states. It can not only narrow the bandgap for improved visible light absorption, but also suppress the radiative electron-hole recombination. Besides, the ultrathin structure can shorten the diffusion length of the photoexcited electrons and provide more active sites. As a result, the exfoliated nanosheets (especially the FL-CTF-2 with an apparent quantum yield of 11.14%) show much-improved performance in visible-light-driven HER compared with bulk CTFs. This work provides a new route to tail the photoelectric properties of COFs and may promote their applications in solar energy capture and conversion. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:共价有机骨架(COF)由于在分子水平上具有高度可设计的结构以及与光催化反应有关的其他优点,因此已成为有前途的氢释放反应有机光催化剂(HER)。在这里,我们报告了一种简便的方法,可以通过典型的分层COF(共价三嗪骨架,CTF)通过嵌入和剥离H2SO4和(NH4)(2)S2O8来制备几层COFs纳米片。实验和DFT计算都表明,由于引入的缺陷状态,剥离的CTFs纳米片具有可调的光学和电子性质。它不仅可以缩小带隙以改善可见光吸收,而且可以抑制辐射电子-空穴复合。此外,超薄结构可以缩短光激发电子的扩散长度,并提供更多的活性位点。结果,与大量CTF相比,剥离的纳米片(尤其是表观量子产率为11.14%的FL-CTF-2)在可见光驱动的HER中表现出大大改善的性能。这项工作为尾随COF的光电特性提供了一条新途径,并可能促进它们在太阳能捕获和转化中的应用。 (C)2019氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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