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用于高效光催化析氢的一维石墨相氮化碳链纳米结构的无模板合成

Template-Free Synthesis of One-Dimensional g-CN Chain Nanostructures for Efficient Photocatalytic Hydrogen Evolution.

作者信息

Zhang Mingyi, Sun Ye, Chang Xin, Zhang Peng

机构信息

Key Laboratory for Photonic and Electronic Bandgap Materials, Ministry of Education, School of Physics and Electronic Engineering, Harbin Normal University, Harbin, China.

School of Materials Science and Engineering, Zhengzhou University, Zhengzhou, China.

出版信息

Front Chem. 2021 Mar 15;9:652762. doi: 10.3389/fchem.2021.652762. eCollection 2021.

Abstract

The development of graphite-carbon nitride (g-CN) photocatalyst is of great significance for various visible utilization applications. Control the nanostructures of g-CN can tailor its photocatalytic performance. In this paper, one-dimensional chain-like g-CN was successfully synthesized by heat-induced polymerization of melamine which was saturated in ethylene glycol. The photocatalytic hydrogen production rate (HER) of the prepared g-CN chain enhanced about 3 times than that of bulk g-CN, increasing from 9.6 μmolh to 28.7 μmolh. The improved photocatalytic activity of the g-CN chain was attributed to the advantages of porosity and nanostructure. The extraordinary nanopores result in an enlarged specific surface area for adsorption and the production of abundantly available channels for charge transfer. The one-dimensional chain-like structure can facilitate the exposure of internal/external active sites as many as possible, and induce the directional migration of charge carriers.

摘要

石墨相氮化碳(g-CN)光催化剂的开发对于各种可见光利用应用具有重要意义。控制g-CN的纳米结构可以调整其光催化性能。本文通过对在乙二醇中饱和的三聚氰胺进行热诱导聚合,成功合成了一维链状g-CN。制备的g-CN链的光催化产氢速率(HER)比块状g-CN提高了约3倍,从9.6 μmol/h增加到28.7 μmol/h。g-CN链光催化活性的提高归因于孔隙率和纳米结构的优势。特殊的纳米孔导致吸附的比表面积增大,并产生大量用于电荷转移的可用通道。一维链状结构可以促进尽可能多的内部/外部活性位点的暴露,并诱导电荷载流子的定向迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4b6/8005558/e19175b243b2/fchem-09-652762-g001.jpg

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