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由超薄自掺杂纳米片组装而成的三维分级石墨相氮化碳结构:极其简便的六亚甲基四胺活化法及优异的光催化析氢性能

Three-Dimensional Hierarchical g-CN Architectures Assembled by Ultrathin Self-Doped Nanosheets: Extremely Facile Hexamethylenetetramine Activation and Superior Photocatalytic Hydrogen Evolution.

作者信息

Gao Huihui, Cao Ruya, Zhang Shouwei, Yang Hongcen, Xu Xijin

机构信息

School of Physics and Technology , University of Jinan , Jinan , Shandong 250022 , P. R. China.

出版信息

ACS Appl Mater Interfaces. 2019 Jan 16;11(2):2050-2059. doi: 10.1021/acsami.8b17757. Epub 2019 Jan 2.

Abstract

Photocatalytic hydrogen evolution has broad prospects as a clean solution for the energy crisis. However, the rational design of catalyst complex, the H evolution efficiency, and the yield are great challenge. Herein, three-dimensional hierarchical g-CN architectures assembled by ultrathin carbon-rich nanosheets (3D CCNS) were prepared via an extremely facile hexamethylenetetramine activation approach at the bulk scale, indicating the validation of scale-up production process. The two-dimensional ultrathin carbon-rich nanosheets were several hundred nanometers in width but only 5-6 nm in thickness and gave rise to a unique 3D interconnected network. The unique composition and structure of the nanosheets endow them with a remarkable light absorption spectrum with the tunable band gap, high electrical conductivity, fast charge separation, and large surface areas with abundant reaction active sites, and thus significantly improved H production performance. As high as ∼7.8%, quantum efficiency can be achieved by irradiating 3D CCNS at 420 nm with a H evolution rate >2.7 × 10 μmol/g/h, which is ∼31.3 times higher than that of the pristine g-CN. Our work introduces an extremely facile route for mass production of doping modified 3D g-CN-based photocatalyst with excellent H evolution performances.

摘要

光催化析氢作为解决能源危机的一种清洁方案具有广阔前景。然而,催化剂复合物的合理设计、析氢效率和产率是巨大挑战。在此,通过一种极其简便的六亚甲基四胺活化方法在大规模制备了由超薄富碳纳米片组装而成的三维分级g-CN结构(3D CCNS),这表明放大生产过程的有效性。二维超薄富碳纳米片宽度达几百纳米,但厚度仅为5 - 6纳米,并形成了独特的三维互连网络。纳米片独特的组成和结构赋予它们具有可调带隙的显著光吸收光谱、高电导率、快速电荷分离以及具有丰富反应活性位点的大表面积,从而显著提高了产氢性能。通过在420纳米处照射3D CCNS,析氢速率>2.7×10 μmol/g/h,可实现高达约7.8%的量子效率,这比原始g-CN高出约31.3倍。我们的工作为大规模生产具有优异析氢性能的掺杂改性3D g-CN基光催化剂引入了一条极其简便的途径。

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