Embedding 1D WO3 Nanotubes into 2D Ultrathin Porous g-C3N4 to Improve the Stability and Efficiency of Photocatalytic Hydrogen Production

光催化 材料科学 制氢 化学工程 催化作用 兴奋剂 多孔性 纳米技术 可见光谱 纳米管 碳纳米管 光电子学 化学 复合材料 有机化学 工程类
作者
Feng Fang,Hongfeng Hua,Lutao Li,Rongxi Xu,Jiayu Tang,Dejiang Dong,Jian Zhang,Xing’ao Li
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:4 (5): 4365-4375 被引量:37
标识
DOI:10.1021/acsaem.0c03168
摘要

Recently, two-dimensional (2D) g-C3N4 has attracted great interest for visible-light-driven H2 production. Thinning, doping, and reticulation have been demonstrated as effective strategies to improve the efficiency of photocatalysis, but are a challenge for structural stability. Herein, a targeted method was implemented by embedding the one-dimensional (1D) WO3 nanotubes matrix into the frameworks of 2D porous g-C3N4 to form a porous P-doped g-C3N4 nanosheets/WO3 nanotubes (PCNS/WNT) by a flexible electrostatic self-assembly process. As a visible-light-sensitive photocatalyst, the as-prepared hybrids exhibited impressive performance for hydrogen generation, which was attributed to the advantages of synergetic mechanism owing to a higher specific surface area, more reaction active sites, enhanced light absorption, and a better photogenerated carrier separation. Interestingly, the insertion of 1D WO3 nanotubes not only accelerates electrons transfer along the 1D channel but also provides robust support for 2D porous g-C3N4 architecture. As a result, the maximum photocatalytic H2 evolution rate of PCNW-50 is 547 μmol g–1 h–1, which is about four times higher than that of pure PCNS, and there is no significant reduction of H2 production after five cycles. Moreover, this 2D/1D PCNS/WNT hybrid was first reported in the area of photocatalytic hydrogen evolution and provides ideas for designing novel stable architecture of photocatalyst.
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