4.7 Article

In situ one-step hydrothermal synthesis of oxygen-containing groups-modified g-C3N4 for the improved photocatalytic H2-evolution performance

期刊

APPLIED SURFACE SCIENCE
卷 427, 期 -, 页码 645-653

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2017.08.050

关键词

g-C3N4; Modification; Hydrothermal treatment; Oxygen functionalities; Increased surface area; Hydrogen evolution photocatalyst

资金

  1. National Natural Science Foundation of China [51472192, 21477094, 51672203]
  2. Fundamental Research Funds for the Central Universities [WUT 2017IB002]

向作者/读者索取更多资源

Surface modification of g-C3N4 is one of the most effective strategies to boost its photocatalytic H-2-evolution performance via promoting the interfacial catalytic reactions. In this study, an in situ one-step hydrothermal method was developed to prepare the oxygen-containing groups-modified g-C3N4 (OG/gC(3)N(4)) by a facile and green hydrothermal treatment of bulk g-C3N4 in pure water without any additives. It was found that the hydrothermal treatment (180 degrees C) not only could greatly increase the specific surface area (from 2.3 to 69.8 m(2) g(-1)), but also caused the formation of oxygen-containing groups (-OH and C=O) on the OG/g-C3N4 surface, via the interlayer delamination and intralayer depolymerization of bulk g-C3N4. Photocatalytic experimental results indicated that after hydrothermal treatment, the resultant OG/g-C3N4 samples showed an obviously improved H-2-evolution performance. Especially, when the hydrothermal time was 6 h, the resultant OG/g-C3N4(6 h) exhibited the highest photocatalytic activity, which was clearly higher than that of the bulk g-C3N4 by a factor of ca. 7. In addition to the higher specific surface area, the enhanced H-2-evolution rate of OG/g-C3N4 photocatalysts can be mainly attributed to the formation of oxygen-containing groups, which possibly works as the effective H-2-evolution active sites. Considering the facie and green synthesis method, the present work may provide a new insight for the development of highly efficient photocatalytic materials. (C) 2017 Elsevier B.V. All rights reserved.

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