4.7 Article

A facile synthesis of nano-layer structured g-C3N4 with efficient organic degradation and hydrogen evolution using a MDN energetic material as the starting precursor

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 44, 期 8, 页码 4102-4113

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2018.12.171

关键词

g-C3N4; Photocatalyst; Nano-layers; Melaminium dinitrate; H-2 production; RhB degradation

资金

  1. National Natural Science Foundation of China for Youth [21207093]
  2. Natural Science Foundation of Shenyang Science and Technology Bureau, Liaoning Province, China [18-013-0-02]
  3. Liaoning Province Excellent Talents in University, China [LJQ2014023]

向作者/读者索取更多资源

The construction of a high-performance g-C3N4 photocatalyst through a facile and green synthesis method remains a great challenge for H-2 production and organic pollutants degradation. In this work, we developed a nano-layer structured g-C3N4 (NL-CN) photo-catalyst with a 230 m(2)/g surface area via the thermal polymerization method using melaminium dinitrate (MDN), which is one of the more energetic materials, as the precursor. The energy coming from the drastic decomposition of nitrate anions in MDN caused the thick layers of bulk CN to be exfoliated to produce many much-thinner nano-layers when at 500 degrees C for 2 h, which obviously elevated the surface area of the g-C3N4. The resultant NL-CN displays a superior visible-light H-2-generation and rhodamine B (RhB) photo-degradation efficiency (lambda > 420 nm) compared to those of bulk g-C3N4 (CN) prepared through heating melamine because of the nano-layered structures, which lead to higher specific surface areas, a rapid charge transfer efficiency and a higher redox potential. These results demonstrate that the utilization of MDN as a starting material provides a new opportunity for the facile and green synthesis of high-efficiency nanostructured g-C3N4 photocatalysts with lower energy consumption and environmental pollution levels. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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