光催化
石墨氮化碳
剥脱关节
纳米结构
材料科学
分解水
化学工程
氮化碳
石墨
冷凝
兴奋剂
纳米技术
化学
光电子学
催化作用
复合材料
工程类
有机化学
石墨烯
物理
热力学
作者
Hamza Majeed Ansari,Weijia Wang,Lin Lei,Kuo Bao,Xinye Chang,Ali Raza,Yongfeng Chen,Asad Mehboob,Qi Zhong,Anurag Srivastava,О. С. Каймиева,Huiqing Fan
标识
DOI:10.1016/j.jallcom.2022.165794
摘要
Graphitic carbon nitride (g-C3N4) shows a graphite-like layered structure, which provides a high theoretical value for solar-to-hydrogen evolution especially for a 2D nanostructure. However, conventional polycondensation induces a strong agglomeration and collapse of nanostructure, resulting in a relatively poor photocatalytic performance. To overcome this problem, we develop a gas bubbling exfoliation strategy with NH4Cl assistant to make ultrathin 2D g-C3N4 nanosheets self-assembled into a 3D macroporous network on a large scale. The hierarchical structure significantly improves the specific surface area to 176.4 m2 g−1 (11.6 times higher than the reference g-C3N4), which allows a large water/g-C3N4 interface for photocatalytic water reduction reaction. The ultrathin 2D g-C3N4 nanosheets show a thickness of about 1.4 nm, which greatly suppress photoinduced carriers recombination and enhance charge transfer at the interface. Furthermore, the doping of N and Cl is achieved during synthesis. As a result, the resulting g-C3N4 demonstrates a remarkable improvement in H2 production of 12.89 mmol g-1 h−1, which is 21 times higher than the g-C3N4 obtained from the conventional condensation method. These explorations provide a facile guidance for the quasi 3D g-C3N4 hierarchical architecture engineering even for various energy-related applications.
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