Giant enhanced photocatalytic H2O2 production over hollow hexagonal prisms carbon nitride

光催化 光电流 材料科学 X射线光电子能谱 高分辨率透射电子显微镜 量子效率 化学工程 纳米技术 氮化碳 电子空穴 六方晶系 打赌理论 石墨氮化碳 催化作用 电子 透射电子显微镜 光电子学 化学 物理 结晶学 工程类 量子力学 生物化学
作者
Teng Ge,Xiaoli Jin,Jianliang Cao,Zhuohua Chen,Yixue Xu,Haiquan Xie,Fengyun Su,Xin Li,Qing Lan,Liqun Ye
出处
期刊:Journal of The Taiwan Institute of Chemical Engineers [Elsevier BV]
卷期号:129: 104-111 被引量:25
标识
DOI:10.1016/j.jtice.2021.09.036
摘要

H2O2, as a green and environmentally friendly oxidant, has been widely used in our daily life and industrial production. It is of epoch-making significance to develop highly efficient photocatalysts for producing H2O2. In recent years, g-C3N4 has received much attention due to its high chemical stability, environmental friendliness and suitable energy band structure. However, some shortcomings including the fast recombination of photogenerated electron-hole pairs and small specific surface area in traditional 2D g-C3N4 seriously impede its photocatalytic performance for the production of H2O2. 1D hollow nanostructures possess intriguing physicochemical properties and are adopted to overcome the intrinsic shortcomings of g-C3N4. Herein, g-C3N4 with a hollow hexagonal prism structure (CNHP) is prepared to produce H2O2. It is characterized by XRD, XPS, SEM, HRTEM, ESR and DRS. BET, PL spectra, photocurrent and EIS are used to explain the enhanced photocatalytic performance. Compared with traditional 2D g-C3N4, the specific surface area of CNHP increases to 41.513 m2/g, providing more active sites. Meanwhile, its hollow tubular structure can enhance the migration of photogenerated electrons to the catalyst surface, and electrons with a longer lifetime can participate in photocatalytic reactions to achieve high efficiency. The yield of H2O2 production can up to 4.08 μmol over CNHP in 40 min, which is about 7 times higher than that of traditional 2D g-C3N4, and the apparent quantum efficiency (AQE) of H2O2 production at 420 nm is 2.41%. This research provides a valuable reference for the development of green materials for efficient photocatalytic production of H2O2.
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