四氢呋喃
剥脱关节
石墨氮化碳
催化作用
材料科学
溶剂
石墨烯
氮化碳
单层
化学工程
纳米技术
化学
光化学
有机化学
光催化
工程类
作者
Thanh Truong Dang,Thi Kim Anh Nguyen,K.C. Bhamu,Tahereh Mahvelati-Shamsabadi,Vo Kim Hieu Van,Eun Woo Shin,Koo–Hyun Chung,Seung Hyun Hur,Won Mook Choi,Sung Gu Kang,Jin Suk Chung
出处
期刊:ACS Catalysis
日期:2022-10-26
卷期号:12 (21): 13763-13780
被引量:33
标识
DOI:10.1021/acscatal.2c03523
摘要
In this work, we present the in situ exfoliation of graphitic carbon nitride (g-C3N4), engineering holey defects on 2D g-C3N4 layers, and formation of self-assembled graphene via solvothermal treatment of g-C3N4-bulk in various organic solvents. Methyl alcohol, isopropyl alcohol, tetrahydrofuran, and dimethylformamide were chosen for exfoliating and modifying g-C3N4 sheets based on their compatibility with g-C3N4 in Hansen parameters. Uniform holey defects on 2D g-C3N4 nanosheets were successfully engineered using tetrahydrofuran solvent in a facile solvothermal process. The introduction of N vacancies in heptazine units and the formation of the holey structure of tetrahydrofuran-modified g-C3N4 sample (C3N4-THF) led to high photocatalytic performance due to enhanced mass transfer, shortening of the charge diffusion lengths, and increased charge separation during the photocatalysis process. Furthermore, full exfoliation of the engineered nanostructure of holey defect C3N4-THF into a monolayer in reaction media led to maximizing accessible reducing and oxidizing active sites. As a result, the C3N4-THF sample achieved photocatalytic activity with a H2 evolution rate at stationary point as high as 31256.9 μmol h–1 g–1 under 1 Sun illumination of a solar simulator.
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