材料科学
三聚氰胺
光催化
氮化碳
碳纤维
热液循环
纳米技术
化学工程
氮化物
催化作用
氢
石墨
化学
复合材料
有机化学
复合数
工程类
图层(电子)
作者
Yun Yang,Jinzhe Liu,Chencheng Zhou,Peilin Zhang,Shouzhi Guo,Shuo Li,Xingjun Meng,Yue Lu,Huajiang Xu,Haojie Ma,Luyang Chen
标识
DOI:10.1016/j.ijhydene.2019.08.172
摘要
Abstract Novel carbon self-doped graphitic carbon nitride tube (denoted as C-CNT) was fabricated by the means of a facile in situ solvothermal method with melamine and glucose as precursor and additive, respectively. The C-CNT not only remained unique hexagonal tubular structure obtained from supramolecular self-assembly method, but also introduced aromatic carbon into CN framework under the glucose-assisted hydrothermal conditions. The as-prepared C-CNT exposed abundant nitrogen defects and dramatically improved the valid separation of photoexcited charge carriers, hence achieving excellent photocatalytic hydrogen evolution activity (32.3 μmol h−1, λ > 420 nm), which was up to 4.24 and 12-folds higher than pristine carbon nitride tube (CNT) and traditional bulk counterpart (BCN), respectively. Therefore, this work highlights an assisted hydrothermal approach to successfully prepare carbon-rich graphitic carbon nitride with hexagonal tubular structure.
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