摘要
The photocatalytic water splitting capability of metal-free graphitic carbon nitride (g-C3N4) photocatalyst is determined by its microstructure and photoexcited electrons transfer. Herein, a segmented structure was developed, consisting of alternant g-C3N4 nanotubes and graphitic carbon rings (denoted as Cr-CN-NT). The Cr-CN-NT showed ordered structure and ultralong length/diameter ratio of 150 nm in diameter and a few microns in lengths, which promoted electron transport kinetics and elongated photocarrier diffusion length and lifetime. Meanwhile, the local in-plane π-conjugation was formed and extended in Cr-CN-NT, which could improve charge carrier density and prohibit electron–hole recombination. Accordingly, the average hydrogen evolution rate of Cr-CN-NT reached 9245 μmol h−1 g−1, which was 61.6 times that of pristine CN, and the remarkable apparent quantum efficiency (AQE) of Cr-CN-NT reached up to 12.86 % at 420 nm. This work may provide a pathway for simultaneous morphology regulation and in-plane modification of high-performance photocatalysts.
| 源语言 | 英语 |
|---|---|
| 文章编号 | e202201268 |
| 期刊 | ChemSusChem |
| 卷 | 15 |
| 期 | 20 |
| DOI | |
| 出版状态 | 已出版 - 21 10月 2022 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 7 经济适用的清洁能源
学术指纹
探究 'Segmented Structure Design of Carbon Ring In-Plane Embedded in g-C3N4 Nanotubes for Ultra-High Hydrogen Production' 的科研主题。它们共同构成独一无二的学术指纹。引用此
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