2D/2D Nb3O7F/g-C3N4 Heterojunction Photocatalysts with Enhanced Hydrogen Evolution Activity
Source abstract
Abstract
Constructing two-dimensional (2D)/2D heterojunctions with intimate interfacial contact is of great importance to achieve high photocatalytic efficiency for hydrogen evolution. Herein, 2D/2D niobium oxyfluoride (Nb3O7F)/graphitic carbon nitride (g-C3N4) heterojunction photocatalysts were prepared by a two-step hydrothermal/calcination method. As expected, the obtained 2D/2D Nb3O7F/g-C3N4 heterojunctions exhibited a high photocatalytic hydrogen evolution rate of 1242.0 μmol h–1 g–1, which was approximately 3 times higher than that of pure g-C3N4 (427.2 μmol h–1 g–1). Furthermore, cycling experiments verified that the heterojunctions have good stability after four cycles. The remarkable photocatalytic activity was predominantly attributed to the enhanced specific surface area, the improved photogenerated electron/hole separation efficiency, and the inhibited carrier recombination. This work may give a deep insight into heterojunction photocatalysts for application of hydrogen production.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Gas Sensing Nanomaterials and Sensors · 2D Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Low Carbon Energy Institute, China University of Mining and Technology, Xuzhou 221008, China
School of Materials Science and Physics, China University of Mining and Technology, Xuzhou 221116, China
Jiangsu Key Laboratory of Coal-Based Greenhouse Gas Control and Utilization, China University of Mining and Technology, Xuzhou 221008, China
Funding
Ministry of Education of the People's Republic of China
References (35)
Show source-provided references
1. 10.1038/natrevmats.2017.5010.1038/natrevmats.2017.50 ↗
2. 10.1016/j.mattod.2018.04.00810.1016/j.mattod.2018.04.008 ↗
3. 10.1002/advs.20180082010.1002/advs.201800820 ↗
4. 10.1039/c8se00507a10.1039/c8se00507a ↗
5. 10.1016/j.cej.2019.12371010.1016/j.cej.2019.123710 ↗
6. 10.1016/j.carbon.2017.06.02010.1016/j.carbon.2017.06.020 ↗
7. 10.1039/c9se00173e10.1039/c9se00173e ↗
8. 10.1021/acsaem.8b0095610.1021/acsaem.8b00956 ↗
9. 10.1016/j.apcatb.2019.11777910.1016/j.apcatb.2019.117779 ↗
10. 10.1002/aenm.20170150310.1002/aenm.201701503 ↗
11. 10.1021/jacs.9b0687210.1021/jacs.9b06872 ↗
12. 10.1016/j.apcatb.2019.11824910.1016/j.apcatb.2019.118249 ↗
13. 10.1002/aenm.20170002510.1002/aenm.201700025 ↗
14. 10.1016/j.cclet.2019.07.02110.1016/j.cclet.2019.07.021 ↗
15. 10.1016/j.nanoen.2016.06.03710.1016/j.nanoen.2016.06.037 ↗
16. 10.1039/c5nr07695a10.1039/c5nr07695a ↗
17. 10.1021/jacs.7b0841610.1021/jacs.7b08416 ↗
18. 10.1002/adfm.20190248610.1002/adfm.201902486 ↗
19. 10.3891/acta.chem.scand.18-233910.3891/acta.chem.scand.18-2339 ↗
20. 10.1007/s12034-019-1828-y10.1007/s12034-019-1828-y ↗
21. 10.1039/c3ce41210e10.1039/c3ce41210e ↗
22. 10.1038/srep3997310.1038/srep39973 ↗
23. 10.1088/1361-6528/ab704110.1088/1361-6528/ab7041 ↗
24. 10.1002/anie.20140337510.1002/anie.201403375 ↗
25. 10.1016/j.apcatb.2019.05.03210.1016/j.apcatb.2019.05.032 ↗
26. 10.1016/j.carbon.2019.09.08310.1016/j.carbon.2019.09.083 ↗
27. 10.1021/acsami.0c0515810.1021/acsami.0c05158 ↗
28. 10.1088/1361-6528/aab68e10.1088/1361-6528/aab68e ↗
29. 10.1016/j.matlet.2017.11.12410.1016/j.matlet.2017.11.124 ↗
30. 10.1021/cm101910210.1021/cm1019102 ↗
31. 10.1021/acscatal.6b0333410.1021/acscatal.6b03334 ↗
32. 10.1002/adma.20190636110.1002/adma.201906361 ↗
33. 10.1038/nenergy.2017.3110.1038/nenergy.2017.31 ↗
34. 10.1021/acscatal.7b0343710.1021/acscatal.7b03437 ↗
35. 10.1016/j.apcatb.2020.11925410.1016/j.apcatb.2020.119254 ↗