Phase Transformation Synthesis of Strontium Tantalum Oxynitride-Based Heterojunction for Improved Visible Light-Driven Hydrogen Evolution
Source abstract
Abstract
Tantalum oxynitride-based materials, which possess narrow band gaps and sufficient band energy potentials, have been of immense interest for water splitting. However, the efficiency of photocatalytic reactions is still low because of the fast electron–hole recombination. Here, a Sr 2 Ta 2 O 7– x N x /SrTaO 2 N heterostructured photocatalyst with a well-matched band structure was in situ constructed by the nitridation of hydrothermal-prepared Sr 2 Ta 2 O 7 nanosheets. Compared to Sr 2 Ta 2 O 7– x N x and pure SrTaO 2 N, the Sr 2 Ta 2 O 7– x N x /SrTaO 2 N heterostructured photocatalyst exhibited the highest rate of hydrogen evolution, which is ca. 2.0 and 76.4 times of Sr 2 Ta 2 O 7– x N x and pure SrTaO 2 N, respectively, under the similar reaction condition. The enhanced performance arises from the formation of suitable band-matched heterojunction-accelerated charge separation. This work provides a promising strategy for the construction of tantalum oxynitride-based heterojunction photocatalysts.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · MXene and MAX Phase Materials · Machine Learning in Materials Science
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Skate Key Laboratory for Powder Metallurgy, Central South University, Changsha 410083, P. R. China
Department of Chemical and Biomolecular Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260, Singapore
Funding
National Natural Science Foundation of China · Science Fund for Distinguished Young Scholars of Hunan Province
References (38)
Show source-provided references
1. 10.1038/414625a10.1038/414625a ↗
2. 10.1039/c3cs60378d10.1039/c3cs60378d ↗
3. 10.1039/c6cc03739a10.1039/c6cc03739a ↗
4. 10.1016/j.scib.2017.03.00510.1016/j.scib.2017.03.005 ↗
5. 10.1002/adma.20160514810.1002/adma.201605148 ↗
6. 10.1002/adfm.20050084910.1002/adfm.200500849 ↗
7. 10.1039/c1ee01259b10.1039/c1ee01259b ↗
8. 10.1021/nn102469e10.1021/nn102469e ↗
9. 10.1021/am403025q10.1021/am403025q ↗
10. 10.1021/jp991905610.1021/jp9919056 ↗
11. 10.1021/cm010903710.1021/cm0109037 ↗
12. 10.1021/ja027751g10.1021/ja027751g ↗
13. 10.1021/jp202783t10.1021/jp202783t ↗
14. 10.1021/ja304367810.1021/ja3043678 ↗
15. 10.1039/c4cc06682k10.1039/c4cc06682k ↗
16. 10.1021/acsami.6b1423010.1021/acsami.6b14230 ↗
17. 10.1016/j.apcatb.2018.01.07110.1016/j.apcatb.2018.01.071 ↗
18. 10.1039/c5ta07057k10.1039/c5ta07057k ↗
19. 10.1039/c0cy00029a10.1039/c0cy00029a ↗
20. 10.1002/adfm.20100059110.1002/adfm.201000591 ↗
21. 10.1039/c3nr34096a10.1039/c3nr34096a ↗
22. 10.1039/c4ce01774a10.1039/c4ce01774a ↗
23. 10.1002/ange.20170864510.1002/ange.201708645 ↗
24. 10.1039/c3ta10446j10.1039/c3ta10446j ↗
25. 10.1039/b800489g10.1039/b800489g ↗
26. 10.1039/c2cs35355e10.1039/c2cs35355e ↗
27. 10.1002/adma.20160169410.1002/adma.201601694 ↗
28. 10.1002/anie.20150268610.1002/anie.201502686 ↗
29. 10.1016/j.apcatb.2015.11.04110.1016/j.apcatb.2015.11.041 ↗
30. 10.1016/j.apcatb.2017.05.09210.1016/j.apcatb.2017.05.092 ↗
31. 10.1039/c6sc02750d10.1039/c6sc02750d ↗
32. 10.1002/aenm.20170017110.1002/aenm.201700171 ↗
33. 10.1002/1521-3757(20020802)114:15<2935::aid-ange2935>3.0.co;2-610.1002/1521-3757(20020802)114:15<2935::aid-ange2935>3.0.co;2-6 ↗
34. 10.1038/nmat369710.1038/nmat3697 ↗
35. 10.1016/j.apcatb.2017.06.03310.1016/j.apcatb.2017.06.033 ↗
36. 10.1016/j.apcatb.2017.09.00210.1016/j.apcatb.2017.09.002 ↗
37. 10.1016/j.ijhydene.2008.12.07410.1016/j.ijhydene.2008.12.074 ↗
38. 10.1039/c4ee02914c10.1039/c4ee02914c ↗