Effect of carbon quantum dots on the photo‐absorption, photo‐response and photoelectrochemical performance of KNb 3 O 8 film photoelectrode
Source abstract
Abstract
Abstract The KNb 3 O 8 crystals and carbon quantum dots were synthesized via hydrothermal reaction method, their crystal structural and morphological properties were investigated by X‐ray diffraction, scanning electron microscope and transmission electron microscope, respectively. The X‐ray diffraction patterns of KNb 3 O 8 film on FTO glass (SnO 2 conductive glass doped with fluorine) show that the thin KNb 3 O 8 crystals are apt to stack along the [020] direction of KNb 3 O 8 crystal structure. Scanning electron microscope and transmission electron microscope results indicate that most of KNb 3 O 8 crystals have a width of about 0.5 μm and a length of more than 5 μm and the carbon quantum dot has a graphite structure with a size of about 3 nm. The UV‐response KNb 3 O 8 thin film electrode was loaded by carbon quantum dots and showed broader photo‐absorption characteristic (up to visible light region) and higher photocurrent (a bias of 0.4 V vs SCE), as compared of the pristine KNb 3 O 8 film electrode. In addition, their photo‐electrochemical (PEC) performances were also investigated under different light irradiation conditions with an applied potential between −0.4 and 0.7 V versus SCE.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Carbon and Quantum Dots Applications · Ga2O3 and related materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Information Science and Engineering Guilin University of Technology Guilin P. R. China
Key Laboratory of the Ministry of Education International Center for Dielectric Research Xi'an Jiaotong University Xi'an P. R. China
School of Materials Science and Engineering Guilin University of Technology Guilin P. R. China
References (29)
Show source-provided references
1. 10.1021/cr00033a00410.1021/cr00033a004 ↗
2. 10.1038/414625a10.1038/414625a ↗
3. 10.1039/C4MH00176A10.1039/C4MH00176A ↗
4. 10.1016/j.apcata.2005.04.03510.1016/j.apcata.2005.04.035 ↗
5. 10.1016/j.apcata.2005.08.01010.1016/j.apcata.2005.08.010 ↗
6. 10.1016/j.cattod.2015.09.02610.1016/j.cattod.2015.09.026 ↗
7. 10.1016/j.cattod.2015.11.02910.1016/j.cattod.2015.11.029 ↗
8. 10.1016/j.jallcom.2014.12.11510.1016/j.jallcom.2014.12.115 ↗
9. 10.1016/j.jallcom.2006.03.02310.1016/j.jallcom.2006.03.023 ↗
10. 10.1039/C7RA00261K10.1039/C7RA00261K ↗
11. 10.1038/nchem.104810.1038/nchem.1048 ↗
12. 10.1021/ja403761s10.1021/ja403761s ↗
13. 10.1126/science.106105110.1126/science.1061051 ↗
14. 10.1016/j.apcatb.2012.04.01110.1016/j.apcatb.2012.04.011 ↗
15. 10.1021/ie202521310.1021/ie2025213 ↗
16. 10.1039/c3ta10511c10.1039/c3ta10511c ↗
17. 10.1039/c3nr01577g10.1039/c3nr01577g ↗
18. 10.1016/j.ceramint.2020.01.07010.1016/j.ceramint.2020.01.070 ↗
19. 10.1039/C4CS00269E10.1039/C4CS00269E ↗
20. 10.1039/C4TC00988F10.1039/C4TC00988F ↗
21. 10.1039/C6TA08660H10.1039/C6TA08660H ↗
22. 10.1002/ppsc.20150024310.1002/ppsc.201500243 ↗
23. 10.1039/c1dt11147g10.1039/c1dt11147g ↗
24. 10.1039/c2jm30703k10.1039/c2jm30703k ↗
25. 10.1039/C5NR06908D10.1039/C5NR06908D ↗
26. 10.1039/C6EE03442J10.1039/C6EE03442J ↗
27. 10.1016/j.apcatb.2016.01.07010.1016/j.apcatb.2016.01.070 ↗
28. 10.1021/jp961980610.1021/jp9619806 ↗
29. 10.1016/j.jcrysgro.2015.03.01810.1016/j.jcrysgro.2015.03.018 ↗