Laser Reduction of Nitrogen-Rich Carbon Nanoparticles@Graphene Oxides Composites for High Rate Performance Supercapacitors
Source abstract
Abstract
Nitrogen-doped graphene or graphene derivatives have been proven superior electrode materials for high-performance supercapacitors. Synchronous N doping and reduction of graphene oxide (GO) is an effective approach to prepare such electrode materials. However, current strategies are limited to the use of liquid or vapor doping agents, making the preparation process complex and less environmentally friendly. We here report a facile way to prepare nitrogen-rich carbon nanoparticles (NCNPs), which can be employed as a solid-state doping agent for efficient N-doping of GO through direct laser writing photoreduction. The doping degree was tuned by varying the mass ratios of the NCNPs in the composites. After laser treatment, the composites show N concentration as high as 7.78 atom %. With the N-doped graphene composites as electrodes, the as-fabricated supercapacitors show high rate performance and obvious enhanced capacitance, revealing great potential for energy storage and conversion devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Graphene research and applications · Graphene and Nanomaterials Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Bionic Engineering (Ministry of Education), Jilin University, Changchun 130022, China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (30)
Show source-provided references
1. 10.1039/C5TA03186A10.1039/C5TA03186A ↗
2. Shukla A. K. · Curr. Sci. · 2000 · 79 · 1656
3. 10.1038/nmat229710.1038/nmat2297 ↗
4. 10.1016/j.cej.2014.02.02310.1016/j.cej.2014.02.023 ↗
5. 10.1016/j.jpowsour.2017.04.10810.1016/j.jpowsour.2017.04.108 ↗
6. 10.1021/nl102661q10.1021/nl102661q ↗
7. 10.1063/1.364141910.1063/1.3641419 ↗
8. 10.1002/adma.20100287210.1002/adma.201002872 ↗
9. 10.1002/smll.20090206610.1002/smll.200902066 ↗
10. 10.1088/0957-4484/22/36/36560110.1088/0957-4484/22/36/365601 ↗
11. 10.1038/nnano.2009.6710.1038/nnano.2009.67 ↗
12. 10.1021/nn901587x10.1021/nn901587x ↗
13. 10.1016/j.carbon.2011.05.04710.1016/j.carbon.2011.05.047 ↗
14. 10.1126/science.117124510.1126/science.1171245 ↗
15. 10.1038/ncomms129110.1038/ncomms1291 ↗
16. 10.1021/nn700375n10.1021/nn700375n ↗
17. 10.1038/nnano.2011.11010.1038/nnano.2011.110 ↗
18. 10.1126/science.121674410.1126/science.1216744 ↗
19. 10.1002/cssc.20150012210.1002/cssc.201500122 ↗
20. 10.1002/adfm.20080110010.1002/adfm.200801100 ↗
21. 10.1039/C2TA00028H10.1039/C2TA00028H ↗
22. 10.1039/C4CS00141A10.1039/C4CS00141A ↗
23. 10.1016/S0008-6223(00)00121-410.1016/S0008-6223(00)00121-4 ↗
24. 10.1039/C6TA01314G10.1039/C6TA01314G ↗
25. 10.1021/nl200905810.1021/nl2009058 ↗
26. 10.1002/adom.20130040110.1002/adom.201300401 ↗
27. 10.1002/adfm.20140029610.1002/adfm.201400296 ↗
28. 10.1016/j.electacta.2017.06.09210.1016/j.electacta.2017.06.092 ↗
29. 10.1016/j.jpowsour.2016.10.09110.1016/j.jpowsour.2016.10.091 ↗
30. 10.1039/C4TA03192J10.1039/C4TA03192J ↗