journal article·2016-08-31

Role of Graphene Oxide Liquid Crystals in Hydrothermal Reduction and Supercapacitor Performance

Bin Wang, Jinzhang Liu, Yi Zhao, Yan Li, Wei Xian, Mojtaba Amjadipour, Jennifer MacLeod, Nunzio Motta

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Abstract

The formation of liquid crystal (LC) phases in graphene oxide (GO) aqueous solution is utilized to develop high-performance supercapacitors. To investigate the effect of LC formation on the properties of subsequently reduced GO (rGO), we compare films prepared through blade-coating of viscous LC-GO solution and ultrasonic spray-coating of diluted GO aqueous dispersion. After hydrothermal reduction under identical conditions, the films show different morphology, oxygen content, and specific capacitance. Trapped water in the LC GO film plays a role in preventing restacking of sheets and facilitating the removal of oxygenated groups during the reduction process. In device architectures with either liquid or polymer electrolyte, the specific capacitance of the blade-coated film is twice as high as that of the spray-coated one. For a blade-coated film with mass loading of 0.115 mg/cm(2), the specific capacitance reaches 286 F/g in aqueous electrolyte and 263 F/g in gelled electrolyte, respectively. This study suggests a route to pilot-scale production of high-performance graphene supercapacitors through blade-coated LC-GO films.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supercapacitor Materials and Fabrication · Electrospun Nanofibers in Biomedical Applications · Aerogels and thermal insulation

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Materials Science and Engineering, Beihang University, Beijing 100191, China

Siansonic Technology Co. Ltd., Beijing 101111, China

School of Chemistry, Physics, and Mechanical Engineering, Queensland University of Technology, Brisbane 4001, QLD, Australia

Funding

Ministry of Education of the People's Republic of China

References (33)

Show source-provided references
1. 10.1016/j.jpowsour.2006.02.06510.1016/j.jpowsour.2006.02.065 ↗
2. 10.1038/nnano.2014.23310.1038/nnano.2014.233 ↗
3. 10.1016/j.carbon.2011.11.01010.1016/j.carbon.2011.11.010 ↗
4. 10.1021/ja00170a01610.1021/ja00170a016 ↗
5. 10.1021/nn200069w10.1021/nn200069w ↗
6. 10.1002/adfm.20110044810.1002/adfm.201100448 ↗
7. 10.1002/anie.20100469210.1002/anie.201004692 ↗
8. 10.1002/adfm.20130076510.1002/adfm.201300765 ↗
9. 10.1002/adma.20120344810.1002/adma.201203448 ↗
10. 10.1021/nn406026z10.1021/nn406026z ↗
11. 10.1088/0957-4484/27/16/16540210.1088/0957-4484/27/16/165402 ↗
12. 10.1021/nn101187z10.1021/nn101187z ↗
13. 10.1021/acsami.5b1258610.1021/acsami.5b12586 ↗
14. Wang J. D. · Chim. Sin. · 2014 · 30 · 2077
15. 10.1016/j.apsusc.2015.07.19710.1016/j.apsusc.2015.07.197 ↗
16. 10.1002/adma.20130123010.1002/adma.201301230 ↗
17. 10.1021/nn302818j10.1021/nn302818j ↗
18. 10.1021/nn400083610.1021/nn4000836 ↗
19. 10.1021/nn404073410.1021/nn4040734 ↗
20. 10.1021/acs.nanolett.5b0121210.1021/acs.nanolett.5b01212 ↗
21. 10.1038/ncomms555410.1038/ncomms5554 ↗
22. 10.1021/nl200905810.1021/nl2009058 ↗
23. 10.1021/am504206510.1021/am5042065 ↗
24. 10.1039/C5RA13914G10.1039/C5RA13914G ↗
25. 10.1016/j.jpowsour.2014.10.10410.1016/j.jpowsour.2014.10.104 ↗
26. 10.1126/science.121674410.1126/science.1216744 ↗
27. 10.1016/j.nanoen.2014.02.01410.1016/j.nanoen.2014.02.014 ↗
28. 10.1021/nn302147s10.1021/nn302147s ↗
29. 10.1021/nl803857910.1021/nl8038579 ↗
30. 10.1016/j.jpowsour.2014.12.05210.1016/j.jpowsour.2014.12.052 ↗
31. 10.1002/chem.20140477910.1002/chem.201404779 ↗
32. 10.1016/j.nanoen.2015.10.03810.1016/j.nanoen.2015.10.038 ↗
33. 10.1021/cm503784x10.1021/cm503784x ↗