journal article·2018-06

A Flexible and Ultrahigh Energy Density Capacitor via Enhancing Surface/Interface of Carbon Cloth Supported Colloids

Xitong Liang, Kunfeng Chen, Dongfeng Xue

Advanced Energy Materials· Volume 8· Issue 16
Publisher page

Abstract

Abstract Pseudocapacitors are now reaching the energy density limits set by the surface redox reaction of their electrode materials, requiring new cation paradigms for a fast cation Faradaic reaction with high capacitance. In this work, a flexible and ultrahigh energy density capacitor is reported via enhancing surface/interface of active colloids and supported carbon cloth. A flexible asymmetrical capacitor assembled with Ni2+ colloidal cathode and Fe3+ colloidal anode displays a high energy density of 353 W h kg−1 at the power density of 2250 W kg−1, outperforming recent reported pseudocapacitors, and shows superior cycling stability after 10 000 charge–discharge cycles at current density of 30 A g−1. This work demonstrates that the optimized surface/interface of carbon cloth and colloids can lead to the enhancement of both stability and activity of colloidal electrode.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Supercapacitor Materials and Fabrication · Advancements in Battery Materials · Advanced battery technologies research

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

Affiliations

State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun 130022 China

University of Chinese Academy of Sciences Beijing 100049 China

Funding

National Natural Science Foundation of China

References (48)

Show source-provided references
1. 10.1126/science.aam662010.1126/science.aam6620 ↗
2. 10.1002/advs.20160053910.1002/advs.201600539 ↗
3. 10.1002/adma.20090332810.1002/adma.200903328 ↗
4. 10.1038/nmat229710.1038/nmat2297 ↗
5. 10.1126/science.115873610.1126/science.1158736 ↗
6. 10.1038/nenergy.2016.7010.1038/nenergy.2016.70 ↗
7. 10.1039/C5CS00580A10.1039/C5CS00580A ↗
8. Yu M. · Chem. Eur. J. · 2018
9. 10.1002/aenm.20130081610.1002/aenm.201300816 ↗
10. 10.1038/nmat476610.1038/nmat4766 ↗
11. 10.1002/aenm.20170133610.1002/aenm.201701336 ↗
12. Zhu L. · Angew. Chem., Int. Ed. · 2016 · 55 · 9575
13. 10.1126/science.aam585210.1126/science.aam5852 ↗
14. 10.1039/C7EE00977A10.1039/C7EE00977A ↗
15. 10.1002/aenm.20160096910.1002/aenm.201600969 ↗
16. 10.1126/science.aal426310.1126/science.aal4263 ↗
17. 10.1038/nmat480810.1038/nmat4808 ↗
18. 10.1021/acsami.6b1063810.1021/acsami.6b10638 ↗
19. 10.1002/adma.20170038910.1002/adma.201700389 ↗
20. 10.1002/anie.20160952710.1002/anie.201609527 ↗
21. 10.1016/j.nanoen.2017.04.01910.1016/j.nanoen.2017.04.019 ↗
22. 10.1021/acssuschemeng.6b0214410.1021/acssuschemeng.6b02144 ↗
23. 10.1038/s41467-017-00550-310.1038/s41467-017-00550-3 ↗
24. 10.1039/C7CP07473E10.1039/C7CP07473E ↗
25. 10.1002/asia.20170045410.1002/asia.201700454 ↗
26. 10.1002/anie.20170173710.1002/anie.201701737 ↗
27. 10.1002/anie.20120142910.1002/anie.201201429 ↗
28. 10.1021/acsami.6b1410010.1021/acsami.6b14100 ↗
29. 10.1038/nmat360110.1038/nmat3601 ↗
30. 10.1002/adma.20160686010.1002/adma.201606860 ↗
31. 10.1002/adma.20160172310.1002/adma.201601723 ↗
32. 10.1021/jacs.6b1331410.1021/jacs.6b13314 ↗
33. 10.1038/ncomms1458910.1038/ncomms14589 ↗
34. 10.1038/natrevmats.2016.1310.1038/natrevmats.2016.13 ↗
35. 10.1038/nchem.252410.1038/nchem.2524 ↗
36. 10.1088/1361-6528/aa9bfd10.1088/1361-6528/aa9bfd ↗
37. 10.1016/j.apsusc.2016.01.15110.1016/j.apsusc.2016.01.151 ↗
38. 10.1063/1.153057310.1063/1.1530573 ↗
39. 10.1038/ncomms1519210.1038/ncomms15192 ↗
40. 10.1038/ncomms1426410.1038/ncomms14264 ↗
41. 10.1002/adfm.20170101410.1002/adfm.201701014 ↗
42. 10.1002/adfm.20160530710.1002/adfm.201605307 ↗
43. 10.1002/aenm.20160112710.1002/aenm.201601127 ↗
44. 10.1002/adfm.20160672810.1002/adfm.201606728 ↗
45. 10.1002/adma.20170080410.1002/adma.201700804 ↗
46. 10.1002/aenm.20170098310.1002/aenm.201700983 ↗
47. 10.1002/aenm.20170044710.1002/aenm.201700447 ↗
48. 10.1002/adfm.20170084010.1002/adfm.201700840 ↗