Co@N-Doped Carbon Frameworks Anchored on Graphene as High-Rate and Long-Lifespan Anode Materials for Advanced Li-Ion Hybrid Capacitors
Source abstract
Abstract
Li-ion hybrid capacitors (LIHC) are becoming a prospective candidate for energy storage and can achieve high energy density and power density at the same time. As it uses a battery-type anode, improving its sluggish charge–discharge mechanism becomes important in the LIHC study. Herein, we report a solvothermal method to fabricate Co@N-doped carbon frameworks anchored to graphene (Co-NCF/G) as an anode material for LIHC. Co nanoparticles are generated in the heterohedral carbon matrix with N-doping, and the heterohedral Co@N-doped carbon frameworks were uniformly decorated within three-dimensional (3D) graphene networks. The existence of Co ultrafine nanoparticles and N element can greatly increase the conductivity of Co-NCF/G, and thus strengthen its electrochemical properties. Moreover, the high surface area and effective pore structure formed by graphene networks can shorten the Li-ion transfer route, enhancing the reaction kinetics of the electrode. The device assembled using Co-NCF/G as the anode and active carbon as the cathode exhibits a high specific capacity of 579.5 mAh g–1 after 100 cycles at a current density of 0.5 A g–1, and also delivers a high energy density of 77.17 Wh kg–1 at a high power density of 6801 W kg–1 and long cycling stability with an energy retention of 78.7% after 2000 cycles at a high current density of 5.0 A g–1.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Supercapacitor Materials and Fabrication · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Metallurgy and Environment, Central South University, Changsha 410083, P. R. China
Funding
National Natural Science Foundation of China
References (36)
Show source-provided references
1. 10.1016/j.electacta.2017.03.11010.1016/j.electacta.2017.03.110 ↗
2. 10.1002/adma.20170209310.1002/adma.201702093 ↗
3. 10.1016/j.carbon.2020.01.04510.1016/j.carbon.2020.01.045 ↗
4. 10.1021/acs.chemrev.8b0011610.1021/acs.chemrev.8b00116 ↗
5. 10.1002/aenm.20160080210.1002/aenm.201600802 ↗
6. 10.1021/cr500091510.1021/cr5000915 ↗
7. 10.1039/C9TA01246J10.1039/C9TA01246J ↗
8. 10.1016/j.jpowsour.2016.08.08810.1016/j.jpowsour.2016.08.088 ↗
9. 10.1002/aenm.20180287810.1002/aenm.201802878 ↗
10. 10.1016/j.jpowsour.2018.12.08910.1016/j.jpowsour.2018.12.089 ↗
11. 10.1039/C9TA08676E10.1039/C9TA08676E ↗
12. 10.3390/ma1004041410.3390/ma10040414 ↗
13. 10.1021/acs.nanolett.0c0094310.1021/acs.nanolett.0c00943 ↗
14. 10.1021/acs.accounts.6b0046010.1021/acs.accounts.6b00460 ↗
15. 10.1002/aenm.20180071610.1002/aenm.201800716 ↗
16. 10.1016/j.ccr.2019.05.00610.1016/j.ccr.2019.05.006 ↗
17. 10.1002/adma.20150078310.1002/adma.201500783 ↗
18. 10.1016/j.matlet.2017.04.01610.1016/j.matlet.2017.04.016 ↗
19. 10.1016/j.jallcom.2017.02.27910.1016/j.jallcom.2017.02.279 ↗
20. 10.1007/s12274-013-0334-610.1007/s12274-013-0334-6 ↗
21. 10.1039/C7TA01113J10.1039/C7TA01113J ↗
22. 10.1021/acssuschemeng.9b0064110.1021/acssuschemeng.9b00641 ↗
23. 10.1021/acsami.7b0345210.1021/acsami.7b03452 ↗
24. 10.1021/ja01539a01710.1021/ja01539a017 ↗
25. 10.1038/srep4510510.1038/srep45105 ↗
26. 10.1016/j.electacta.2015.02.01910.1016/j.electacta.2015.02.019 ↗
27. 10.1016/j.jpowsour.2018.08.01310.1016/j.jpowsour.2018.08.013 ↗
28. 10.1039/c3ee44164d10.1039/c3ee44164d ↗
29. 10.1039/C8DT02082E10.1039/C8DT02082E ↗
30. 10.1007/s12274-020-2811-z10.1007/s12274-020-2811-z ↗
31. 10.1038/nmat502910.1038/nmat5029 ↗
32. 10.1021/acsami.9b0635410.1021/acsami.9b06354 ↗
33. 10.1002/adfm.20190053210.1002/adfm.201900532 ↗
34. 10.1002/adma.20160421910.1002/adma.201604219 ↗
35. 10.1007/s12274-017-1753-610.1007/s12274-017-1753-6 ↗
36. 10.1021/nn501972w10.1021/nn501972w ↗