Pyroprotein-Derived Hard Carbon Fibers Exhibiting Exceptionally High Plateau Capacities for Sodium Ion Batteries
Source abstract
Abstract
In this study, low-density, hard-carbon fibers incorporating multitudinous closed pores with few-nanometer-scale widths were prepared from waste silk fabric by a simple high-temperature heating process (2000 °C). The pyroprotein carbon fibers exhibited a significantly high single-plateau capacity of 300 mA h g–1 at ∼0.1 V Na+/Na, a high initial Coulombic efficiency of ∼91.9%, and stable cycling behaviors of more than 200 cycles when used as the anode of a sodium-ion battery. Characterization using in situ X-ray diffraction patterns and ex situ field-emission transmission electron microscopy confirmed that the outstanding charge storage behaviors of the pyroprotein carbon fibers are based on sodium–metal nanoclustering in the closed pores. Moreover, full cells assembled with the pyroprotein carbon-fiber-based anode and a reported cathode demonstrated their practical electrochemical performances, including a specific energy of 262 Wh kg–1.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Advanced Composite Materials, Korea Institute of Science and Technology (KIST), Jeonbuk 55324, South Korea
Department of Polymer Science and Engineering, Inha University, Incheon 22212, South Korea
Department of Chemical Engineering, Kangwon National University, Samcheok 25913, South Korea
Funding
National Research Foundation of Korea
References (36)
Show source-provided references
1. 10.1038/nchem.208510.1038/nchem.2085 ↗
2. 10.1038/nmat483410.1038/nmat4834 ↗
3. 10.1021/cr500192f10.1021/cr500192f ↗
4. 10.1002/adfm.20120069110.1002/adfm.201200691 ↗
5. 10.1016/j.carbon.2015.12.04710.1016/j.carbon.2015.12.047 ↗
6. 10.1002/aenm.20180007910.1002/aenm.201800079 ↗
7. 10.1002/aenm.20160094310.1002/aenm.201600943 ↗
8. 10.1149/1.137956510.1149/1.1379565 ↗
9. 10.1002/adfm.20110085410.1002/adfm.201100854 ↗
10. 10.1002/aenm.20170278110.1002/aenm.201702781 ↗
11. 10.1021/acsami.8b0838010.1021/acsami.8b08380 ↗
12. 10.1021/acsami.5b0086110.1021/acsami.5b00861 ↗
13. 10.1149/2.0771608jes10.1149/2.0771608jes ↗
14. 10.1021/acsomega.7b0025910.1021/acsomega.7b00259 ↗
15. 10.1002/aenm.20170040310.1002/aenm.201700403 ↗
16. 10.1002/aenm.20160289410.1002/aenm.201602894 ↗
17. 10.1021/acs.nanolett.5b0196910.1021/acs.nanolett.5b01969 ↗
18. 10.1016/j.nanoen.2017.12.01310.1016/j.nanoen.2017.12.013 ↗
19. 10.1002/aenm.20170062910.1002/aenm.201700629 ↗
20. 10.1002/adma.20150230310.1002/adma.201502303 ↗
21. 10.1002/aenm.20160065910.1002/aenm.201600659 ↗
22. 10.1002/aenm.20150158810.1002/aenm.201501588 ↗
23. 10.1002/aenm.20170321710.1002/aenm.201703217 ↗
24. 10.1002/aenm.20170326810.1002/aenm.201703268 ↗
25. 10.1038/ncomms814510.1038/ncomms8145 ↗
26. 10.1016/j.jpowsour.2017.12.05410.1016/j.jpowsour.2017.12.054 ↗
27. 10.1038/s41467-017-00132-310.1038/s41467-017-00132-3 ↗
28. 10.1016/j.jpowsour.2016.09.09110.1016/j.jpowsour.2016.09.091 ↗
29. 10.1021/am404788e10.1021/am404788e ↗
30. 10.1002/anie.20140373410.1002/anie.201403734 ↗
31. 10.1039/C5EE02051D10.1039/C5EE02051D ↗
32. 10.1021/ja406016j10.1021/ja406016j ↗
33. 10.1002/aenm.20170240910.1002/aenm.201702409 ↗
34. 10.1039/C7TA01895A10.1039/C7TA01895A ↗
35. 10.1002/smll.20170076710.1002/smll.201700767 ↗
36. 10.1021/nn300920e10.1021/nn300920e ↗