Rational Design of Hierarchical Carbon/Mesoporous Silicon Composite Sponges as High-Performance Flexible Energy Storage Electrodes
Source abstract
Abstract
Nanostructuring silicon (Si) and combining Si with carbon shells have been studied in recent Li-ion battery electrodes, yet it remains a grand challenge to overcome the low electrical conductivity and associated volume change of Si. Here, by first coating a mesoporous SiO 2 (meso-SiO 2 ) onto carbon nanotube (CNT) networks and then converting it into a meso-Si layer covered by carbon, we obtained a freestanding, highly porous composite sponge electrode consisting of three-dimensionally interconnected sandwiched carbon-Si-CNT skeletons. In this hierarchical structure, the macropores among the sponge connect to mesopores in the meso-Si layer so that Li + diffusion is facilitated, whereas the underlying CNT networks serve as conductive paths for electrons transport. Meanwhile, the outer carbon coating on meso-Si could buffer the volume expansion and prevent material shedding. As a result, our sandwiched carbon-Si-CNT electrodes exhibit large specific capacity, high rate capability and long cycle life. The combination of carbon-wrapped meso-Si and CNT sponges might be a potential strategy for developing efficient electrodes in various energy storage systems.
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
Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China
Department of Materials Science and Engineering, College of Engineering, Peking University, Beijing 100871, China
Funding
National Natural Science Foundation of China · Central Committee of the Communist Party of China · Wuhan Municipality
References (38)
Show source-provided references
1. 10.1038/nmat272510.1038/nmat2725 ↗
2. 10.1073/pnas.130502511010.1073/pnas.1305025110 ↗
3. 10.1002/adma.20140248410.1002/adma.201402484 ↗
4. 10.1021/nl201470j10.1021/nl201470j ↗
5. 10.1002/adma.20130179510.1002/adma.201301795 ↗
6. 10.1038/nchem.180210.1038/nchem.1802 ↗
7. 10.1002/aenm.20130049610.1002/aenm.201300496 ↗
8. 10.1016/j.nanoen.2016.04.04310.1016/j.nanoen.2016.04.043 ↗
9. 10.1002/adfm.20150233010.1002/adfm.201502330 ↗
10. 10.1039/C4NR03948C10.1039/C4NR03948C ↗
11. 10.1002/adma.20130084410.1002/adma.201300844 ↗
12. 10.1002/adma.20130431910.1002/adma.201304319 ↗
13. 10.1002/adma.20130153010.1002/adma.201301530 ↗
14. 10.1016/j.carbon.2013.03.01710.1016/j.carbon.2013.03.017 ↗
15. 10.1016/j.elecom.2011.02.01210.1016/j.elecom.2011.02.012 ↗
16. 10.1021/nn100619m10.1021/nn100619m ↗
17. 10.1002/smll.20140008810.1002/smll.201400088 ↗
18. 10.1021/nn901632g10.1021/nn901632g ↗
19. 10.1002/adma.20130192010.1002/adma.201301920 ↗
20. 10.1002/celc.20150032310.1002/celc.201500323 ↗
21. 10.1021/nn305202310.1021/nn3052023 ↗
22. 10.1039/c3nr33683b10.1039/c3nr33683b ↗
23. 10.1002/adma.20140281310.1002/adma.201402813 ↗
24. 10.1002/adma.20090298610.1002/adma.200902986 ↗
25. 10.1039/c3nr05931f10.1039/c3nr05931f ↗
26. 10.1007/s12274-016-1106-x10.1007/s12274-016-1106-x ↗
27. 10.1021/nn303393p10.1021/nn303393p ↗
28. 10.1002/adma.20140193710.1002/adma.201401937 ↗
29. 10.1002/aenm.20110076510.1002/aenm.201100765 ↗
30. 10.1002/anie.20080435510.1002/anie.200804355 ↗
31. 10.1073/pnas.160381011310.1073/pnas.1603810113 ↗
32. 10.1039/C7EE00244K10.1039/C7EE00244K ↗
33. 10.1038/nenergy.2016.11310.1038/nenergy.2016.113 ↗
34. 10.1002/aenm.20110005610.1002/aenm.201100056 ↗
35. 10.1002/adma.20110304410.1002/adma.201103044 ↗
36. 10.1002/ange.20131041210.1002/ange.201310412 ↗
37. 10.1002/aenm.20120038910.1002/aenm.201200389 ↗
38. 10.1002/aenm.20110048510.1002/aenm.201100485 ↗