journal article·2019-06-05

Green Synthesis of Dual Carbon Conductive Network-Encapsulated Hollow SiOx Spheres for Superior Lithium-Ion Batteries

Tao Xu, Qian Wang, Jian Zhang, Xiaohua Xie, Baojia Xia

ACS Applied Materials & Interfaces· Volume 11· Issue 22
Publisher page

Abstract

Designing hollow/porous structure is regarded as an effective approach to address the dramatic volumetric variation issue for Si-based anode materials in Li-ion batteries (LIBs). Pioneer studies mainly focused on acid/alkali etching to create hollow/porous structures, which are, however, highly corrosive and may lead to a complicated synthetic process. In this paper, a dual carbon conductive network-encapsulated hollow SiOx (DC-HSiOx) is fabricated through a green route, where polyacrylic acid is adopted as an eco-friendly soft template. Low electrical resistance and integrated electrode structure can be maintained during cycles because of the dual carbon conductive networks distributed both on the surface of single particles formed by amorphous carbon and among particles constructed by reduced graphene oxide. Importantly, the hollow space is reserved within SiOx spheres to accommodate the huge volumetric variation and shorten the transport pathway of Li+ ions. As a result, the DC-HSiOx composite delivers a large reversible capacity of 1113 mA h g–1 at 0.1 A g–1, an excellent cycling performance up to 300 cycles with a capacity retention of 92.5% at 0.5 A g–1, and a good rate capability. Furthermore, the DC-HSiOx//LiNi0.8Co0.1Mn0.1O2 full cell exhibits high energy density (419 W h kg–1) and superior cycling performance. These results render an opportunity for the unique DC-HSiOx composite as a potential anode material for use in high-performance LIBs.
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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

Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050, China

University of Chinese Academy of Sciences, Beijing 100049, China

School of Physical and Mathematical Sciences, Nanjing Tech University, Nanjing 211800, China

Funding

National Natural Science Foundation of China

References (55)

Show source-provided references
1. 10.1039/c1ee01388b10.1039/c1ee01388b ↗
2. 10.1002/adma.20109011610.1002/adma.201090116 ↗
3. 10.1016/j.nanoen.2016.11.01310.1016/j.nanoen.2016.11.013 ↗
4. 10.1021/jp204653y10.1021/jp204653y ↗
5. 10.1002/adma.20140057810.1002/adma.201400578 ↗
6. 10.1016/j.nanoen.2016.04.04310.1016/j.nanoen.2016.04.043 ↗
7. 10.1016/j.nanoen.2017.07.00710.1016/j.nanoen.2017.07.007 ↗
8. 10.1016/j.ensm.2018.04.00810.1016/j.ensm.2018.04.008 ↗
9. 10.1016/j.jpowsour.2010.07.02010.1016/j.jpowsour.2010.07.020 ↗
10. 10.1016/j.nantod.2012.08.00410.1016/j.nantod.2012.08.004 ↗
11. 10.1021/nl201470j10.1021/nl201470j ↗
12. 10.1021/nl201684d10.1021/nl201684d ↗
13. 10.1002/anie.20090628710.1002/anie.200906287 ↗
14. 10.1039/c8cs00441b10.1039/c8cs00441b ↗
15. 10.1039/c8ta03987a10.1039/c8ta03987a ↗
16. 10.1002/admi.20180163110.1002/admi.201801631 ↗
17. 10.1039/c6ra25714c10.1039/c6ra25714c ↗
18. 10.1021/acs.jpcc.5b1058910.1021/acs.jpcc.5b10589 ↗
19. 10.1016/j.jpowsour.2017.07.07310.1016/j.jpowsour.2017.07.073 ↗
20. 10.1016/j.jpowsour.2012.08.06010.1016/j.jpowsour.2012.08.060 ↗
21. 10.2109/jcersj2.119.85510.2109/jcersj2.119.855 ↗
22. 10.1016/j.jelechem.2011.08.01010.1016/j.jelechem.2011.08.010 ↗
23. 10.1002/adma.20140119410.1002/adma.201401194 ↗
24. 10.1021/acs.nanolett.5b0377610.1021/acs.nanolett.5b03776 ↗
25. 10.1038/ncomms608810.1038/ncomms6088 ↗
26. 10.1016/j.jpowsour.2017.02.06110.1016/j.jpowsour.2017.02.061 ↗
27. 10.1073/pnas.160381011310.1073/pnas.1603810113 ↗
28. 10.1016/j.electacta.2016.08.05910.1016/j.electacta.2016.08.059 ↗
29. 10.1002/anie.20110788510.1002/anie.201107885 ↗
30. 10.1021/cm303338v10.1021/cm303338v ↗
31. 10.1016/j.jpowsour.2017.01.12510.1016/j.jpowsour.2017.01.125 ↗
32. 10.1039/c5nr01209k10.1039/c5nr01209k ↗
33. 10.1039/c5cp01212k10.1039/c5cp01212k ↗
34. 10.1016/j.jpowsour.2013.01.02910.1016/j.jpowsour.2013.01.029 ↗
35. 10.1016/j.electacta.2014.12.12410.1016/j.electacta.2014.12.124 ↗
36. 10.1016/j.jpowsour.2016.01.10610.1016/j.jpowsour.2016.01.106 ↗
37. 10.1039/c5ta00457h10.1039/c5ta00457h ↗
38. 10.1021/acsami.8b1813410.1021/acsami.8b18134 ↗
39. 10.1002/adma.20170743010.1002/adma.201707430 ↗
40. 10.1021/acsami.5b0123010.1021/acsami.5b01230 ↗
41. 10.1021/acs.jpcc.7b0587610.1021/acs.jpcc.7b05876 ↗
42. 10.1021/acs.nanolett.7b0090610.1021/acs.nanolett.7b00906 ↗
43. 10.1021/jp710990b10.1021/jp710990b ↗
44. 10.1016/j.colsurfa.2018.03.03310.1016/j.colsurfa.2018.03.033 ↗
45. 10.1016/j.jpowsour.2014.10.07710.1016/j.jpowsour.2014.10.077 ↗
46. 10.1016/j.electacta.2014.11.14910.1016/j.electacta.2014.11.149 ↗
47. 10.1016/j.jpowsour.2011.01.05310.1016/j.jpowsour.2011.01.053 ↗
48. 10.1016/j.ensm.2018.01.00410.1016/j.ensm.2018.01.004 ↗
49. 10.1002/adfm.20170523510.1002/adfm.201705235 ↗
50. 10.1016/j.jpowsour.2013.02.07710.1016/j.jpowsour.2013.02.077 ↗
51. 10.1149/2.0911414jes10.1149/2.0911414jes ↗
52. 10.1038/nnano.2014.610.1038/nnano.2014.6 ↗
53. 10.1039/c8nr04587a10.1039/c8nr04587a ↗
54. 10.1002/adfm.20130376610.1002/adfm.201303766 ↗
55. 10.1002/adma.20160565010.1002/adma.201605650 ↗