journal article·2017-06-09Open access

Selenium/Graphite Platelet Nanofiber Composite for Durable Li–Se Batteries

Radha Mukkabla, Sathish Deshagani, Praveen Meduri, Melepurath Deepa, Partha Ghosal

ACS Energy Letters· Volume 2· Issue 6

Abstract

High Resolution Image Download MS PowerPoint Slide Long-lasting Li–Se cells with a Se/graphite platelet nanofiber (GPNF) composite is prepared for the first time, and it shows a reversible capacity of 489 and 384.7 mAh g Se –1 after 200 and 350 charge/discharge cycles, respectively. It shows superior rate capability and low Se polarization even with a high Se (75 wt %) proportion. It also shows higher capacity and better cycling stability compared to conventional Se/carbon material composites (with graphene oxide (GO), reduced GO, and carbon nanotubes). The effectiveness of GPNFs as a conductive support and for inhibiting the shuttle and dissolution of polyselenides in the electrolyte is also confirmed by conducting atomic force microscopy studies. Nanoscale current maps of Se/GPNFs reveal the presence of homogeneously distributed high-current domains, which are retained even after the first discharge. In contrast, the pristine Se electrode is characterized by predominant low-current regions after the first discharge. The ability of GPNFs to enable the preparation of durable and easily processable Li–Se cells is demonstrated.
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Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research

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Affiliations

Defence Metallurgical Research Laboratory, Defence Research and Development Organisation (DRDO), Hyderabad 500058, Telangana, India

Funding

Department of Science and Technology, Ministry of Science and Technology

References (22)

Show source-provided references
1. 10.1016/j.jpowsour.2013.02.05010.1016/j.jpowsour.2013.02.050 ↗
2. 10.1021/cm034703210.1021/cm0347032 ↗
3. 10.1038/ncomms270510.1038/ncomms2705 ↗
4. 10.1016/j.jpowsour.2016.12.06210.1016/j.jpowsour.2016.12.062 ↗
5. 10.1016/j.nanoen.2014.07.01210.1016/j.nanoen.2014.07.012 ↗
6. 10.1016/j.jpowsour.2014.04.02710.1016/j.jpowsour.2014.04.027 ↗
7. 10.1039/c3cc46943c10.1039/c3cc46943c ↗
8. 10.1021/ja211766q10.1021/ja211766q ↗
9. 10.1021/acsami.6b0406010.1021/acsami.6b04060 ↗
10. 10.1039/c4ra00446a10.1039/c4ra00446a ↗
11. 10.1039/C4TA02017K10.1039/C4TA02017K ↗
12. 10.1039/C4NR03705G10.1039/C4NR03705G ↗
13. 10.1021/nn403108w10.1021/nn403108w ↗
14. 10.1002/aenm.20140098110.1002/aenm.201400981 ↗
15. 10.1002/anie.20130314710.1002/anie.201303147 ↗
16. 10.1063/1.337181310.1063/1.3371813 ↗
17. 10.1021/ja002608d10.1021/ja002608d ↗
18. 10.1021/ja402597g10.1021/ja402597g ↗
19. 10.1007/s11051-016-3513-z10.1007/s11051-016-3513-z ↗
20. 10.1039/C4TA03141E10.1039/C4TA03141E ↗
21. 10.1039/C4TA04611K10.1039/C4TA04611K ↗
22. 10.1021/acsenergylett.6b0001510.1021/acsenergylett.6b00015 ↗