Unusual Li‐Storage Behaviour of Two‐Dimensional ReS2 Single Crystals
Source abstract
Abstract
Abstract Unusual Li‐storage properties are observed for two‐dimensional ReS2 compared to its analogue MoS2. First, we prepared ReS2 single crystals (99.9 % crystallinity) by chemical vapour transport with high yield and utmost purity. Li‐storage properties are assessed using a standard half‐cell assembly with metallic Li as the counter electrode. The highly crystalline ReS2 rendered excellent electrochemical characteristics with interesting features. This logically leads to further exploration of ReS2 towards Li‐storage. Indeed, ReS2 could act as efficient intercalation host for Li‐ions with lower redox potential (∼1.2 V vs. Li) and decent reversibility (∼0.4 mol Li). On the other hand, high reversibility is registered while deep discharging of the active material. This eventually obeys the perfect conversion pathway. Interestingly, electrochemically activated ReS2 also rendered good reversibility and eventually serves as an insertion host with a working potential of ∼2 V vs. Li.
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Research context
OpenAlex topics: Advancements in Battery Materials · MXene and MAX Phase Materials · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering Nanyang Technological University Singapore 639798
Department of Physics School of Engineering & Applied Science Bennet University Greater Noida, Uttar Pradesh India
Department of Chemistry Indian Institute of Science Education and Research (IISER) Tirupati- 517507 India
Funding
National Research Foundation of Singapore (NRF) · Science & Engineering Research Board (SERB) · Department of Science & Technology · Govt. of India through Ramanujan Fellowship
References (34)
Show source-provided references
1. 10.1039/C5TA00361J10.1039/C5TA00361J ↗
2. 10.1146/annurev-chembioeng-073009-10094210.1146/annurev-chembioeng-073009-100942 ↗
3. 10.1146/annurev-chembioeng-061010-11411610.1146/annurev-chembioeng-061010-114116 ↗
4. Jiarui H. · Adv. Mater. · 2017 · 29 · 170270710.1002/adma.201702707 ↗
5. 10.1021/acsnano.7b0305710.1021/acsnano.7b03057 ↗
6. 10.1021/acsnano.6b0462210.1021/acsnano.6b04622 ↗
7. 10.1021/acs.jpclett.7b0165310.1021/acs.jpclett.7b01653 ↗
8. 10.1002/aenm.20140222510.1002/aenm.201402225 ↗
9. 10.1039/c2ta01393b10.1039/c2ta01393b ↗
10. 10.1039/c2ee21892e10.1039/c2ee21892e ↗
11. 10.1021/cr500091510.1021/cr5000915 ↗
12. 10.1016/j.mattod.2015.02.01510.1016/j.mattod.2015.02.015 ↗
13. 10.1016/j.cej.2017.01.11110.1016/j.cej.2017.01.111 ↗
14. 10.1039/C6EE03173K10.1039/C6EE03173K ↗
15. 10.1039/C7TA01594A10.1039/C7TA01594A ↗
16. 10.1039/C7TA04470D10.1039/C7TA04470D ↗
17. 10.1039/C7TA08346G10.1039/C7TA08346G ↗
18. Xing O. · Adv. Funct. Mater. · 2017 · 27 · 160624210.1002/adfm.201606242 ↗
19. 10.1002/aenm.20170284110.1002/aenm.201702841 ↗
20. 10.1016/j.apmt.2016.09.00110.1016/j.apmt.2016.09.001 ↗
21. 10.1002/slct.20170218110.1002/slct.201702181 ↗
22. 10.1016/0025-5408(76)90210-510.1016/0025-5408(76)90210-5 ↗
23. 10.1016/0378-7753(93)80192-R10.1016/0378-7753(93)80192-R ↗
24. 10.1039/C3EE42591F10.1039/C3EE42591F ↗
25. 10.1016/S0022-3697(99)00201-210.1016/S0022-3697(99)00201-2 ↗
26. 10.1021/acs.chemmater.6b0036410.1021/acs.chemmater.6b00364 ↗
27. 10.1002/aenm.20160260710.1002/aenm.201602607 ↗
28. 10.1038/3503504510.1038/35035045 ↗
29. 10.1021/nl202675f10.1021/nl202675f ↗
30. 10.1016/j.electacta.2012.07.02010.1016/j.electacta.2012.07.020 ↗
31. 10.1002/adma.20150549810.1002/adma.201505498 ↗
32. 10.1016/j.cej.2017.01.00410.1016/j.cej.2017.01.004 ↗
33. 10.1007/s10853-016-0500-910.1007/s10853-016-0500-9 ↗
34. 10.1016/j.apsusc.2017.03.29610.1016/j.apsusc.2017.03.296 ↗