journal article·2021-11-22Open access

Polypeptoid Material as an Anchoring Material for Li–S Batteries

Deobrat Singh, Rajeev Ahuja

ACS Applied Energy Materials· Volume 4· Issue 11

Abstract

Nowadays, lithium-sulfur (Li-S) batteries have attracted considerable attention as a potential candidate for next-generation rechargeable batteries due to their high theoretical specific energy and environmental friendliness. One of the main problems with Li-S batteries is that the lithium polysulfides (LiPSs) easily decompose in the electrolyte which is known as the shuttle effect. Recently, the polypeptoid nanosheet crystal structure has been experimentally synthesized which is very useful for tremendous advances in soft material imaging as well as enabling to design biomimetic nanomaterials. Due to the very interesting properties of the polypeptoid material, we have investigated the electronic structure and charge-transfer mechanism for the lithium-sulfur batteries for the cathode material. The calculated adsorption energies of LiPSs on the surface of the polypeptoid material are in the range of -4.41 to -4.64 and -0.91 eV for the sulfur clusters. Also, the adsorption energies between the interaction of LiPSs and electrolytes (DME and DOL) are 0.75-0.89 eV. It means that the polypeptoid material could suppress the shuttle effect of LiPSs and significantly enhance the cycling performance of Li-S batteries. From these investigated results, the polypeptoid material will be a promising anchoring material for Li-S batteries.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Chemical Synthesis and Characterization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Condensed Matter Theory Group, Materials Theory Division, Department of Physics and Astronomy, Uppsala University, Box 516, 75120 Uppsala, Sweden

Department of Physics, Indian Institute of Technology Ropar, Rupnagar 140001, Punjab, India

Funding

Vetenskapsr??det · J. Gustaf Richert Stiftelse

References (56)

Show source-provided references
1. 10.1021/acs.nanolett.9b0103310.1021/acs.nanolett.9b01033 ↗
2. 10.1021/acsami.6b0469710.1021/acsami.6b04697 ↗
3. 10.1021/acsenergylett.7b0069210.1021/acsenergylett.7b00692 ↗
4. 10.1039/d0ta06537d10.1039/d0ta06537d ↗
5. 10.1016/j.rser.2018.03.00210.1016/j.rser.2018.03.002 ↗
6. 10.1002/chem.20130168910.1002/chem.201301689 ↗
7. 10.1039/c5cc09935h10.1039/c5cc09935h ↗
8. 10.1007/s41918-018-0010-310.1007/s41918-018-0010-3 ↗
9. 10.1002/aenm.20160254310.1002/aenm.201602543 ↗
10. 10.1149/1.180639410.1149/1.1806394 ↗
11. 10.1021/nl202768410.1021/nl2027684 ↗
12. 10.1134/s102319350805002910.1134/s1023193508050029 ↗
13. 10.1021/nn400391h10.1021/nn400391h ↗
14. 10.1016/j.jechem.2017.10.02110.1016/j.jechem.2017.10.021 ↗
15. 10.1021/acsami.8b1903410.1021/acsami.8b19034 ↗
16. 10.1021/nl200658a10.1021/nl200658a ↗
17. 10.1016/j.electacta.2011.03.00510.1016/j.electacta.2011.03.005 ↗
18. Navaneedhakrishnan J. · 2011 · 341
19. 10.1021/acsenergylett.7b0023010.1021/acsenergylett.7b00230 ↗
20. 10.1021/acsenergylett.7b0069710.1021/acsenergylett.7b00697 ↗
21. 10.1021/acsenergylett.6b0010410.1021/acsenergylett.6b00104 ↗
22. 10.1021/acsenergylett.6b0024510.1021/acsenergylett.6b00245 ↗
23. 10.1016/j.jechem.2016.11.00310.1016/j.jechem.2016.11.003 ↗
24. 10.1002/aenm.20177014110.1002/aenm.201770141 ↗
25. 10.1021/jp111472410.1021/jp1114724 ↗
26. 10.1002/aenm.20120001710.1002/aenm.201200017 ↗
27. 10.1039/c3cc38009b10.1039/c3cc38009b ↗
28. 10.1002/adma.20160681710.1002/adma.201606817 ↗
29. 10.1002/adma.20160217210.1002/adma.201602172 ↗
30. 10.1007/s11051-016-3364-710.1007/s11051-016-3364-7 ↗
31. 10.1073/pnas.190999211610.1073/pnas.1909992116 ↗
32. 10.1016/j.apsusc.2018.04.13710.1016/j.apsusc.2018.04.137 ↗
33. 10.1103/physrevb.59.175810.1103/physrevb.59.1758 ↗
34. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
35. 10.1103/physrevb.54.1116910.1103/physrevb.54.11169 ↗
36. 10.1103/physrevb.50.1795310.1103/physrevb.50.17953 ↗
37. 10.1103/physrevlett.77.386510.1103/physrevlett.77.3865 ↗
38. 10.1063/1.338234410.1063/1.3382344 ↗
39. 10.1002/jcc.2175910.1002/jcc.21759 ↗
40. 10.1107/s002188980801201610.1107/s0021889808012016 ↗
41. 10.1063/1.472802610.1063/1.4728026 ↗
42. 10.1063/1.132322410.1063/1.1323224 ↗
43. 10.1063/1.132967210.1063/1.1329672 ↗
44. 10.1063/1.46394010.1063/1.463940 ↗
45. 10.1016/j.commatsci.2005.04.01010.1016/j.commatsci.2005.04.010 ↗
46. 10.1103/physrevb.86.24540510.1103/physrevb.86.245405 ↗
47. 10.1038/s41524-020-0273-110.1038/s41524-020-0273-1 ↗
48. 10.1021/cr500062v10.1021/cr500062v ↗
49. 10.1149/1.341400110.1149/1.3414001 ↗
50. 10.1039/d0ta04187d10.1039/d0ta04187d ↗
51. 10.1021/acs.nanolett.5b0036710.1021/acs.nanolett.5b00367 ↗
52. 10.1039/c6ta00871b10.1039/c6ta00871b ↗
53. 10.1021/acsami.0c2113610.1021/acsami.0c21136 ↗
54. 10.1038/ncomms1120310.1038/ncomms11203 ↗
55. 10.1021/jp410969u10.1021/jp410969u ↗
56. 10.1073/pnas.161583711410.1073/pnas.1615837114 ↗