Toward a Reversible Calcium‐Sulfur Battery with a Lithium‐Ion Mediation Approach
Source abstract
Abstract
Abstract Calcium represents a promising anode for the development of high‐energy‐density, low‐cost batteries. However, a lack of suitable electrolytes has restricted the development of rechargeable batteries with a Ca anode. Furthermore, to achieve a high energy density system, sulfur would be an ideal cathode to couple with the Ca anode. Unfortunately, a reversible calcium‐sulfur (Ca‐S) battery has not yet been reported. Herein, a basic study of a reversible nonaqueous room‐temperature Ca‐S battery is presented. The reversibility of the Ca‐S chemistry and high utilization of the sulfur cathode are enabled by employing a Li+‐ion‐mediated calcium‐based electrolyte. Mechanistic insights pursued by spectroscopic, electrochemical, microscopic, and theoretical simulation (density functional theory) investigations imply that the Li+‐ions in the Ca‐electrolyte stimulate the reactivation of polysulfide/sulfide species. The coordination of lithium to sulfur reduces the formation of sturdy Ca‐S ionic bonds, thus boosting the reversibility of the Ca‐S chemistry. In addition, the presence of Li+‐ions facilitates the ionic charge transfer both in the electrolyte and across the solid electrolyte interphase layer, consequently reducing the interfacial and bulk impedance of Ca‐S batteries. As a result, both the utilization of active sulfur in the cathode and the discharge voltage of Ca‐S batteries are significantly improved.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advanced battery technologies research · Thermal Expansion and Ionic Conductivity
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Materials Science & Engineering Program and Texas Materials Institute The University of Texas at Austin Austin TX 78712 USA
McKetta Department of Chemical Engineering The University of Texas at Austin Austin TX 78712 USA
Funding
U.S. Department of Energy · Welch Foundation
References (59)
Show source-provided references
1. 10.1016/j.chempr.2018.05.00910.1016/j.chempr.2018.05.009 ↗
2. 10.1021/cr500049y10.1021/cr500049y ↗
3. 10.1038/s41557-018-0045-410.1038/s41557-018-0045-4 ↗
4. 10.1002/smtd.20170021710.1002/smtd.201700217 ↗
5. 10.1038/nmat446210.1038/nmat4462 ↗
6. 10.1149/2.0811508jes10.1149/2.0811508jes ↗
7. 10.1149/1.212776810.1149/1.2127768 ↗
8. 10.1021/acs.chemmater.5b0234210.1021/acs.chemmater.5b02342 ↗
9. 10.1016/S0378-7753(03)00307-010.1016/S0378-7753(03)00307-0 ↗
10. 10.1016/0378-7753(89)80062-X10.1016/0378-7753(89)80062-X ↗
11. 10.1016/0378-7753(89)80057-610.1016/0378-7753(89)80057-6 ↗
12. 10.1016/j.elecom.2016.03.01610.1016/j.elecom.2016.03.016 ↗
13. 10.1016/j.jpowsour.2014.09.10110.1016/j.jpowsour.2014.09.101 ↗
14. 10.14447/jnmes.v19i2.23110.14447/jnmes.v19i2.231 ↗
15. 10.1021/acs.jpcc.5b1024510.1021/acs.jpcc.5b10245 ↗
16. 10.1016/j.electacta.2016.04.15910.1016/j.electacta.2016.04.159 ↗
17. 10.1021/acs.chemmater.5b0402710.1021/acs.chemmater.5b04027 ↗
18. 10.1021/cr500062v10.1021/cr500062v ↗
19. 10.1002/smll.20140325710.1002/smll.201403257 ↗
20. 10.1021/jacs.7b0337910.1021/jacs.7b03379 ↗
21. 10.1021/jacs.7b0338010.1021/jacs.7b03380 ↗
22. 10.1021/ja409705u10.1021/ja409705u ↗
23. 10.1021/acs.accounts.7b0046010.1021/acs.accounts.7b00460 ↗
24. 10.1021/acs.chemmater.5b0458810.1021/acs.chemmater.5b04588 ↗
25. 10.1021/acsenergylett.7b0071410.1021/acsenergylett.7b00714 ↗
26. 10.1021/jacs.6b0868510.1021/jacs.6b08685 ↗
27. 10.1021/acsenergylett.6b0021310.1021/acsenergylett.6b00213 ↗
28. 10.1002/aenm.20140115510.1002/aenm.201401155 ↗
29. 10.1021/jacs.5b0782010.1021/jacs.5b07820 ↗
30. 10.1021/ic500919e10.1021/ic500919e ↗
31. 10.1016/j.ensm.2018.06.02010.1016/j.ensm.2018.06.020 ↗
32. 10.1002/aenm.20170056110.1002/aenm.201700561 ↗
33. 10.1002/anie.20160353110.1002/anie.201603531 ↗
34. 10.1016/j.chempr.2017.12.02910.1016/j.chempr.2017.12.029 ↗
35. 10.1002/aenm.20130016010.1002/aenm.201300160 ↗
36. 10.1149/1.208545510.1149/1.2085455 ↗
37. 10.1149/1.210853310.1149/1.2108533 ↗
38. 10.1002/advs.20170108210.1002/advs.201701082 ↗
39. 10.1149/1.218600310.1149/1.2186003 ↗
40. 10.1002/aenm.20140150710.1002/aenm.201401507 ↗
41. 10.1021/jp507655u10.1021/jp507655u ↗
42. 10.1039/C6MH00043F10.1039/C6MH00043F ↗
43. 10.1021/jp501320810.1021/jp5013208 ↗
44. 10.1021/ic50126a04710.1021/ic50126a047 ↗
45. 10.1039/C4CP04895D10.1039/C4CP04895D ↗
46. 10.1002/chem.20140534410.1002/chem.201405344 ↗
47. 10.1021/jp208159v10.1021/jp208159v ↗
48. 10.1002/(SICI)1096-9918(199908)28:1<101::AID-SIA627>3.0.CO;2-010.1002/(SICI)1096-9918(199908)28:1<101::AID-SIA627>3.0.CO;2-0 ↗
49. 10.1021/jz502110810.1021/jz5021108 ↗
50. 10.1002/aenm.20150011010.1002/aenm.201500110 ↗
51. 10.1016/S0895-7177(01)00134-010.1016/S0895-7177(01)00134-0 ↗
52. Zintl E. · Z. Elektrochem. Angew. Phys. Chem. · 1934 · 40 · 588
53. Oftedal I. · Z. Phys. Chem‐Stoch Ve · 1927 · 128 · 15410.1515/zpch-1927-12810 ↗
54. 10.1039/C5TA04289E10.1039/C5TA04289E ↗
55. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
56. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
57. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
58. 10.1103/PhysRevB.44.1329810.1103/PhysRevB.44.13298 ↗
59. 10.1039/C4CP04532G10.1039/C4CP04532G ↗