Zinc Complex-Based Multifunctional Reactive Lithium Polysulfide Trapper Approaching Its Theoretical Efficiency
Source abstract
Abstract
The “shuttle effect” of soluble lithium polysulfides (LPS), which causes rapid capacity fading, remains a lingering issue for lithium–sulfur batteries (LSBs). Herein, we report a new type of reactive molecule-based LPS trapper, zinc acetate–diethanolamine (Zn(OAc)2·DEA), which demonstrates a molecular efficiency of 1.8 for LPS trapping, approaching its theoretical limit of 2, which is the highest trapping capability reported so far. Furthermore, the catalytic effect of Zn2+·DEA on the redox of sulfur species promotes the thermodynamics for the reduction of trapped LPS and decreases the energy barrier for the oxidation of Zn(SLi)2·DEA formed in the discharging process. LSBs using Zn(OAc)2·DEA as the LPS trapper, binder, and redox catalyst exhibited excellent long-term cycling stability (with a capacity retention of 85% after 1000 cycles at a rate of 0.5C) and enhanced rate performance. This work demonstrated the potential of this novel type of multifunctional metal complex-based reactive molecular LPS trapper for high-capacity and stable LSBs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering and Waterloo Institute for Nanotechnology (WIN), University of Waterloo, 200 University Avenue West, Waterloo, Ontario N2L 3G1, Canada
State Key Laboratory of Clean and Efficient Coal Utilization, Taiyuan University of Technology, Taiyuan 030024, Shanxi, P. R. China
Funding
Natural Sciences and Engineering Research Council of Canada · National Natural Science Foundation of China · Scientific and Technological Key Project of Shanxi Province
References (45)
Show source-provided references
1. 10.1038/nmat319110.1038/nmat3191 ↗
2. 10.1039/C5EE00838G10.1039/C5EE00838G ↗
3. 10.1002/advs.20200221210.1002/advs.202002212 ↗
4. 10.1038/nmat246010.1038/nmat2460 ↗
5. 10.1021/cr500062v10.1021/cr500062v ↗
6. 10.1126/sciadv.aay275710.1126/sciadv.aay2757 ↗
7. 10.1016/j.mattod.2018.04.00710.1016/j.mattod.2018.04.007 ↗
8. 10.1149/1.180639410.1149/1.1806394 ↗
9. 10.1002/anie.20190605510.1002/anie.201906055 ↗
10. 10.1039/C8SE00167G10.1039/C8SE00167G ↗
11. 10.1002/aenm.20190269510.1002/aenm.201902695 ↗
12. 10.1021/acs.jpcc.8b0607710.1021/acs.jpcc.8b06077 ↗
13. 10.1039/D0EE03181J10.1039/D0EE03181J ↗
14. 10.1002/cssc.20120010110.1002/cssc.201200101 ↗
15. 10.1021/ja206955k10.1021/ja206955k ↗
16. 10.1021/am501627f10.1021/am501627f ↗
17. 10.1002/adfm.20170759710.1002/adfm.201707597 ↗
18. 10.1039/C8TA04450C10.1039/C8TA04450C ↗
19. 10.1038/ncomms1120310.1038/ncomms11203 ↗
20. 10.1073/pnas.161583711410.1073/pnas.1615837114 ↗
21. 10.1002/adma.20160138210.1002/adma.201601382 ↗
22. 10.1002/adfm.20160370410.1002/adfm.201603704 ↗
23. 10.1039/C8TA07220E10.1039/C8TA07220E ↗
24. 10.1021/nl404721h10.1021/nl404721h ↗
25. 10.1002/anie.20141017410.1002/anie.201410174 ↗
26. 10.1016/j.ensm.2018.01.02010.1016/j.ensm.2018.01.020 ↗
27. 10.1021/acs.nanolett.9b0471910.1021/acs.nanolett.9b04719 ↗
28. 10.1002/anie.20200365410.1002/anie.202003654 ↗
29. 10.1002/advs.20190316810.1002/advs.201903168 ↗
30. 10.1103/PhysRevB.46.667110.1103/PhysRevB.46.6671 ↗
31. 10.1524/zkri.220.5.567.6507510.1524/zkri.220.5.567.65075 ↗
32. 10.1103/PhysRevB.41.122710.1103/PhysRevB.41.1227 ↗
33. 10.1007/s10971-018-4768-x10.1007/s10971-018-4768-x ↗
34. 10.1002/aenm.20170313810.1002/aenm.201703138 ↗
35. 10.1002/aenm.20180210710.1002/aenm.201802107 ↗
36. 10.1039/C9EE01338E10.1039/C9EE01338E ↗
37. 10.1021/jacs.8b1297310.1021/jacs.8b12973 ↗
38. 10.1002/adma.20190122010.1002/adma.201901220 ↗
39. 10.1038/ncomms668210.1038/ncomms6682 ↗
40. 10.1038/s41467-019-12542-610.1038/s41467-019-12542-6 ↗
41. 10.1002/aenm.20170007410.1002/aenm.201700074 ↗
42. 10.1039/C5EE02837J10.1039/C5EE02837J ↗
43. 10.1515/adms-2017-004210.1515/adms-2017-0042 ↗
44. 10.1039/C5EE01388G10.1039/C5EE01388G ↗
45. 10.1021/acsami.0c0956710.1021/acsami.0c09567 ↗