journal article·2023-10-04

MoO2/t-C3N4 Heterogeneous Materials with Bidirectional Catalysis for the Rapid Conversion of S Species in Li–S Batteries

Yongqian He, Yixin Luo, Wanqi Zhang, Sisi Liu, Kai Zhu, Li Huang, Yue Yang, Xin Li, Ruizhi Yu, Hongbo Shu, Xianyou Wang, Manfang Chen

ACS Applied Materials & Interfaces· Volume 15· Issue 39
Publisher page

Abstract

Li–S batteries have drawn a lot of attention for their high theoretical specific capacity and significant economic benefits. However, the shuttle effect of polysulfides prevents them from being used widely. To tackle this difficulty, a heterogeneous structure based on tubular carbon nitride with evenly dispersed molybdenum dioxide nanoparticles (MoO 2 /t-C 3 N 4 ) as the S host is constructed in this work. As a polar material with a large specific surface area, MoO 2 /t-C 3 N 4 has a strong anchoring effect on polysulfide. Additionally, the heterogeneous material has excellent bidirectional catalytic ability for the redox process of S species based on the action of the built-in electric field formed by electron directional transfer. Not only does it improve the reaction kinetics of the redox process of the polysulfides but it also prevents polysulfides from accumulating on the surface of the modified material and deactivating it, further improving the utilization of the active material. Thus, MoO 2 /t-C 3 N 4 /S shows the high initial-discharge specific capacity of 812.7 mAh g –1 at the current density of 5C, and the Coulombic efficiency is maintained at more than 95% after 400 charge/discharge cycles. Moreover, MoO 2 /t-C 3 N 4 /S achieved a capacity retention of 89% after 100 cycles at the current density of 0.1C under the high S loading. Therefore, the research results of this work provide a trustworthy reference for the future commercial application of Li–S batteries.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · MXene and MAX Phase Materials

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

Affiliations

National Base for International Science & Technology Cooperation, School of Chemistry, Xiangtan University, Xiangtan 411105, China

Institute of Micro/Nano Materials and Devices, Ningbo University of Technology, Ningbo 315211, P.R. China

Funding

Natural Science Foundation of??Hunan Province · China Postdoctoral Science Foundation · National Natural Science Foundation of China

References (56)

Show source-provided references
1. 10.1016/j.joule.2019.01.00310.1016/j.joule.2019.01.003 ↗
2. 10.1002/inf2.1236110.1002/inf2.12361 ↗
3. 10.1002/eom2.1218210.1002/eom2.12182 ↗
4. 10.1016/j.gee.2022.03.00610.1016/j.gee.2022.03.006 ↗
5. 10.1016/j.nantod.2018.02.00610.1016/j.nantod.2018.02.006 ↗
6. 10.1016/j.carbon.2020.01.04610.1016/j.carbon.2020.01.046 ↗
7. 10.1002/adma.20230077110.1002/adma.202300771 ↗
8. 10.1002/adma.20221211610.1002/adma.202212116 ↗
9. 10.1002/adma.20230352010.1002/adma.202303520 ↗
10. 10.1002/aenm.20220354010.1002/aenm.202203540 ↗
11. 10.1002/aenm.20220158510.1002/aenm.202201585 ↗
12. 10.1016/j.nanoen.2015.05.00610.1016/j.nanoen.2015.05.006 ↗
13. 10.1016/j.nanoen.2015.01.03310.1016/j.nanoen.2015.01.033 ↗
14. 10.1021/nn404439r10.1021/nn404439r ↗
15. 10.1016/j.nanoen.2018.06.04410.1016/j.nanoen.2018.06.044 ↗
16. 10.1002/adfm.20210716610.1002/adfm.202107166 ↗
17. 10.1016/j.nanoen.2022.10779410.1016/j.nanoen.2022.107794 ↗
18. 10.1016/j.apcatb.2017.06.00310.1016/j.apcatb.2017.06.003 ↗
19. 10.1016/j.electacta.2016.06.03210.1016/j.electacta.2016.06.032 ↗
20. 10.1002/batt.20180004010.1002/batt.201800040 ↗
21. 10.1016/j.cej.2019.12390510.1016/j.cej.2019.123905 ↗
22. 10.1002/solr.20190041610.1002/solr.201900416 ↗
23. 10.1021/nn800844h10.1021/nn800844h ↗
24. 10.1021/acsami.8b1517610.1021/acsami.8b15176 ↗
25. 10.1063/1.512722710.1063/1.5127227 ↗
26. 10.1002/aenm.20210043210.1002/aenm.202100432 ↗
27. 10.1016/j.jechem.2023.04.01610.1016/j.jechem.2023.04.016 ↗
28. 10.1002/smll.20230006510.1002/smll.202300065 ↗
29. 10.1039/c3ta14576j10.1039/c3ta14576j ↗
30. 10.1002/adfm.20110230610.1002/adfm.201102306 ↗
31. 10.1016/j.cej.2020.12817710.1016/j.cej.2020.128177 ↗
32. 10.1016/j.jpowsour.2019.05.04510.1016/j.jpowsour.2019.05.045 ↗
33. 10.1016/j.matlet.2017.11.04710.1016/j.matlet.2017.11.047 ↗
34. 10.1016/j.jphotochemrev.2014.04.00210.1016/j.jphotochemrev.2014.04.002 ↗
35. 10.1016/j.ceramint.2015.10.00810.1016/j.ceramint.2015.10.008 ↗
36. 10.1002/smll.20220694010.1002/smll.202206940 ↗
37. 10.1039/C7TA08859K10.1039/C7TA08859K ↗
38. 10.1016/j.jmst.2021.10.04410.1016/j.jmst.2021.10.044 ↗
39. 10.1016/j.ensm.2017.07.01510.1016/j.ensm.2017.07.015 ↗
40. 10.1021/acsaem.1c0214810.1021/acsaem.1c02148 ↗
41. 10.1016/j.apsusc.2021.15098410.1016/j.apsusc.2021.150984 ↗
42. 10.1021/acsanm.2c0312410.1021/acsanm.2c03124 ↗
43. 10.1021/acsami.3c0738210.1021/acsami.3c07382 ↗
44. 10.1021/acsami.1c0406910.1021/acsami.1c04069 ↗
45. 10.1016/j.jpowsour.2019.05.05510.1016/j.jpowsour.2019.05.055 ↗
46. 10.1002/smll.20220608310.1002/smll.202206083 ↗
47. 10.1002/aenm.20220223210.1002/aenm.202202232 ↗
48. 10.1038/s41929-023-00912-910.1038/s41929-023-00912-9 ↗
49. 10.1002/advs.20160010110.1002/advs.201600101 ↗
50. 10.1002/advs.20220402710.1002/advs.202204027 ↗
51. 10.1021/acsami.0c1663110.1021/acsami.0c16631 ↗
52. 10.1016/j.jechem.2018.02.01010.1016/j.jechem.2018.02.010 ↗
53. 10.1016/j.jechem.2019.01.01910.1016/j.jechem.2019.01.019 ↗
54. 10.1016/j.jechem.2020.05.03610.1016/j.jechem.2020.05.036 ↗
55. Liu Y. · Adv. Funct. Mater. · 2022 · 32 · 210946210.1002/adfm.202109462 ↗
56. 10.1002/adfm.20221181810.1002/adfm.202211818 ↗