Enhancing the Lithium Storage Performance of Phosphorus–Carbon Composites by Reinforcing P–C Bonding with High-Strength Metal Nanoparticles
Source abstract
Abstract
Phosphorus is an ideal anode material for high-rate lithium-ion batteries due to its high theoretical specific capacity and moderate operating potential. However, phosphorus undergoes tremendous volume expansion and low electrical conductivity during lithium storage, affecting its actual lithium storage performance. The formation of P–C bonds is an effective strategy to inhibit the volume expansion and maintain stable electrical contact between phosphorus and the current collector. Herein, high strength metal nanoparticles, such as molybdenum nanoparticles, are introduced into the ball milling process to reinforce P–C bonding and enhance the lithium storage performance. As a result, the BP/Mo/CNTs anode provides a high-rate capacity of 984 mAh g –1 at 8.0 A g –1 and high capacity retention of 90.3% after 300 cycles at 0.5 A g –1 . To demonstrate the universality of this method, BP/W/CNTs nanocomposites were prepared by tungsten-assisted ball milling. This facile strategy provides a practical approach for the formation of abundant covalent bonds to improve the electrochemical performance of composites.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · MXene and MAX Phase Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Shenzhen Institute of Advanced Technology
Chinese Academy of Sciences
University of Chinese Academy of Sciences
Funding
China Association for Science and Technology · Youth Innovation Promotion Association of the Chinese Academy of Sciences · Natural Science Foundation of Guangdong Province
References (41)
Show source-provided references
1. 10.1002/adma.20060259210.1002/adma.200602592 ↗
2. 10.1021/acs.chemrev.3c0064610.1021/acs.chemrev.3c00646 ↗
3. 10.1039/D2CS01018F10.1039/D2CS01018F ↗
4. 10.1021/nl501617j10.1021/nl501617j ↗
5. 10.1016/j.ensm.2021.02.03010.1016/j.ensm.2021.02.030 ↗
6. 10.1021/acs.nanolett.5b0390310.1021/acs.nanolett.5b03903 ↗
7. 10.1021/acsnano.0c1037010.1021/acsnano.0c10370 ↗
8. 10.1002/adma.20220289210.1002/adma.202202892 ↗
9. 10.1016/j.joule.2019.01.01710.1016/j.joule.2019.01.017 ↗
10. 10.1016/j.ensm.2018.01.01410.1016/j.ensm.2018.01.014 ↗
11. 10.1002/adfm.20190937210.1002/adfm.201909372 ↗
12. 10.1002/adma.20230531710.1002/adma.202305317 ↗
13. 10.1002/smll.20190714110.1002/smll.201907141 ↗
14. 10.1002/aenm.20210388810.1002/aenm.202103888 ↗
15. 10.1002/adma.20210125910.1002/adma.202101259 ↗
16. 10.1002/adma.20220851410.1002/adma.202208514 ↗
17. 10.1016/j.nanoen.2019.02.06110.1016/j.nanoen.2019.02.061 ↗
18. 10.1126/science.aav584210.1126/science.aav5842 ↗
19. 10.1007/s12274-016-1383-410.1007/s12274-016-1383-4 ↗
20. 10.1002/adma.20240296110.1002/adma.202402961 ↗
21. 10.1016/j.ensm.2023.10299610.1016/j.ensm.2023.102996 ↗
22. 10.1002/smtd.20240107210.1002/smtd.202401072 ↗
23. 10.1016/j.ensm.2022.02.05310.1016/j.ensm.2022.02.053 ↗
24. 10.1039/D4EE00970C10.1039/D4EE00970C ↗
25. 10.1021/jacs.4c0369110.1021/jacs.4c03691 ↗
26. 10.1002/aenm.20230440810.1002/aenm.202304408 ↗
27. 10.1016/j.jechem.2022.02.03510.1016/j.jechem.2022.02.035 ↗
28. 10.1016/j.jpowsour.2023.23365010.1016/j.jpowsour.2023.233650 ↗
29. 10.1002/ente.20230038710.1002/ente.202300387 ↗
30. 10.1002/adma.20230361010.1002/adma.202303610 ↗
31. 10.1021/acs.nanolett.2c0303810.1021/acs.nanolett.2c03038 ↗
32. 10.1016/j.ensm.2019.12.04410.1016/j.ensm.2019.12.044 ↗
33. 10.1039/D0CC01853H10.1039/D0CC01853H ↗
34. 10.1002/adfm.20230832510.1002/adfm.202308325 ↗
35. 10.1002/anie.20191312910.1002/anie.201913129 ↗
36. 10.1002/smll.20240248310.1002/smll.202402483 ↗
37. 10.1016/j.ensm.2022.05.05610.1016/j.ensm.2022.05.056 ↗
38. 10.1016/j.cej.2024.15101210.1016/j.cej.2024.151012 ↗
39. 10.1021/acs.nanolett.3c0065610.1021/acs.nanolett.3c00656 ↗
40. 10.1016/j.chempr.2022.05.00210.1016/j.chempr.2022.05.002 ↗
41. 10.1002/adma.20210965810.1002/adma.202109658 ↗