journal article·2019-04

Empowering Metal Phosphides Anode with Catalytic Attribute toward Superior Cyclability for Lithium‐Ion Storage

Huadong Yuan, Min Wu, Jianhui Zheng, Zhi‐Gang Chen, Wenkui Zhang, Jianmin Luo, Chengbin Jin, Ouwei Sheng, Chu Liang, Yongping Gan, Yang Xia, Jun Zhang, Hui Huang, Yujing Liu, Jianwei Nai, Xinyong Tao

Advanced Functional Materials· Volume 29· Issue 17
Publisher page

Abstract

Abstract Due to high capacity, moderate redox voltage, and relatively low polarization, metal phosphides (MPs) attract much attention as viable anode materials for lithium‐ion storage. However, severe capacity decay induced by the poor reversibility of discharge product (Li3P) in these anodes suppresses their practical applications. Herein, it is first revealed that N‐doped carbon can effectively catalyze the oxidation of Li3P by density functional theory calculations and activation experiments. By anchoring Ni2P nanoparticles on N‐doped carbon sheets (Ni2P@N‐C) via a facile method, an MP‐based anode rendered with a catalytic attribute is successfully fabricated for improving the reversibility of Li3P during lithium‐ion storage. Benefiting from this design, not only can high capacity and rate performance be reached, but also an extraordinary cyclability and capacity retention be realized, which is the best among all other phosphides reported so far. By employing such a Ni2P@N‐C composite and a commercialized active carbon as the anode and cathode, respectively, hybrid lithium‐ion capacitors can be fabricated with an ultrahigh energy density of 80 Wh kg−1 at a power density of 12.5 kW kg−1. This strategy of designing electrodes may be generalized to other energy storage systems whose cycling performance needs to be improved.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · Supercapacitor Materials and Fabrication · Advanced Battery Materials and Technologies

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

Affiliations

College of Materials Science and Engineering Zhejiang University of Technology Hangzhou 310014 China

Centre for Future Materials University of Southern Queensland Springfield Queensland 4300 Australia

Funding

National Natural Science Foundation of China · Natural Science Foundation of Zhejiang Province

References (71)

Show source-provided references
1. 10.1126/science.121300310.1126/science.1213003 ↗
2. 10.1038/nmat483410.1038/nmat4834 ↗
3. 10.1038/nmat229710.1038/nmat2297 ↗
4. 10.1021/cr500091510.1021/cr5000915 ↗
5. 10.1002/adma.20170209310.1002/adma.201702093 ↗
6. 10.1002/aenm.20170066810.1002/aenm.201700668 ↗
7. 10.1021/nl400600x10.1021/nl400600x ↗
8. 10.1021/acsnano.6b0047910.1021/acsnano.6b00479 ↗
9. 10.1002/adfm.20110005810.1002/adfm.201100058 ↗
10. 10.1126/science.124962510.1126/science.1249625 ↗
11. 10.1039/c3ee40509e10.1039/c3ee40509e ↗
12. 10.1002/adfm.20140239810.1002/adfm.201402398 ↗
13. 10.1002/adma.20170014210.1002/adma.201700142 ↗
14. 10.1002/adma.20150162210.1002/adma.201501622 ↗
15. 10.1002/aenm.20150095910.1002/aenm.201500959 ↗
16. 10.1002/aenm.20130046710.1002/aenm.201300467 ↗
17. 10.1021/acsnano.7b0917510.1021/acsnano.7b09175 ↗
18. 10.1002/adfm.20170433010.1002/adfm.201704330 ↗
19. 10.1002/smll.20140262010.1002/smll.201402620 ↗
20. 10.1021/acsnano.6b0766810.1021/acsnano.6b07668 ↗
21. 10.1021/acsnano.6b0822310.1021/acsnano.6b08223 ↗
22. 10.1016/j.ensm.2017.07.01310.1016/j.ensm.2017.07.013 ↗
23. 10.1002/adfm.20140447210.1002/adfm.201404472 ↗
24. 10.1002/aenm.20150055010.1002/aenm.201500550 ↗
25. 10.1021/acs.nanolett.8b0013410.1021/acs.nanolett.8b00134 ↗
26. 10.1002/adfm.20130313810.1002/adfm.201303138 ↗
27. 10.1002/aenm.20170122210.1002/aenm.201701222 ↗
28. 10.1039/C5EE03149D10.1039/C5EE03149D ↗
29. 10.1002/adfm.20150524010.1002/adfm.201505240 ↗
30. 10.1016/j.nanoen.2018.03.05310.1016/j.nanoen.2018.03.053 ↗
31. 10.1002/adma.20160401510.1002/adma.201604015 ↗
32. 10.1002/adfm.20110266010.1002/adfm.201102660 ↗
33. 10.1016/j.ensm.2018.04.01110.1016/j.ensm.2018.04.011 ↗
34. 10.1021/jacs.5b0452610.1021/jacs.5b04526 ↗
35. 10.1002/aenm.20170133610.1002/aenm.201701336 ↗
36. 10.1016/S1388-2481(02)00363-610.1016/S1388-2481(02)00363-6 ↗
37. 10.1002/adma.20130560810.1002/adma.201305608 ↗
38. 10.12677/NAT.2014.4100110.12677/NAT.2014.41001 ↗
39. 10.1002/adma.20170274710.1002/adma.201702747 ↗
40. 10.1002/adma.20150619710.1002/adma.201506197 ↗
41. 10.1002/aenm.20150149210.1002/aenm.201501492 ↗
42. 10.1021/ja305220610.1021/ja3052206 ↗
43. 10.1021/acs.nanolett.6b0293210.1021/acs.nanolett.6b02932 ↗
44. 10.1021/acsnano.6b0770710.1021/acsnano.6b07707 ↗
45. Lu Y. · J. Mater. Chem. C · 2012 · 116 · 22217
46. 10.1021/jp208204u10.1021/jp208204u ↗
47. 10.1016/j.nanoen.2018.04.00110.1016/j.nanoen.2018.04.001 ↗
48. 10.1039/C5TA01103E10.1039/C5TA01103E ↗
49. 10.1021/acsomega.8b0048210.1021/acsomega.8b00482 ↗
50. 10.1039/C6TA06705K10.1039/C6TA06705K ↗
51. 10.1039/C8QI00243F10.1039/C8QI00243F ↗
52. 10.1039/C7TA08386F10.1039/C7TA08386F ↗
53. 10.1039/C7TA00139H10.1039/C7TA00139H ↗
54. 10.1039/C5NR05432J10.1039/C5NR05432J ↗
55. 10.1039/C4NR05862C10.1039/C4NR05862C ↗
56. 10.1002/aenm.20170213410.1002/aenm.201702134 ↗
57. 10.1002/adma.20180231010.1002/adma.201802310 ↗
58. 10.1021/acsnano.7b0662510.1021/acsnano.7b06625 ↗
59. 10.1021/acsami.8b1046210.1021/acsami.8b10462 ↗
60. 10.1021/acsami.7b0282610.1021/acsami.7b02826 ↗
61. 10.1021/acs.iecr.8b0203610.1021/acs.iecr.8b02036 ↗
62. 10.1002/adma.20170567010.1002/adma.201705670 ↗
63. 10.1016/j.nanoen.2016.07.01810.1016/j.nanoen.2016.07.018 ↗
64. 10.1002/adfm.20180275610.1002/adfm.201802756 ↗
65. 10.1002/smll.20177018710.1002/smll.201770187 ↗
66. 10.1016/j.ensm.2018.05.02010.1016/j.ensm.2018.05.020 ↗
67. 10.1002/aenm.20170289510.1002/aenm.201702895 ↗
68. 10.1021/nn501972w10.1021/nn501972w ↗
69. 10.1149/2.003208jes10.1149/2.003208jes ↗
70. 10.1002/adfm.20120076610.1002/adfm.201200766 ↗
71. 10.1021/ja207285b10.1021/ja207285b ↗