Transition‐Metal Oxynitride: A Facile Strategy for Improving Electrochemical Capacitor Storage
Source abstract
Abstract
Abstract The use of transition‐metal oxide (TMO) as an extended‐life electrochemical energy storage material remains challenging because TMO undergoes volume expansion during energy storage. In this work, a transition‐metal oxynitride layer (TMON, M: Fe, Co, Ni, and V) was synthesized on TMO nanowires to address the crucial issue of volume expansion. The unique oxynitride layer possesses numerous active sites, excellent conductivity, and outstanding stability. These characteristics enhance specific capacitance and alleviate volume expansion effectively. Specifically, the specific capacity of the TMON electrode is enhanced by approximately twofold relative to that of its corresponding oxide. Notably, the capacitance of the TMON remains above 94% even after 10 000 cycles. This result indicates that the cycling performance of the TMON electrode is superior to that of its corresponding oxide. First‐principles and quantitative kinetics analyses are performed to investigate the mechanism underlying the improved electrochemical performances of the TMON layers. Results demonstrate that the proposed TMON layer has attractive applications in the fields of energy storage, conversion, and beyond.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Advanced battery technologies research · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Lab of Crystal Materials Shandong University Jinan 250100 P. R. China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Shandong Province
References (54)
Show source-provided references
1. 10.1126/science.124962510.1126/science.1249625 ↗
2. 10.1002/adma.20160072510.1002/adma.201600725 ↗
3. 10.1021/acsnano.8b0191410.1021/acsnano.8b01914 ↗
4. 10.1002/aenm.20140050010.1002/aenm.201400500 ↗
5. 10.1021/nn301454q10.1021/nn301454q ↗
6. 10.1021/nl400378j10.1021/nl400378j ↗
7. 10.1039/C8TA04182B10.1039/C8TA04182B ↗
8. 10.1016/j.nanoen.2014.08.01810.1016/j.nanoen.2014.08.018 ↗
9. 10.1002/adma.20170365710.1002/adma.201703657 ↗
10. 10.1039/c0ee00669f10.1039/c0ee00669f ↗
11. 10.1021/nl400378j10.1021/nl400378j ↗
12. 10.1021/acsnano.7b0613310.1021/acsnano.7b06133 ↗
13. 10.1002/aenm.20170168110.1002/aenm.201701681 ↗
14. 10.1039/c3ee41006d10.1039/c3ee41006d ↗
15. 10.1093/nsr/nww07210.1093/nsr/nww072 ↗
16. 10.1039/C4TA05565A10.1039/C4TA05565A ↗
17. 10.1021/cm97039310.1021/cm970393 ↗
18. 10.1002/anie.20130319710.1002/anie.201303197 ↗
19. 10.1039/C7TA02704D10.1039/C7TA02704D ↗
20. 10.1039/C5MH00046G10.1039/C5MH00046G ↗
21. 10.1021/ja01379a00610.1021/ja01379a006 ↗
22. 10.1002/adfm.20130344210.1002/adfm.201303442 ↗
23. 10.1002/aenm.20180068510.1002/aenm.201800685 ↗
24. 10.1021/acsnano.8b0016810.1021/acsnano.8b00168 ↗
25. 10.1021/acsnano.7b0227510.1021/acsnano.7b02275 ↗
26. 10.1002/smtd.20170030410.1002/smtd.201700304 ↗
27. 10.1021/acsnano.7b0379410.1021/acsnano.7b03794 ↗
28. 10.1021/acsami.5b0976610.1021/acsami.5b09766 ↗
29. 10.1039/c1jm11014d10.1039/c1jm11014d ↗
30. 10.1021/jacs.6b0504610.1021/jacs.6b05046 ↗
31. 10.1039/C5TA03830H10.1039/C5TA03830H ↗
32. 10.1021/acsnano.7b0194510.1021/acsnano.7b01945 ↗
33. 10.1021/acsnano.8b0090110.1021/acsnano.8b00901 ↗
34. 10.1002/adfm.20130420610.1002/adfm.201304206 ↗
35. 10.1021/nl400760a10.1021/nl400760a ↗
36. 10.1002/smll.20160333010.1002/smll.201603330 ↗
37. 10.1039/C5TA06751K10.1039/C5TA06751K ↗
38. 10.1002/chem.20160546510.1002/chem.201605465 ↗
39. 10.1002/adma.20160416410.1002/adma.201604164 ↗
40. 10.1002/adma.20050247110.1002/adma.200502471 ↗
41. 10.1021/nl504764m10.1021/nl504764m ↗
42. 10.1038/nmat360110.1038/nmat3601 ↗
43. 10.1038/ncomms1212210.1038/ncomms12122 ↗
44. 10.1039/C5CS00580A10.1039/C5CS00580A ↗
45. 10.1039/C6TA01734G10.1039/C6TA01734G ↗
46. 10.1038/nmat481010.1038/nmat4810 ↗
47. 10.1021/acsnano.8b0148810.1021/acsnano.8b01488 ↗
48. 10.1021/jacs.7b0021610.1021/jacs.7b00216 ↗
49. 10.1021/ct500770m10.1021/ct500770m ↗
50. 10.1002/anie.20161091410.1002/anie.201610914 ↗
51. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
52. 10.1063/1.488373710.1063/1.4883737 ↗
53. 10.1063/1.156406010.1063/1.1564060 ↗
54. 10.1103/PhysRevB.96.11511810.1103/PhysRevB.96.115118 ↗