Ni-Doped Cobalt–Cobalt Nitride Heterostructure Arrays for High-Power Supercapacitors
Source abstract
Abstract
Metal nitrides are widely recognized as a class of desirable supercapacitor electrode materials owing to their high electrical conductivity and structural stability. Embedding metal nanoparticles in nitrides can further enhance the conductivity for electron transport. Herein, a heterostructure consisting of Ni-doped Co–Co2N is synthesized by simple thermal annealing of metal–organic framework (MOF)-derived NiCo2O4 in ammonia atmosphere, in the process of which the MOF-derived two-dimensional (2D) nanoflake arrays were well retained, and the metal–metal nitride heterostructure was well established when annealed at 350 °C. Benefiting from the MOF-derived 2D nanoflake morphology and the metal-metal nitride heterostructure, the Ni-doped Co–Co2N delivers a specific capacity of 361.93 C/g. A full cell test has been conducted using Ni-doped Co–Co2N as the positive electrode and porous carbon as the negative electrode, and it shows an energy density of 20.4 Wh/kg at the power density of 9.85 kW/kg with 82.4% of initial energy density being retained after 5000 cycles.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · MXene and MAX Phase Materials · Electrocatalysts for Energy Conversion
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, National University of Singapore, 117574 Singapore, Singapore
Department of Chemical & Biomolecular Engineering, National University of Singapore, 117585 Singapore, Singapore
Funding
Ministry of Education - Singapore
References (56)
Show source-provided references
1. 10.1039/C4RA06136E10.1039/C4RA06136E ↗
2. 10.1021/acsnano.7b0379410.1021/acsnano.7b03794 ↗
3. 10.1002/advs.20150028610.1002/advs.201500286 ↗
4. 10.1021/acsnano.6b0853410.1021/acsnano.6b08534 ↗
5. 10.1002/adfm.20140447210.1002/adfm.201404472 ↗
6. 10.1002/adma.20130146510.1002/adma.201301465 ↗
7. 10.1002/adma.20150183810.1002/adma.201501838 ↗
8. 10.1002/adma.20160072510.1002/adma.201600725 ↗
9. 10.1016/j.mattod.2017.03.01910.1016/j.mattod.2017.03.019 ↗
10. 10.1039/C4TA05565A10.1039/C4TA05565A ↗
11. 10.1039/C5CS00303B10.1039/C5CS00303B ↗
12. 10.1149/1.357402110.1149/1.3574021 ↗
13. 10.1021/nl504872s10.1021/nl504872s ↗
14. 10.1021/acs.nanolett.6b0380310.1021/acs.nanolett.6b03803 ↗
15. 10.1002/cssc.20170145610.1002/cssc.201701456 ↗
16. 10.1039/C5EE03633J10.1039/C5EE03633J ↗
17. 10.1021/acsami.5b0446310.1021/acsami.5b04463 ↗
18. 10.1021/nn503814y10.1021/nn503814y ↗
19. 10.1039/C7NR05560A10.1039/C7NR05560A ↗
20. 10.1039/C5TA03830H10.1039/C5TA03830H ↗
21. 10.1039/C6TA02492K10.1039/C6TA02492K ↗
22. 10.1039/C8RA00347E10.1039/C8RA00347E ↗
23. 10.1021/am100319u10.1021/am100319u ↗
24. 10.1016/j.electacta.2008.04.04810.1016/j.electacta.2008.04.048 ↗
25. 10.1016/j.nanoen.2014.04.01010.1016/j.nanoen.2014.04.010 ↗
26. 10.1149/1.273921210.1149/1.2739212 ↗
27. 10.1016/j.nanoen.2018.01.01510.1016/j.nanoen.2018.01.015 ↗
28. 10.1002/adma.20170551610.1002/adma.201705516 ↗
29. 10.1002/smll.20170264110.1002/smll.201702641 ↗
30. 10.1002/aenm.20160239110.1002/aenm.201602391 ↗
31. 10.1016/j.rser.2015.12.11710.1016/j.rser.2015.12.117 ↗
32. 10.1039/c3nr03829g10.1039/c3nr03829g ↗
33. 10.1002/adfm.20080048810.1002/adfm.200800488 ↗
34. 10.1038/ncomms1426410.1038/ncomms14264 ↗
35. 10.1038/ncomms293210.1038/ncomms2932 ↗
36. 10.1149/1.164998310.1149/1.1649983 ↗
37. 10.1039/C7TA10933D10.1039/C7TA10933D ↗
38. 10.1002/chem.20170059410.1002/chem.201700594 ↗
39. 10.1002/ejic.20180039210.1002/ejic.201800392 ↗
40. 10.1016/j.ensm.2018.06.00110.1016/j.ensm.2018.06.001 ↗
41. 10.1002/anie.20160437210.1002/anie.201604372 ↗
42. 10.1016/j.electacta.2015.12.17410.1016/j.electacta.2015.12.174 ↗
43. 10.2355/isijinternational.55.73610.2355/isijinternational.55.736 ↗
44. 10.1021/es102910q10.1021/es102910q ↗
45. 10.1016/j.nanoen.2013.11.00110.1016/j.nanoen.2013.11.001 ↗
46. 10.1016/j.jpowsour.2015.03.10610.1016/j.jpowsour.2015.03.106 ↗
47. 10.1002/adfm.20110283910.1002/adfm.201102839 ↗
48. 10.1016/j.electacta.2012.09.07510.1016/j.electacta.2012.09.075 ↗
49. 10.1039/C3TA15373H10.1039/C3TA15373H ↗
50. 10.1016/j.jcis.2017.08.00310.1016/j.jcis.2017.08.003 ↗
51. 10.1016/j.electacta.2015.02.09510.1016/j.electacta.2015.02.095 ↗
52. 10.1016/j.jpowsour.2016.03.03510.1016/j.jpowsour.2016.03.035 ↗
53. 10.1016/j.jpowsour.2014.01.06410.1016/j.jpowsour.2014.01.064 ↗
54. 10.1039/c2jm35307e10.1039/c2jm35307e ↗
55. 10.1016/j.electacta.2015.12.01810.1016/j.electacta.2015.12.018 ↗
56. 10.1039/c2nr31590d10.1039/c2nr31590d ↗