Cu-Based Ternary Heterostructures for High-Performance Asymmetric Supercapacitors
Source abstract
Abstract
In view of cost, electrical conductivity, and environmental friendliness, copper-based heterostructures are suitable alternatives to toxic ruthenium-based materials in a variety of applications, such as catalysis, biological imaging, energy conversion, and storage. The primary hindrances limiting energy-storage performance are heterostructures with irregular sizes, shapes, and compositions. Here, we introduce a three-step strategy to synthesize CuS 2 @Cu 7 Se 4 @NC hollow heterostructures, starting from Cu 2 O nanocubes and proceeding through two anion exchanges and a carbon coating step. Taking advantage of the electrical synergistic effect and hollow structures, the as-synthesized CuS 2 @Cu 7 Se 4 @NC hollow heterostructures exhibit an excellent electrochemical performance when utilized as a supercapacitor electrode, achieving a high specific capacitance of 660 F g –1 at 1 A g –1 with a good rate capability and excellent cycling stability (retaining 72.6% of its initial capacitance after 4000 charge–discharge cycles). By coupling with commercially activated carbon (AC), an asymmetric supercapacitor device was constructed (CuS 2 @Cu 7 Se 4 @NC//AC) using KOH-PVA as an electrolyte, which delivers an elevated energy density at a power density of 599.7 W kg –1 and reasonable cycling stability (77.6% retention, 4000 cycles at 10 A g –1 ), suggesting a wide range of potential uses for the CuS 2 @Cu 7 Se 4 @NC electrode in supercapacitors and associated energy applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Electrocatalysts for Energy Conversion · MXene and MAX Phase Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science & Engineering, Jiangsu University, Zhenjiang 212013, P. R. China
Funding
Government of Jiangsu Province
References (61)
Show source-provided references
1. 10.1021/acsnano.3c0938610.1021/acsnano.3c09386 ↗
2. 10.1021/acsnano.7b0279610.1021/acsnano.7b02796 ↗
3. 10.1002/aoc.730110.1002/aoc.7301 ↗
4. 10.1002/adma.20160533610.1002/adma.201605336 ↗
5. 10.1039/D3SE00565H10.1039/D3SE00565H ↗
6. 10.1016/j.jpowsour.2020.22914310.1016/j.jpowsour.2020.229143 ↗
7. 10.1039/D3GC03525E10.1039/D3GC03525E ↗
8. 10.1002/cnma.20220053710.1002/cnma.202200537 ↗
9. 10.1016/j.est.2022.10407310.1016/j.est.2022.104073 ↗
10. 10.1016/j.cej.2023.14174510.1016/j.cej.2023.141745 ↗
11. 10.1016/j.gee.2022.07.00210.1016/j.gee.2022.07.002 ↗
12. 10.1002/aoc.753310.1002/aoc.7533 ↗
13. 10.1016/j.cej.2021.13274510.1016/j.cej.2021.132745 ↗
14. 10.3390/nano1401002210.3390/nano14010022 ↗
15. 10.1002/cssc.20190176610.1002/cssc.201901766 ↗
16. 10.1002/smll.20220024810.1002/smll.202200248 ↗
17. 10.1016/j.jechem.2017.03.00710.1016/j.jechem.2017.03.007 ↗
18. 10.1016/j.est.2023.10844710.1016/j.est.2023.108447 ↗
19. 10.1016/j.cej.2021.13153510.1016/j.cej.2021.131535 ↗
20. 10.1016/j.chemosphere.2023.13972010.1016/j.chemosphere.2023.139720 ↗
21. 10.1021/acsaem.8b0162710.1021/acsaem.8b01627 ↗
22. 10.1021/acsami.1c0910710.1021/acsami.1c09107 ↗
23. 10.1021/acs.energyfuels.3c0355110.1021/acs.energyfuels.3c03551 ↗
24. 10.1021/acsaem.3c0091710.1021/acsaem.3c00917 ↗
25. 10.1021/acs.langmuir.3c0062710.1021/acs.langmuir.3c00627 ↗
26. 10.1016/j.apsusc.2022.15613210.1016/j.apsusc.2022.156132 ↗
27. 10.1016/j.cej.2023.14459010.1016/j.cej.2023.144590 ↗
28. 10.1016/j.cej.2023.14821310.1016/j.cej.2023.148213 ↗
29. 10.1039/D3GC03080F10.1039/D3GC03080F ↗
30. 10.1016/j.cej.2022.13654010.1016/j.cej.2022.136540 ↗
31. 10.1021/cm801407q10.1021/cm801407q ↗
32. 10.1021/acsami.1c2098010.1021/acsami.1c20980 ↗
33. 10.1021/ic900201p10.1021/ic900201p ↗
34. 10.1021/cg101283w10.1021/cg101283w ↗
35. 10.1021/la904292t10.1021/la904292t ↗
36. 10.1021/cm303092810.1021/cm3030928 ↗
37. 10.1021/acs.nanolett.5b0284210.1021/acs.nanolett.5b02842 ↗
38. 10.1021/acsami.5b1027810.1021/acsami.5b10278 ↗
39. 10.1021/acsami.9b0532510.1021/acsami.9b05325 ↗
40. 10.1021/acsanm.1c0293610.1021/acsanm.1c02936 ↗
41. 10.1021/acsami.8b1810710.1021/acsami.8b18107 ↗
42. 10.1016/j.electacta.2019.06.01110.1016/j.electacta.2019.06.011 ↗
43. 10.1021/acsaelm.3c0015210.1021/acsaelm.3c00152 ↗
44. 10.1002/eom2.1228310.1002/eom2.12283 ↗
45. 10.1039/D1TA09264B10.1039/D1TA09264B ↗
46. 10.1016/j.carbon.2020.04.08410.1016/j.carbon.2020.04.084 ↗
47. 10.1002/smll.20170257010.1002/smll.201702570 ↗
48. 10.1016/j.jpowsour.2022.23107210.1016/j.jpowsour.2022.231072 ↗
49. 10.1016/j.jelechem.2022.11661010.1016/j.jelechem.2022.116610 ↗
50. 10.1016/j.matlet.2017.03.10810.1016/j.matlet.2017.03.108 ↗
51. 10.1016/j.tsf.2019.13758410.1016/j.tsf.2019.137584 ↗
52. 10.1016/j.jallcom.2020.15746610.1016/j.jallcom.2020.157466 ↗
53. 10.1007/s11051-019-4660-910.1007/s11051-019-4660-9 ↗
54. 10.1021/acs.inorgchem.3c0030810.1021/acs.inorgchem.3c00308 ↗
55. 10.1016/j.apsusc.2017.12.19910.1016/j.apsusc.2017.12.199 ↗
56. 10.1016/j.solidstatesciences.2020.10633610.1016/j.solidstatesciences.2020.106336 ↗
57. 10.1016/j.est.2021.10330810.1016/j.est.2021.103308 ↗
58. 10.1016/j.est.2022.10530410.1016/j.est.2022.105304 ↗
59. 10.1039/D2QM00450J10.1039/D2QM00450J ↗
60. 10.1016/j.jallcom.2021.16278410.1016/j.jallcom.2021.162784 ↗
61. 10.1016/j.cej.2021.12892410.1016/j.cej.2021.128924 ↗