Spontaneous Growth of 3D Framework Carbon from Sodium Citrate for High Energy‐ and Power‐Density and Long‐Life Sodium‐Ion Hybrid Capacitors
Source abstract
Abstract
Abstract Carbon sheets with 3D architectures, large graphitic interlayer spacing, and high electrical conductivity are highly expected to be an ideal anode material for sodium‐ion hybrid capacitors (SIHCs). Pursuing a simple synthesis methodology and advancing it from the laboratory to industry is of great importance. In this study, a new approach is presented to prepare 3D framework carbon (3DFC) with the above integrated advantages by a direct calcination of sodium citrate without aid of any additional carbon source, template, or catalyst. The first‐principle calculations verify that the large interlayer spacing and the curvature structure of 3DFC facilitate the sodium ion insertion/extraction. As a consequence, the optimal 3DFC sample exhibits high reversible capacity as well as excellent rate and cycling performance. On this basis, a dual‐carbon SIHC is fabricated by employing 3DFC as battery‐type anode and 3DFC‐derived nanoporous carbon as capacitor‐type cathode. It is able to deliver high energy‐ and power‐density feature as well as outstanding long‐term cycling stability in the potential range of 0–4.0 V. This study may open an avenue for developing high‐performance carbon electrode materials and pushes the practical applications of SIHCs a decisive step forward.
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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
Laboratory of Clean Energy Chemistry and Materials State Key Laboratory of Solid Lubrication Lanzhou Institute of Chemical Physics Chinese Academy of Sciences Lanzhou 730000 P. R. China
University of Chinese Academy of Sciences Beijing 100039 P. R. China
School of Materials Science and Engineering Shanghai University Shanghai 200444 P. R. China
Funding
National Natural Science Foundation of China
References (66)
Show source-provided references
1. 10.1038/3510464410.1038/35104644 ↗
2. 10.1038/nmat319110.1038/nmat3191 ↗
3. 10.1002/aenm.20160094310.1002/aenm.201600943 ↗
4. 10.1021/acsami.6b0798910.1021/acsami.6b07989 ↗
5. 10.1038/natrevmats.2016.8010.1038/natrevmats.2016.80 ↗
6. 10.1039/C6EE02070D10.1039/C6EE02070D ↗
7. 10.1038/nmat229710.1038/nmat2297 ↗
8. 10.1039/C5CS00580A10.1039/C5CS00580A ↗
9. 10.1039/C5EE03109E10.1039/C5EE03109E ↗
10. 10.1021/ja309143810.1021/ja3091438 ↗
11. 10.1021/ja507828x10.1021/ja507828x ↗
12. 10.1021/cm901452z10.1021/cm901452z ↗
13. 10.1038/nenergy.2016.7110.1038/nenergy.2016.71 ↗
14. 10.1039/c3ee40847g10.1039/c3ee40847g ↗
15. 10.1021/acs.accounts.5b0048210.1021/acs.accounts.5b00482 ↗
16. Slater M. D. · Adv. Funct. Mater. · 2013 · 23 · 94
17. 10.1002/aenm.20150071610.1002/aenm.201500716 ↗
18. 10.1021/acs.nanolett.7b0136610.1021/acs.nanolett.7b01366 ↗
19. 10.1002/anie.20141037610.1002/anie.201410376 ↗
20. 10.1021/cr500091510.1021/cr5000915 ↗
21. 10.1038/ncomms1264710.1038/ncomms12647 ↗
22. 10.1002/adfm.20140447210.1002/adfm.201404472 ↗
23. 10.1039/C6TA02478E10.1039/C6TA02478E ↗
24. 10.1021/acs.nanolett.6b0293210.1021/acs.nanolett.6b02932 ↗
25. 10.1002/adfm.20150554810.1002/adfm.201505548 ↗
26. 10.1021/acs.jpclett.5b0086810.1021/acs.jpclett.5b00868 ↗
27. 10.1038/ncomms754410.1038/ncomms7544 ↗
28. 10.1002/aenm.20170122210.1002/aenm.201701222 ↗
29. 10.1021/nn300920e10.1021/nn300920e ↗
30. 10.1039/C2EE23284G10.1039/C2EE23284G ↗
31. 10.1002/adma.20110450210.1002/adma.201104502 ↗
32. 10.1021/ar300253f10.1021/ar300253f ↗
33. 10.1021/acs.accounts.6b0054110.1021/acs.accounts.6b00541 ↗
34. 10.1002/adfm.20160189710.1002/adfm.201601897 ↗
35. 10.1039/C5TA03706A10.1039/C5TA03706A ↗
36. 10.1002/adfm.20150372610.1002/adfm.201503726 ↗
37. 10.1038/ncomms441010.1038/ncomms4410 ↗
38. 10.1002/aenm.20160277810.1002/aenm.201602778 ↗
39. 10.1002/aenm.20110069110.1002/aenm.201100691 ↗
40. 10.1039/C3NR05374A10.1039/C3NR05374A ↗
41. 10.1021/nn404640c10.1021/nn404640c ↗
42. 10.1039/C6EE02274J10.1039/C6EE02274J ↗
43. 10.1021/am404788e10.1021/am404788e ↗
44. 10.1039/C6CC06990H10.1039/C6CC06990H ↗
45. 10.1039/C5TA01443C10.1039/C5TA01443C ↗
46. 10.1016/j.ensm.2015.10.00310.1016/j.ensm.2015.10.003 ↗
47. 10.1016/j.nanoen.2015.03.01710.1016/j.nanoen.2015.03.017 ↗
48. 10.1039/C4TA04995K10.1039/C4TA04995K ↗
49. 10.1002/adma.20150381610.1002/adma.201503816 ↗
50. 10.1002/adma.20160410810.1002/adma.201604108 ↗
51. 10.1002/jcc.2049510.1002/jcc.20495 ↗
52. 10.1002/jcc.2434210.1002/jcc.24342 ↗
53. 10.1039/C4EE02986K10.1039/C4EE02986K ↗
54. 10.1002/celc.20140235910.1002/celc.201402359 ↗
55. 10.1016/j.jpowsour.2015.08.01110.1016/j.jpowsour.2015.08.011 ↗
56. 10.1002/adma.20150309710.1002/adma.201503097 ↗
57. 10.1016/j.jpowsour.2013.05.13210.1016/j.jpowsour.2013.05.132 ↗
58. 10.1021/am300385r10.1021/am300385r ↗
59. 10.1016/j.nanoen.2016.03.01410.1016/j.nanoen.2016.03.014 ↗
60. 10.1021/acsnano.6b0833210.1021/acsnano.6b08332 ↗
61. 10.1002/aenm.20160265410.1002/aenm.201602654 ↗
62. 10.1039/C6TA01392A10.1039/C6TA01392A ↗
63. 10.1039/C7TA00463J10.1039/C7TA00463J ↗
64. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
65. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
66. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗