Fe3O4/Nitrogen‐Doped Carbon Electrodes from Tailored Thermal Expansion toward Flexible Solid‐State Asymmetric Supercapacitors
Source abstract
Abstract
Abstract Transition metal oxide and heteroatoms doped carbon are promising in high performance energy storage upon complete redox reaction. Herein, nanoparticle‐embedded carbon nanosheets are fabricated by a one‐pot tailored thermally expansion of viscous precursors. The obtained biomass carbon exhibits ideal surface area, crystal structures, and heteroatom doping. Benefiting from the synergistic effect of the constituent components, this composite electrode reaches a high potential window of 1.1 V and delivers a good specific capacitance of 522.7 F g−1 in aqueous electrolyte. After combining with a capacitive carbon nanotubes (CNTs) film cathode, the assembled flexible solid‐state supercapacitors deliver a high energy density of 18.1 Wh kg−1 at a power density of 125 W kg−1. Moreover, in cases of frequent bending and elevated temperature (up to 80 °C), the hybrid device maintains superior electrochemical attributes. This facile and scalable process, as well as their high reversible capacity, are promising for next‐generation energy‐storage devices.
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
Beijing Engineering Research Centre of Cellulose and Its Derivatives School of Materials Science and Engineering Beijing Institute of Technology Beijing 100081 China
State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University Beijing 100084 China
Funding
Natural Science Foundation of Beijing Municipality · China Postdoctoral Science Foundation
References (71)
Show source-provided references
1. 10.1126/science.aab379810.1126/science.aab3798 ↗
2. 10.1126/science.aam585210.1126/science.aam5852 ↗
3. 10.1002/admi.20160112310.1002/admi.201601123 ↗
4. 10.1002/adfm.20170728410.1002/adfm.201707284 ↗
5. 10.1126/sciadv.aat078810.1126/sciadv.aat0788 ↗
6. 10.1039/C8EE02779J10.1039/C8EE02779J ↗
7. 10.1021/acsami.8b0966110.1021/acsami.8b09661 ↗
8. 10.1039/C8EE03276A10.1039/C8EE03276A ↗
9. 10.1002/adma.20180356910.1002/adma.201803569 ↗
10. 10.1021/acsami.7b1693610.1021/acsami.7b16936 ↗
11. 10.1002/admi.20180001810.1002/admi.201800018 ↗
12. 10.1002/admi.20170021910.1002/admi.201700219 ↗
13. 10.1002/admi.20160035510.1002/admi.201600355 ↗
14. 10.1002/admi.20150021110.1002/admi.201500211 ↗
15. 10.1002/admi.20170086010.1002/admi.201700860 ↗
16. 10.1039/C5EE03109E10.1039/C5EE03109E ↗
17. 10.1016/j.cej.2019.03.00310.1016/j.cej.2019.03.003 ↗
18. 10.1039/C8NR10348H10.1039/C8NR10348H ↗
19. 10.1002/aenm.20180361210.1002/aenm.201803612 ↗
20. 10.1002/adma.20180065810.1002/adma.201800658 ↗
21. 10.1016/j.materresbull.2011.02.02810.1016/j.materresbull.2011.02.028 ↗
22. 10.1002/adma.20170289110.1002/adma.201702891 ↗
23. 10.1002/aenm.20180376810.1002/aenm.201803768 ↗
24. 10.1039/C7TC05564A10.1039/C7TC05564A ↗
25. 10.1039/c2ta01035f10.1039/c2ta01035f ↗
26. 10.1021/cm101532x10.1021/cm101532x ↗
27. 10.1039/C8NR04292F10.1039/C8NR04292F ↗
28. 10.1021/ja303056510.1021/ja3030565 ↗
29. 10.1039/C5TA03688G10.1039/C5TA03688G ↗
30. 10.1016/j.mseb.2013.03.01010.1016/j.mseb.2013.03.010 ↗
31. 10.1021/jp808826910.1021/jp8088269 ↗
32. 10.1039/c3nr00674c10.1039/c3nr00674c ↗
33. 10.1002/adfm.20150226510.1002/adfm.201502265 ↗
34. 10.1002/smll.20170275510.1002/smll.201702755 ↗
35. 10.1002/adfm.20180369510.1002/adfm.201803695 ↗
36. 10.1021/ja408421n10.1021/ja408421n ↗
37. 10.1016/j.jpowsour.2013.09.13010.1016/j.jpowsour.2013.09.130 ↗
38. 10.1016/j.nantod.2018.12.00410.1016/j.nantod.2018.12.004 ↗
39. 10.1002/aenm.20170325910.1002/aenm.201703259 ↗
40. 10.1002/aenm.20170217910.1002/aenm.201702179 ↗
41. 10.1021/acsnano.7b0752810.1021/acsnano.7b07528 ↗
42. 10.1002/adma.20150613310.1002/adma.201506133 ↗
43. 10.1002/aenm.20180398710.1002/aenm.201803987 ↗
44. 10.1002/anie.20190368410.1002/anie.201903684 ↗
45. 10.1039/C4GC02185A10.1039/C4GC02185A ↗
46. 10.1016/j.cej.2017.08.07010.1016/j.cej.2017.08.070 ↗
47. 10.1002/adma.20170571310.1002/adma.201705713 ↗
48. 10.1039/C5TA02210J10.1039/C5TA02210J ↗
49. 10.1039/c3nr00256j10.1039/c3nr00256j ↗
50. Wang Y. · Chem. Soc. Rev. · 2016 · 45
51. 10.1021/acsami.6b0541510.1021/acsami.6b05415 ↗
52. 10.1016/j.electacta.2017.12.03810.1016/j.electacta.2017.12.038 ↗
53. 10.1016/j.carbon.2014.12.00710.1016/j.carbon.2014.12.007 ↗
54. 10.1016/j.cej.2017.07.06310.1016/j.cej.2017.07.063 ↗
55. 10.1016/j.jcis.2015.12.02410.1016/j.jcis.2015.12.024 ↗
56. 10.1016/j.jallcom.2016.03.18510.1016/j.jallcom.2016.03.185 ↗
57. 10.1039/C6NR00468G10.1039/C6NR00468G ↗
58. 10.1016/j.nanoen.2018.08.05610.1016/j.nanoen.2018.08.056 ↗
59. 10.1038/nmat261210.1038/nmat2612 ↗
60. 10.1021/acsami.5b1064910.1021/acsami.5b10649 ↗
61. 10.1016/j.carbon.2016.11.05110.1016/j.carbon.2016.11.051 ↗
62. 10.1002/adfm.20170112210.1002/adfm.201701122 ↗
63. 10.1002/adma.20140204110.1002/adma.201402041 ↗
64. 10.1002/aenm.20140217610.1002/aenm.201402176 ↗
65. 10.1021/acsnano.5b0664810.1021/acsnano.5b06648 ↗
66. 10.1016/j.nanoen.2018.04.03210.1016/j.nanoen.2018.04.032 ↗
67. 10.1021/acsami.5b0314810.1021/acsami.5b03148 ↗
68. 10.1016/j.nanoen.2014.08.00110.1016/j.nanoen.2014.08.001 ↗
69. 10.1002/adma.20150564410.1002/adma.201505644 ↗
70. 10.1002/smll.20180523510.1002/smll.201805235 ↗
71. 10.1021/nl404008e10.1021/nl404008e ↗