journal article·2015-10-14

All-Solid-State High-Energy Asymmetric Supercapacitors Enabled by Three-Dimensional Mixed-Valent MnOxNanospike and Graphene Electrodes

Jie Yang, Guizhu Li, Zhenghui Pan, Meinan Liu, Yuan Hou, Yijun Xu, Hong Deng, Leimei Sheng, Xinluo Zhao, Yongcai Qiu, Yuegang Zhang

Publisher page

Abstract

Three-dimensional (3D) nanostructures enable high-energy storage devices. Here we report a 3D manganese oxide nanospike (NSP) array electrode fabricated by anodization and subsequent electrodeposition. All-solid-state asymmetric supercapacitors were assembled with the 3D Al@Ni@MnOx NSP as the positive electrode, chemically converted graphene (CCG) as the negative electrode, and Na2SO4/poly(vinyl alcohol) (PVA) as the polymer gel electrolyte. Taking advantage of the different potential windows of Al@Ni@MnOx NSP and CCG electrodes, the asymmetric supercapacitor showed an ideal capacitive behavior with a cell voltage up to 1.8 V, capable of lighting up a red LED indicator (nominal voltage of 1.8 V). The device could deliver an energy density of 23.02 W h kg(-1) at a current density of 1 A g(-1). It could also preserve 96.3% of its initial capacitance at a current density of 2 A g(-1) after 10000 charging/discharging cycles. The remarkable performance is attributed to the unique 3D NSP array structure that could play an important role in increasing the effective electrode surface area, facilitating electrolyte permeation, and shortening the electron pathway in the active materials.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supercapacitor Materials and Fabrication · Advanced battery technologies research · Conducting polymers and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

i-Lab, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Science, Suzhou 215123, China

Department of Physics, Institute of Low-Dimensional Carbons and Device Physics, Shanghai University, Shanghai 200444, China,

School of Chemistry and Environment, South China Normal University, Guangzhou 510006, China

Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States

Department of Physics, Tsinghua University, Beijing 100084, China

Funding

National Natural Science Foundation of China · China Postdoctoral Science Foundation · Natural Science Foundation of Guangdong Province · Program for New Century Excellent Talents in University · Natural Science Foundation of Jiangsu Province

References (54)

Show source-provided references
1. 10.1021/am302280b10.1021/am302280b ↗
2. 10.1021/nl301804c10.1021/nl301804c ↗
3. 10.1039/c3nr06650a10.1039/c3nr06650a ↗
4. 10.1002/adma.20130475610.1002/adma.201304756 ↗
5. 10.1021/nn100856y10.1021/nn100856y ↗
6. 10.1039/c3nr06675d10.1039/c3nr06675d ↗
7. 10.1021/nn401450s10.1021/nn401450s ↗
8. 10.1016/j.nanoen.2014.08.00110.1016/j.nanoen.2014.08.001 ↗
9. 10.1002/aenm.20130099410.1002/aenm.201300994 ↗
10. 10.1039/C2NR33136E10.1039/C2NR33136E ↗
11. 10.1039/c3ee40509e10.1039/c3ee40509e ↗
12. 10.1039/c1ee01354h10.1039/c1ee01354h ↗
13. 10.1039/C2NR32040A10.1039/C2NR32040A ↗
14. 10.1016/j.nanoen.2014.09.01010.1016/j.nanoen.2014.09.010 ↗
15. 10.1016/j.nanoen.2014.09.03310.1016/j.nanoen.2014.09.033 ↗
16. 10.1016/j.jpowsour.2013.03.08310.1016/j.jpowsour.2013.03.083 ↗
17. 10.1021/nn304833s10.1021/nn304833s ↗
18. 10.1021/nn101754k10.1021/nn101754k ↗
19. 10.1039/C5TC00157A10.1039/C5TC00157A ↗
20. 10.1016/j.nanoen.2014.11.06310.1016/j.nanoen.2014.11.063 ↗
21. 10.1039/c3nr06675d10.1039/c3nr06675d ↗
22. 10.1039/c3ta14387b10.1039/c3ta14387b ↗
23. 10.1002/adfm.20110005810.1002/adfm.201100058 ↗
24. 10.1016/j.jpowsour.2007.08.11510.1016/j.jpowsour.2007.08.115 ↗
25. 10.1016/j.nanoen.2014.08.01910.1016/j.nanoen.2014.08.019 ↗
26. 10.1002/aenm.20120038010.1002/aenm.201200380 ↗
27. 10.1016/j.ssi.2013.03.01410.1016/j.ssi.2013.03.014 ↗
28. 10.1016/j.jpowsour.2011.06.03210.1016/j.jpowsour.2011.06.032 ↗
29. 10.1016/j.elecom.2010.01.03210.1016/j.elecom.2010.01.032 ↗
30. 10.1126/science.123908910.1126/science.1239089 ↗
31. 10.1007/s00339-005-3397-810.1007/s00339-005-3397-8 ↗
32. 10.1016/j.jpowsour.2009.06.06810.1016/j.jpowsour.2009.06.068 ↗
33. 10.1021/nn203085j10.1021/nn203085j ↗
34. 10.1007/s00339-005-3401-310.1007/s00339-005-3401-3 ↗
35. 10.1063/1.12100410.1063/1.121004 ↗
36. 10.1039/C3TC31476F10.1039/C3TC31476F ↗
37. 10.1002/adma.20120506410.1002/adma.201205064 ↗
38. 10.1149/1.213182110.1149/1.2131821 ↗
39. 10.1039/a807821a10.1039/a807821a ↗
40. Xiao F. · Int. J. Electrochem. Sci. · 2012 · 7 · 744010.1016/S1452-3981(23)15795-6 ↗
41. 10.1021/nl300984y10.1021/nl300984y ↗
42. Conway B. E. · 199910.1007/978-1-4757-3058-6 ↗
43. 10.1021/am300455d10.1021/am300455d ↗
44. 10.1039/C2TC00235C10.1039/C2TC00235C ↗
45. 10.1039/C1JM13872C10.1039/C1JM13872C ↗
46. 10.1016/j.electacta.2015.01.22310.1016/j.electacta.2015.01.223 ↗
47. 10.1039/C4TA03096F10.1039/C4TA03096F ↗
48. 10.1016/j.jpowsour.2011.09.00510.1016/j.jpowsour.2011.09.005 ↗
49. 10.1016/j.jpowsour.2005.03.21010.1016/j.jpowsour.2005.03.210 ↗
50. 10.1039/C5TA01990G10.1039/C5TA01990G ↗
51. 10.1021/acsami.5b0215710.1021/acsami.5b02157 ↗
52. 10.1016/j.nanoen.2014.06.01310.1016/j.nanoen.2014.06.013 ↗
53. 10.1002/adma.20120341010.1002/adma.201203410 ↗
54. 10.1039/C5TA02685G10.1039/C5TA02685G ↗