Gate Field Induced Extraordinary Energy Storage in MoS2-Graphene-Based Ultramicro-Electrochemical Capacitor
Source abstract
Abstract
On-chip microscopic energy systems have revolutionized device design for miniaturized energy storage systems. Many atomically thin materials have provided a unique opportunity to develop highly efficient small-scale devices. We report an ultramicro-electrochemical capacitor with two-dimensional (2D) molybdenum disulphide (MoS 2 ) and graphene-based electrodes. Due to the tunable density of states, 2D MoS 2 provides electric field-induced doping and, combined with a graphene interface, leads to a high carrier mobility. The fabricated solid-state energy storage device is obtained using a gel electrolyte that provides an electrochemical capacitance of 1.8 mF/cm 2 . An extraordinary enhancement of ∼3000% in electrochemical capacitance (55 mF/cm 2 from 1.8 mF/cm 2, measured from a cyclic voltammetry curve) is observed upon application of back-gate field of −25 V, which is more than the enhancement (18%) observed in a MoS 2 electrochemical capacitor (0.95 mF/cm 2 from 0.8 mF/cm 2 ) without graphene, whereas the galvanic charge–discharge measurements analysis shows ∼1677% enhancement under the application of −25 V back-gate voltage. Thus, the electric field-induced doping in 2D MoS 2, in addition to a high charge carrier mobility due to the graphene, plays a crucial role in an extraordinary large energy storage in the ultramicro-electrochemical capacitor. We also evaluated the capacitance response using an AC signal superimposed with the DC bias to investigate the influence of polarization potential on the electrolyte. The study provides a benchmark development of an ultramicro-electrochemical capacitor for ultrahigh charge storage capability.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · 2D Materials and Applications · MXene and MAX Phase Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Instrumentation and Applied Physics, Indian Institute of Science, Bangalore 560012, Karnataka, India
Funding
Indian Institute of Science
References (55)
Show source-provided references
1. 10.1039/D1TA09334G10.1039/D1TA09334G ↗
2. 10.1016/j.nanoen.2018.05.00210.1016/j.nanoen.2018.05.002 ↗
3. 10.1016/j.electacta.2018.05.19810.1016/j.electacta.2018.05.198 ↗
4. 10.1039/C7TA07960E10.1039/C7TA07960E ↗
5. 10.1002/smll.20160083510.1002/smll.201600835 ↗
6. 10.1038/nnano.2014.20710.1038/nnano.2014.207 ↗
7. 10.1038/nphoton.2017.7510.1038/nphoton.2017.75 ↗
8. 10.1039/C6RA22496B10.1039/C6RA22496B ↗
9. 10.1016/j.physe.2020.11424310.1016/j.physe.2020.114243 ↗
10. 10.1016/j.jpcs.2020.10933110.1016/j.jpcs.2020.109331 ↗
11. 10.1038/nnano.2013.10010.1038/nnano.2013.100 ↗
12. 10.1002/aelm.20200083810.1002/aelm.202000838 ↗
13. 10.1016/j.apmt.2018.09.00310.1016/j.apmt.2018.09.003 ↗
14. 10.1364/OE.42185710.1364/OE.421857 ↗
15. 10.1103/PhysRevApplied.14.05401410.1103/PhysRevApplied.14.054014 ↗
16. 10.1016/j.jallcom.2020.15455710.1016/j.jallcom.2020.154557 ↗
17. 10.1016/j.apsusc.2020.14764410.1016/j.apsusc.2020.147644 ↗
18. 10.1038/s41528-020-00093-610.1038/s41528-020-00093-6 ↗
19. 10.1039/C6EE01717G10.1039/C6EE01717G ↗
20. 10.1002/aenm.20130126910.1002/aenm.201301269 ↗
21. 10.1016/j.sse.2018.10.00110.1016/j.sse.2018.10.001 ↗
22. 10.1021/nl301335q10.1021/nl301335q ↗
23. 10.1016/j.ssc.2007.01.05010.1016/j.ssc.2007.01.050 ↗
24. 10.1038/srep1044010.1038/srep10440 ↗
25. 10.1038/s41467-020-17006-w10.1038/s41467-020-17006-w ↗
26. 10.1103/PhysRevApplied.14.05401410.1103/PhysRevApplied.14.054014 ↗
27. 10.1016/j.rser.2020.11002610.1016/j.rser.2020.110026 ↗
28. 10.1021/nn503570j10.1021/nn503570j ↗
29. 10.5796/electrochemistry.81.77710.5796/electrochemistry.81.777 ↗
30. 10.1021/nl200225j10.1021/nl200225j ↗
31. 10.1002/adma.20170267810.1002/adma.201702678 ↗
32. 10.1016/j.nanoen.2016.06.03010.1016/j.nanoen.2016.06.030 ↗
33. 10.1016/j.jpowsour.2016.10.09110.1016/j.jpowsour.2016.10.091 ↗
34. 10.1016/j.electacta.2019.13553610.1016/j.electacta.2019.135536 ↗
35. 10.1007/s12274-018-2096-710.1007/s12274-018-2096-7 ↗
36. 10.1016/j.ceramint.2021.11.31610.1016/j.ceramint.2021.11.316 ↗
37. 10.1002/smtd.20190008110.1002/smtd.201900081 ↗
38. 10.1021/acsami.7b0607110.1021/acsami.7b06071 ↗
39. 10.1021/acsnano.9b1018210.1021/acsnano.9b10182 ↗
40. 10.1021/acsnano.5b0008710.1021/acsnano.5b00087 ↗
41. 10.1007/s00289-022-04495-610.1007/s00289-022-04495-6 ↗
42. 10.1021/acs.chemmater.9b0065510.1021/acs.chemmater.9b00655 ↗
43. 10.1002/adfm.20191043910.1002/adfm.201910439 ↗
44. 10.1246/cl.1998.118910.1246/cl.1998.1189 ↗
45. 10.1039/C4RA05151C10.1039/C4RA05151C ↗
46. 10.3390/ma1416459010.3390/ma14164590 ↗
47. 10.1002/aenm.20170057110.1002/aenm.201700571 ↗
48. 10.1021/cr00090a00310.1021/cr00090a003 ↗
49. 10.1063/1.513184510.1063/1.5131845 ↗
50. 10.1002/smll.20170103910.1002/smll.201701039 ↗
51. 10.1021/acs.nanolett.2c0125010.1021/acs.nanolett.2c01250 ↗
52. 10.1021/acs.jpcc.8b0989810.1021/acs.jpcc.8b09898 ↗
53. 10.1039/C7TC00800G10.1039/C7TC00800G ↗
54. 10.1021/jz200879a10.1021/jz200879a ↗
55. 10.1002/adfm.20110005810.1002/adfm.201100058 ↗