Constructing a Hierarchical Ternary Hybrid of PEDOT:PSS/rGO/MoS2 as an Efficient Electrode for a Flexible Fiber-Shaped Supercapacitor
Source abstract
Abstract
Improving the specific capacitance and energy density of a fiber-shaped supercapacitor (FSSC) is critical to its applications as an energy storage device for advanced smart wearable electronics. In this paper, a heterogeneous poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)/reduced graphene oxide/molybdenum disulfide (PEDOT:PSS/rGO/MoS 2 ) fiber was prepared to achieve a high-performance and durable electrode for the FSSC. As indicated, pseudocapacitive MoS 2 was in situ grown on a highly conductive acid-treated PEDOT:PSS/rGO assembly with a hierarchical structure. This structural design emphasizes the wrinkled morphology and high conductivity of the PEDOT:PSS/rGO backbone to maximize the MoS 2 deposition and accelerate its electron transfer, which fully utilizes the pseudocapacitance of MoS 2 and provides additional capacitance contribution to the obtained device. Attributed to the synergy, the prepared fiber electrode in the FSSC exhibits high volumetric/areal specific capacitance (325.8 F cm –3 /405.3 mF cm –2 at 1 A cm –3 or 1.2 mA cm –2 ) and excellent rate performance (82%, 1–10 A cm –3 ). The corresponding device shows an ultrahigh volumetric energy density of 6.9 mW h cm –3 at a high power density of 173.6 mW cm –3 and an areal energy density of 8.5 μW h cm –2 at 215.9 μW cm –2, together with excellent cycle stability and mechanical flexibility, outperforming most of the previously reported FSSCs. Accordingly, the proposed strategy provides a great opportunity to develop a high-performance FSSC for further wearable electronics.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Advanced Sensor and Energy Harvesting Materials · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing International Science and Technology Cooperation Base of Carbon-Based Nanomaterials, Key Lab of Advanced Functional Materials, Ministry of Education, Faculty of Materials and Manufacturing, Beijing University of Technology, Beijing 100124, China
Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing 100190, China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Shandong Province · Beijing University of Technology
References (47)
Show source-provided references
1. 10.1039/d0cs01603a10.1039/d0cs01603a ↗
2. 10.1021/acs.chemrev.9b0046610.1021/acs.chemrev.9b00466 ↗
3. 10.1021/acs.chemrev.2c0019210.1021/acs.chemrev.2c00192 ↗
4. 10.1002/adma.20210432710.1002/adma.202104327 ↗
5. 10.1021/acsenergylett.8b0167510.1021/acsenergylett.8b01675 ↗
6. 10.1021/acs.nanolett.9b0140310.1021/acs.nanolett.9b01403 ↗
7. 10.1002/advs.20220385610.1002/advs.202203856 ↗
8. 10.1002/adma.20190180610.1002/adma.201901806 ↗
9. 10.1002/smtd.20210050210.1002/smtd.202100502 ↗
10. 10.1016/j.electacta.2020.13736310.1016/j.electacta.2020.137363 ↗
11. 10.1021/acsnano.8b0433610.1021/acsnano.8b04336 ↗
12. 10.1016/j.est.2022.10603210.1016/j.est.2022.106032 ↗
13. 10.1016/j.cej.2018.04.20710.1016/j.cej.2018.04.207 ↗
14. 10.1002/aenm.20160120810.1002/aenm.201601208 ↗
15. 10.1016/j.carbon.2020.09.09510.1016/j.carbon.2020.09.095 ↗
16. 10.1039/c8ta09328h10.1039/c8ta09328h ↗
17. 10.1021/acsaem.2c0104010.1021/acsaem.2c01040 ↗
18. 10.1002/aenm.20210339410.1002/aenm.202103394 ↗
19. 10.1021/acsami.6b0080810.1021/acsami.6b00808 ↗
20. 10.1016/j.carbon.2017.11.05210.1016/j.carbon.2017.11.052 ↗
21. 10.1021/acsaem.8b0090410.1021/acsaem.8b00904 ↗
22. 10.1002/anie.20141153310.1002/anie.201411533 ↗
23. 10.1016/j.carbon.2020.08.01710.1016/j.carbon.2020.08.017 ↗
24. 10.1016/j.jallcom.2019.15362210.1016/j.jallcom.2019.153622 ↗
25. 10.1016/j.ensm.2020.06.02010.1016/j.ensm.2020.06.020 ↗
26. 10.1016/j.carbon.2021.12.08810.1016/j.carbon.2021.12.088 ↗
27. 10.1016/j.electacta.2019.03.08410.1016/j.electacta.2019.03.084 ↗
28. 10.1039/c6ta09360d10.1039/c6ta09360d ↗
29. 10.1021/acsaem.2c0152410.1021/acsaem.2c01524 ↗
30. 10.1016/j.cej.2020.12456910.1016/j.cej.2020.124569 ↗
31. 10.1002/adma.20170097410.1002/adma.201700974 ↗
32. 10.1016/j.electacta.2019.13553010.1016/j.electacta.2019.135530 ↗
33. 10.1016/j.jpowsour.2019.22704410.1016/j.jpowsour.2019.227044 ↗
34. 10.1016/j.cej.2020.12567210.1016/j.cej.2020.125672 ↗
35. 10.1016/j.mtener.2017.09.01510.1016/j.mtener.2017.09.015 ↗
36. 10.1021/acsnano.9b0724410.1021/acsnano.9b07244 ↗
37. 10.1016/j.electacta.2017.05.01310.1016/j.electacta.2017.05.013 ↗
38. 10.1016/j.ensm.2017.01.00410.1016/j.ensm.2017.01.004 ↗
39. 10.1021/acsnano.6b0826210.1021/acsnano.6b08262 ↗
40. 10.1002/adma.20160068910.1002/adma.201600689 ↗
41. 10.1039/c6ta04081k10.1039/c6ta04081k ↗
42. 10.1038/srep0938710.1038/srep09387 ↗
43. 10.1039/c5cc10113a10.1039/c5cc10113a ↗
44. 10.1038/ncomms475410.1038/ncomms4754 ↗
45. 10.1039/c9ta01993f10.1039/c9ta01993f ↗
46. 10.1039/c5ta01990g10.1039/c5ta01990g ↗
47. 10.1016/j.jpcs.2019.01.00710.1016/j.jpcs.2019.01.007 ↗