Capacitance-Enhanced Microsupercapacitors with a Redox Electrolyte Additive for an All-MXene-Based Flexible Self-Powered Integrated Photodetecting System
Source abstract
Abstract
Although much effort has been devoted to improving the electrochemical performances of MXene-based metal-ion hybrid microsupercapacitors (MSCs), few works focus on the electrolyte. Therefore, we proposed K 4 Fe(CN) 6 as the redox additive to alter the properties of the Zn(CF 3 SO 3 ) 2 gel electrolyte used in Ti 3 C 2 T x -DMAC MXene-based interdigital Zn-ion hybrid MSCs. The electron transfers between Fe 2+ and Fe 3+ in K 4 Fe(CN) 6 can provide an additional Faraday pseudocapacitance, resulting in the high volumetric capacitance (2107.4 F cm –3 at a scan rate of 5 mV s –1 ) of the MSCs and excellent cycling stability with 88.64% of the original capacity retention after 5000 cycles of charge and discharge. Such a superior performance of MSCs can provide a potential of 0.9 V for the integrated Ti 3 C 2 T x -DCTES MXene-based photodetector, which endows the detector with a stable response to 808 nm wavelength laser, providing a strong support for flexible self-powered integrated sensing systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: MXene and MAX Phase Materials · Supercapacitor Materials and Fabrication · Advanced Sensor and Energy Harvesting Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Integrated Circuits and Electronics, Beijing Institute of Technology, Beijing 100081, China
Funding
National Natural Science Foundation of China · Beijing Institute of Technology Research Fund Program for Young Scholars · Beijing Science and Technology Planning Project
References (36)
Show source-provided references
1. 10.1016/j.nanoen.2022.10773910.1016/j.nanoen.2022.107739 ↗
2. 10.1002/smll.20220436510.1002/smll.202204365 ↗
3. 10.1038/s41467-021-23744-210.1038/s41467-021-23744-2 ↗
4. 10.1007/s40820-021-00757-610.1007/s40820-021-00757-6 ↗
5. 10.1007/s40820-020-00546-710.1007/s40820-020-00546-7 ↗
6. 10.1002/advs.20210077510.1002/advs.202100775 ↗
7. 10.1002/admi.20220116510.1002/admi.202201165 ↗
8. 10.1002/anie.20211064010.1002/anie.202110640 ↗
9. 10.1002/adfm.20210400710.1002/adfm.202104007 ↗
10. 10.1016/j.apsusc.2019.14425010.1016/j.apsusc.2019.144250 ↗
11. 10.1039/C6RA06797B10.1039/C6RA06797B ↗
12. 10.1002/adfm.20160574510.1002/adfm.201605745 ↗
13. 10.1016/j.jpowsour.2014.01.06210.1016/j.jpowsour.2014.01.062 ↗
14. 10.1016/j.jscs.2018.02.00110.1016/j.jscs.2018.02.001 ↗
15. 10.1002/admt.20220015810.1002/admt.202200158 ↗
16. 10.1016/j.jpowsour.2015.12.03410.1016/j.jpowsour.2015.12.034 ↗
17. 10.1016/j.ijhydene.2016.02.05210.1016/j.ijhydene.2016.02.052 ↗
18. 10.1038/nature1397010.1038/nature13970 ↗
19. 10.1016/j.electacta.2011.06.03910.1016/j.electacta.2011.06.039 ↗
20. 10.1007/s11581-015-1546-410.1007/s11581-015-1546-4 ↗
21. 10.1617/s11527-015-0583-910.1617/s11527-015-0583-9 ↗
22. 10.1016/j.molstruc.2017.03.03610.1016/j.molstruc.2017.03.036 ↗
23. 10.1007/s10965-016-1043-010.1007/s10965-016-1043-0 ↗
24. 10.1016/j.electacta.2020.13693710.1016/j.electacta.2020.136937 ↗
25. 10.1002/adfm.20190413610.1002/adfm.201904136 ↗
26. 10.1007/s40820-021-00634-210.1007/s40820-021-00634-2 ↗
27. 10.1021/acsnano.7b0139010.1021/acsnano.7b01390 ↗
28. 10.1039/C7TA02936E10.1039/C7TA02936E ↗
29. 10.1002/ange.20190368410.1002/ange.201903684 ↗
30. 10.1002/admt.20160028210.1002/admt.201600282 ↗
31. 10.1021/acsaem.0c0030910.1021/acsaem.0c00309 ↗
32. 10.1016/0022-4596(82)90225-010.1016/0022-4596(82)90225-0 ↗
33. 10.1002/aenm.20120026710.1002/aenm.201200267 ↗
34. 10.1142/S179360472141005810.1142/S1793604721410058 ↗
35. 10.1007/s40820-022-00924-310.1007/s40820-022-00924-3 ↗
36. 10.1016/j.cej.2021.12948910.1016/j.cej.2021.129489 ↗