journal article·2020-12-01Open access

MXene improves the stability and electrochemical performance of electropolymerized PEDOT films

Shofarul Wustoni, Abdulelah Saleh, Jehad K. El-Demellawi, Anil Koklu, Adel Hama, Victor Druet, Nimer Wehbe, Yizhou Zhang, Sahika Inal

APL Materials· Volume 8· Issue 12

Abstract

Poly(3,4-ethylenedioxythiophene) (PEDOT) doped with poly(styrene sulfonate) (PSS) is the most commonly used conducting polymer in organic bioelectronics. However, electrochemical capacitances exceeding the current state-of-the-art are required for enhanced transduction and stimulation of biological signals. The long-term stability of conducting polymer films during device operation and storage in aqueous environments remains a challenge for routine applications. In this work, we electrochemically synthesize a PEDOT composite comprising the water dispersible two-dimensional conducting material Ti3C2 MXene. We find that incorporating MXene as a co-dopant along with PSS leads to PEDOT:PSS:MXene films with remarkably high volumetric capacitance (607.0 ± 85.3 F cm−3) and stability (capacity retention = 78.44% ± 1.75% over 500 cycles), outperforming single dopant-comprising PEDOT films, i.e., PEDOT:PSS and PEDOT:MXene electropolymerized under the same conditions on identical surfaces. The stability of microfabricated PEDOT:PSS:MXene electrodes is evaluated under different conditions, i.e., when the films are exposed to sonication (∼100% retention over 6 min), upon immersion in cell culture media for 14 days (∆|Z| = 2.13%), as well as after continuous electrical stimulation. Furthermore, we demonstrate the use of a PEDOT:PSS:MXene electrode as an electrochemical sensor for sensitive detection of dopamine (DA). The sensor exhibited an enhanced electrocatalytic activity toward DA in a linear range from 1 µM to 100 μM validated in mixtures containing common interferents such as ascorbic acid and uric acid. PEDOT:PSS:MXene composite is easily formed on conductive substrates with various geometries and can serve as a high performance conducting interface for chronic biochemical sensing or stimulation applications.
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Research context

OpenAlex topics: MXene and MAX Phase Materials · Advanced Sensor and Energy Harvesting Materials · Conducting polymers and applications

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

Affiliations

Organic Bioelectronics Laboratory, Biological and Environmental Science and Engineering (BESE), King Abdullah University of Science and Technology (KAUST) 1 , Thuwal 23955-6900, Saudi Arabia

Physical Science and Engineering (PSE), KAUST 2 , Thuwal 23955-6900, Saudi Arabia

Imaging and Characterizations Core Labs, KAUST 3 , Thuwal 23955-6900, Saudi Arabia

Funding

King Abdullah University of Science and Technology

References (69)

Show source-provided references
1. Acta Biomater. · 2014 · 10 · 234110.1016/j.actbio.2014.02.015 ↗
2. Adv. Electron. Mater. · 2015 · 1 · 150001710.1002/aelm.201500017 ↗
3. Nat. Commun. · 2016 · 7 · 1128710.1038/ncomms11287 ↗
4. Adv. Funct. Mater. · 2017 · 27 · 170032910.1002/adfm.201700329 ↗
5. J. Mater. Chem. A · 2014 · 2 · 1705810.1039/c4ta03603d ↗
6. Mater. Sci. Eng. R: Rep. · 2020 · 140 · 10054610.1016/j.mser.2020.100546 ↗
7. Nat. Commun. · 2019 · 10 · 104310.1038/s41467-019-09003-5 ↗
8. Synth. Met. · 2016 · 220 · 39410.1016/j.synthmet.2016.07.010 ↗
9. NPG Asia Mater. · 2018 · 10 · 25510.1038/s41427-018-0014-9 ↗
10. Sci. Adv. · 2020 · 6 · eaay539410.1126/sciadv.aay5394 ↗
11. Sci. Adv. · 2017 · 3 · e160044810.1126/sciadv.1600448 ↗
12. Aguilar · 2019 · 191
13. Sens. Actuators, B · 2003 · 89 · 9210.1016/s0925-4005(02)00448-3 ↗
14. Polym. J. · 2019 · 51 · 102910.1038/s41428-019-0213-4 ↗
15. ACS Mater. Lett. · 2019 · 1 · 59910.1021/acsmaterialslett.9b00373 ↗
16. Adv. Funct. Mater. · 2019 · 29 · 190440310.1002/adfm.201904403 ↗
17. ACS Omega · 2018 · 3 · 742410.1021/acsomega.8b00458 ↗
18. Jpn. J. Appl. Phys. · 2016 · 55 · 06GK0310.7567/jjap.55.06gk03 ↗
19. Macromol. Biosci. · 2016 · 16 · 122710.1002/mabi.201600059 ↗
20. Front. Neuroeng. · 2012 · 5 · 810.3389/fneng.2012.00008 ↗
21. J. Mater. Chem. B · 2014 · 2 · 520910.1039/c4tb00789a ↗
22. Macromol. Biosci. · 2012 · 12 · 49410.1002/mabi.201100490 ↗
23. Chem. Commun. · 2004 · 82010.1039/b316794a ↗
24. Chem. Commun. · 2002 · 68010.1039/b111728a ↗
25. Adv. Mater. Interfaces · 2019 · 6 · 180092810.1002/admi.201800928 ↗
26. Adv. Mater. Technol. · 2020 · 5 · 190094310.1002/admt.201900943 ↗
27. ACS Appl. Mater. Interfaces · 2015 · 7 · 1538810.1021/acsami.5b03350 ↗
28. Synth. Met. · 2019 · 248 · 4510.1016/j.synthmet.2018.12.010 ↗
29. Nat. Energy · 2017 · 2 · 1710510.1038/nenergy.2017.105 ↗
30. Adv. Mater. · 2017 · 29 · 170267810.1002/adma.201702678 ↗
31. Adv. Mater. · 2014 · 26 · 99210.1002/adma.201304138 ↗
32. Adv. Mater. · 2020 · 32 · 190848610.1002/adma.201908486 ↗
33. ACS Mater. Lett. · 2020 · 2 · 5510.1021/acsmaterialslett.9b00419 ↗
34. Nano Energy · 2019 · 60 · 73410.1016/j.nanoen.2019.04.002 ↗
35. Joule · 2019 · 3 · 16410.1016/j.joule.2018.10.017 ↗
36. Adv. Funct. Mater. · 2018 · 28 · 170380810.1002/adfm.201703808 ↗
37. Dalton Trans. · 2019 · 48 · 174710.1039/c8dt04374d ↗
38. Chin. Chem. Lett. · 2020 · 31 · 101810.1016/j.cclet.2019.11.031 ↗
39. Front. Mater. · 2019 · 6 · 31210.3389/fmats.2019.00312 ↗
40. J. Mater. Chem. A · 2014 · 2 · 1433410.1039/c4ta02638a ↗
41. Chem. Mater. · 2017 · 29 · 484810.1021/acs.chemmater.7b00745 ↗
42. npj 2D Mater. Appl. · 2019 · 3 · 810.1038/s41699-019-0089-3 ↗
43. Chem. Mater. · 2017 · 29 · 763310.1021/acs.chemmater.7b02847 ↗
44. ACS Nano · 2018 · 12 · 848510.1021/acsnano.8b04029 ↗
45. Energy Environ. Sci. · 2016 · 9 · 284710.1039/c6ee01717g ↗
46. RSC Adv. · 2015 · 5 · 7972910.1039/c5ra13976g ↗
47. Energy Environ. Sci. · 2013 · 6 · 195610.1039/c3ee41077c ↗
48. Sci. Rep. · 2016 · 6 · 1880510.1038/srep18805 ↗
49. Sci. Rep. · 2018 · 8 · 1529310.1038/s41598-018-33521-9 ↗
50. ACS Cent. Sci. · 2016 · 2 · 66710.1021/acscentsci.6b00220 ↗
51. RSC Adv. · 2019 · 9 · 4249810.1039/c9ra10250g ↗
52. J. Phys. Chem. C · 2018 · 122 · 19410.1021/acs.jpcc.7b10582 ↗
53. ACS Appl. Polym. Mater. · 2019 · 1 · 310310.1021/acsapm.9b00757 ↗
54. Macromolecules · 1999 · 32 · 680710.1021/ma9905674 ↗
55. Electrochim. Acta · 2017 · 235 · 34810.1016/j.electacta.2017.03.069 ↗
56. Chin. J. Polym. Sci. · 2015 · 33 · 101810.1007/s10118-015-1647-6 ↗
57. J. Mater. · 2020 · 6 · 13810.1016/j.jmat.2019.12.013 ↗
58. J. Phys. Chem. Lett. · 2018 · 9 · 122310.1021/acs.jpclett.8b00200 ↗
59. IEEE Trans. Biomed. Eng. · 2006 · 53 · 32010.1109/tbme.2005.862552 ↗
60. Biotechnol. J. · 2011 · 6 · 60010.1002/biot.201000355 ↗
61. Nat. Rev. Neurosci. · 2004 · 5 · 48310.1038/nrn1406 ↗
62. Nat. Rev. Neurosci. · 2002 · 3 · 93210.1038/nrn983 ↗
63. J. Electroanal. Chem. · 2008 · 614 · 11310.1016/j.jelechem.2007.11.007 ↗
64. ACS Appl. Mater. Interfaces · 2018 · 10 · 2583410.1021/acsami.7b07668 ↗
65. Electroanalysis · 2014 · 26 · 54810.1002/elan.201300547 ↗
66. Anal. Chem. · 2019 · 91 · 1291710.1021/acs.analchem.9b02904 ↗
67. Electrochim. Acta · 2015 · 154 · 19710.1016/j.electacta.2014.12.046 ↗
68. Sci. Rep. · 2016 · 6 · 3541910.1038/srep35419 ↗
69. Talanta · 2020 · 210 · 12062610.1016/j.talanta.2019.120626 ↗