PEDOT:PSS Films With Very High Thermoelectric Properties Through Water‐Swollen Assisted Reduction With a Tetrakis(dimethylamino)ethylene Solution
Abstract Thermoelectric (TE) materials have attracted significant attention because they can be used to directly harvest waste heat into electricity. Organic TE materials like poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) have advantages including high mechanical flexibility, low cost, and low intrinsic thermal conductivity. However, their TE properties are notably inferior to their inorganic counterparts. Here, PEDOT:PSS films with very high thermoelectric properties through the sequential treatments with H 2 SO 4 , water, and ethanol solution of tetrakis(dimethylamino)ethylene (TDAE) are reported for the first time. The PEDOT:PSS films can exhibit a Seebeck coefficient of 58.2 µV K −1 and electrical conductivity of 1552 S cm −1 , and the corresponding power factor is 526 µW m −1 K −2 . The water treatment prior to the TDAE solution treatment is crucial for the high TE properties of PEDOT:PSS films. Without the water treatment, the control PEDOT:PSS films exhibit a Seebeck coefficient of only 32.4 µV K −1 and electrical conductivity of 1124 S cm −1 , and the corresponding power factor is only 118 µW m −1 K −2 . The effect of the water treatment on the Seebeck coefficient is attributed to the swelling of PEDOT:PSS films, which facilitates the penetration of TDAE from solution into the polymer films and thus the reduction of PEDOT:PSS.
Authors
- Yichen Xu (ORCID: https://orcid.org/0000-0002-1259-6185)
- Jianyong Ouyang (ORCID: https://orcid.org/0000-0001-9901-0177)
- Zhijun Chen (ORCID: https://orcid.org/0000-0001-7023-6519)
- Wen Sun
Institutions
- National University of Singapore (SG)
- Suzhou Research Institute (CN)
Publication Details
- Journal
- Advanced Functional Materials
- Published
- 2024-10-06
- DOI
- https://doi.org/10.1002/adfm.202410929
- Citations
- 22
- Primary Topic
- Advanced Thermoelectric Materials and Devices
- Type
- article
- Field-Weighted Citation Impact
- 2.58