journal article·2016-09-09

Statically Charged Electret Polymers as Solid, Nonvolatile Gates Encapsulating and Tuning Polymer Thermoelectric Parameters

R. M. Ireland, T. Jones, H. Li, H. Jang, J. E. West, H. E. Katz

ACS Energy Letters· Volume 1· Issue 3
Publisher page

Abstract

We report the first example of a free-standing charged electret gate associated with a thermoelectric material. Hydrophilic polymers, the commercially available fluorocarbon polymer Novec and a cross-linked polystyrene, were charged before and after deposition of the prototypical thiophene semiconducting polymer poly(bisdodecylquaterthiophene) (PQT12), respectively. Conductivity and Seebeck coefficient were measured. The charging modulated both parameters with the expected inverse dependences on charging-induced static voltage. A tetrafluorotetracyanoquinodimethane (F4TCNQ)-doped sample and the polystyrene sample displayed Seebeck coefficients close to predictions of a general model recently proposed for polymer thermoelectrics. The freestanding gate is a possible approach to modulating polymer thermoelectrics without disrupting intermolecular packing or applying gate voltages during operation.
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Research context

OpenAlex topics: Advanced Thermoelectric Materials and Devices · Transition Metal Oxide Nanomaterials · Thermal Radiation and Cooling Technologies

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

Affiliations

Department of Materials Science and Engineering and Department of Chemistry, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218, United States

Department of Electrical and Computer Engineering, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218, United States

Funding

Basic Energy Sciences

References (32)

Show source-provided references
1. 10.1002/aenm.20140107210.1002/aenm.201401072 ↗
2. 10.1021/ma402040610.1021/ma4020406 ↗
3. 10.1038/nmat363510.1038/nmat3635 ↗
4. 10.1038/nmat212010.1038/nmat2120 ↗
5. 10.1063/1.486722410.1063/1.4867224 ↗
6. 10.1021/ja305188r10.1021/ja305188r ↗
7. 10.1103/PhysRevLett.109.01660110.1103/PhysRevLett.109.016601 ↗
8. 10.1021/acsnano.5b0058910.1021/acsnano.5b00589 ↗
9. Huang C. · 2006 · 889 · 241
10. 10.1103/PhysRevLett.91.25680110.1103/PhysRevLett.91.256801 ↗
11. 10.1103/PhysRevLett.107.18660210.1103/PhysRevLett.107.186602 ↗
12. 10.1002/adfm.20140439710.1002/adfm.201404397 ↗
13. 10.1016/j.orgel.2015.11.02810.1016/j.orgel.2015.11.028 ↗
14. 10.1103/PhysRevB.81.07531610.1103/PhysRevB.81.075316 ↗
15. 10.1021/nl403079a10.1021/nl403079a ↗
16. 10.1063/1.489504610.1063/1.4895046 ↗
17. 10.1063/1.489397710.1063/1.4893977 ↗
18. 10.1007/s11664-014-3488-410.1007/s11664-014-3488-4 ↗
19. 10.1007/s10853-012-6856-610.1007/s10853-012-6856-6 ↗
20. 10.1063/1.323187310.1063/1.3231873 ↗
21. 10.1021/nl401482p10.1021/nl401482p ↗
22. 10.1143/APEX.2.12110310.1143/APEX.2.121103 ↗
23. 10.7567/APEX.8.05110110.7567/APEX.8.051101 ↗
24. 10.1021/nl502982f10.1021/nl502982f ↗
25. 10.1016/j.orgel.2009.10.00410.1016/j.orgel.2009.10.004 ↗
26. 10.1063/1.322285410.1063/1.3222854 ↗
27. 10.1063/1.238873010.1063/1.2388730 ↗
28. 10.1002/adfm.20060069010.1002/adfm.200600690 ↗
29. 10.1063/1.242692610.1063/1.2426926 ↗
30. 10.1021/am302221h10.1021/am302221h ↗
31. 10.1021/nn406406710.1021/nn4064067 ↗
32. 10.1016/j.orgel.2014.08.02310.1016/j.orgel.2014.08.023 ↗