Doping Engineering Enables Highly Conductive and Thermally Stable n-Type Organic Thermoelectrics with High Power Factor
Source abstract
Abstract
This work exploits the scope of doping engineering as an enabler for better-performing and thermally stable n-type organic thermoelectrics. A fullerene derivative with polar triethylene glycol type side chain (PTEG-1) is doped either by “coprocessing doping” with n-type dopants such as n-DMBI and TBAF or by “sequential doping” through thermal deposition of Cs2CO3. Solid-state diffusion of Cs2CO3 appears to dope PTEG-1 in the strongest manner, leading to the highest electrical conductivity of ∼7.5 S/cm and power factor of 32 μW/(m K2). Moreover, the behavior of differently doped PTEG-1 films under thermal stress is examined by electric and spectroscopic means. Cs2CO3-doped films are most stable, likely due to a coordinating interaction between the polar side chain and Cs+-based species, which immobilizes the dopant. The high power factor and good thermal stability of Cs2CO3-doped PTEG-1 make it very promising for tangible thermoelectric applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Thermoelectric Materials and Devices · Perovskite Materials and Applications · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Zernike Institute for Advanced Materials, Nijenborgh 4, NL-9747 AG Groningen, The Netherlands
Stratingh Institute for Chemistry, Nijenborgh 4, NL-9747 AG Groningen, The Netherlands
Funding
Stichting voor de Technische Wetenschappen · China Scholarship Council
References (46)
Show source-provided references
1. 10.3390/ma709670110.3390/ma7096701 ↗
2. 10.1039/C1EE02497C10.1039/C1EE02497C ↗
3. 10.1039/C6CP02830F10.1039/C6CP02830F ↗
4. 10.1002/adma.20130537110.1002/adma.201305371 ↗
5. 10.1126/science.115889910.1126/science.1158899 ↗
6. 10.1039/C6CS00149A10.1039/C6CS00149A ↗
7. 10.1038/natrevmats.2016.5010.1038/natrevmats.2016.50 ↗
8. 10.1021/jacs.7b0534410.1021/jacs.7b05344 ↗
9. 10.1038/nmat301210.1038/nmat3012 ↗
10. 10.1038/nmat363510.1038/nmat3635 ↗
11. 10.1002/adma.20130486610.1002/adma.201304866 ↗
12. 10.1016/j.nanoen.2018.07.00210.1016/j.nanoen.2018.07.002 ↗
13. 10.1002/aenm.20160211610.1002/aenm.201602116 ↗
14. 10.1126/sciadv.170043410.1126/sciadv.1700434 ↗
15. 10.1021/acsami.6b0563810.1021/acsami.6b05638 ↗
16. 10.1063/1.363163310.1063/1.3631633 ↗
17. 10.1021/acs.macromol.6b0231310.1021/acs.macromol.6b02313 ↗
18. 10.1016/j.nanoen.2018.07.05610.1016/j.nanoen.2018.07.056 ↗
19. 10.1002/adma.20180285010.1002/adma.201802850 ↗
20. 10.1002/adma.20170164110.1002/adma.201701641 ↗
21. 10.1021/jacs.5b0094510.1021/jacs.5b00945 ↗
22. 10.1002/adma.20160692810.1002/adma.201606928 ↗
23. 10.1002/adma.20180189810.1002/adma.201801898 ↗
24. 10.1002/adma.20180429010.1002/adma.201804290 ↗
25. 10.1002/aelm.20170058110.1002/aelm.201700581 ↗
26. 10.1021/acs.chemmater.7b0351610.1021/acs.chemmater.7b03516 ↗
27. 10.1002/adma.20170463010.1002/adma.201704630 ↗
28. 10.1021/acsenergylett.7b0114610.1021/acsenergylett.7b01146 ↗
29. 10.1021/acsenergylett.9b0097710.1021/acsenergylett.9b00977 ↗
30. 10.1002/ange.20160142010.1002/ange.201601420 ↗
31. 10.1002/adma.20170093010.1002/adma.201700930 ↗
32. 10.1002/aelm.20180095910.1002/aelm.201800959 ↗
33. 10.1002/admi.20150032410.1002/admi.201500324 ↗
34. 10.1002/adfm.20180327510.1002/adfm.201803275 ↗
35. 10.1002/aelm.20170050110.1002/aelm.201700501 ↗
36. 10.1039/C7TA06609K10.1039/C7TA06609K ↗
37. 10.1002/adma.20130058010.1002/adma.201300580 ↗
38. 10.1063/1.32415210.1063/1.324152 ↗
39. 10.1038/nmat463410.1038/nmat4634 ↗
40. 10.1002/adfm.20130306010.1002/adfm.201303060 ↗
41. 10.1039/c1jm11239b10.1039/c1jm11239b ↗
42. 10.1021/ja01506a04010.1021/ja01506a040 ↗
43. 10.1021/ar50122a00110.1021/ar50122a001 ↗
44. 10.1002/adma.20160373110.1002/adma.201603731 ↗
45. 10.1016/j.nanoen.2019.04.04010.1016/j.nanoen.2019.04.040 ↗
46. 10.1002/aenm.20170130510.1002/aenm.201701305 ↗