Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 9, Issue 19, Pages 11787-11793Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta01645h
Keywords
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Funding
- A*STAR Computational Resource Centre
- A*STAR [1527200019, 1527200021, A19D9a0096]
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The study of n-doped conjugated polymers has accelerated the development of n-type polymer thermoelectrics, with outstanding thermoelectric performance achieved by doping an old ladder-type conjugated polymer with an old organic radical. This demonstrates the importance of electrochemically active counter cations for electron transport and higher conductivity in n-type organic semiconductors.
Over the past five years, the understanding of n-doped conjugated polymers has greatly accelerated the science of n-type polymer thermoelectrics. Part of this rapid progress is based on the emergence of new high-performance n-type conjugated polymers. n-Dopants, on the other hand, have not shown a significant breakthrough. Here we show that one of the oldest ladder-type conjugated polymers, poly(benzimidazobenzophenanthrolinedione) (BBL), can have outstanding n-type thermoelectric performance and superior thermal stability (100 degrees C over 4 days) when n-doped with one of the oldest organic radicals, the benzyl viologen radical cation (BV+). The BV+-doped BBL films achieved a maximum conductivity of 1.63 (1.60 +/- 0.05) S cm(-1) and a power factor of 5.37 (4.85 +/- 0.46) mu W m(-1) K-2 in large channel devices (channel length = 2.5 mm; channel width = 20 mm), which are among the highest reported in the literature for n-type polymers, making them the best BBL based n-type thermoelectrics. The enhanced thermoelectric properties of the BV+-doped BBL are a consequence of the electrochemically active BV+/2+ molecules facilitating electron transport between the BBL fibers. Our results suggest that an electrochemically active counter cation is necessary for better electron transport and thus higher conductivity in fiber-forming/(semi)crystalline n-type organic semiconductors. The same is also likely to be true when the counter anion is electrochemically active for fiber-forming/(semi)crystalline p-type organic semiconductors. These findings will have tremendous impact on the chemical design of p- and n-dopants for organic semiconductors in the future.
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