Polymer morphology and interfacial charge transfer dominate over energy-dependent scattering in organic-inorganic thermoelectrics

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Polymer morphology and interfacial charge transfer dominate over energy-dependent scattering in organic-inorganic thermoelectrics
Title:
Polymer morphology and interfacial charge transfer dominate over energy-dependent scattering in organic-inorganic thermoelectrics
Journal Title:
Nature Communications
Keywords:
Publication Date:
17 December 2018
Citation:
Kumar, P., Zaia, E.W., Yildirim, E. et al. Polymer morphology and interfacial charge transfer dominate over energy-dependent scattering in organic-inorganic thermoelectrics. Nat Commun 9, 5347 (2018). https://doi.org/10.1038/s41467-018-07435-z
Abstract:
Hybrid (organic-inorganic) materials have emerged as a promising class of thermoelectric materials, achieving power factors (S2σ) exceeding those of either constituent. The mechanism of this enhancement is still under debate, and pinpointing the underlying physics has proven difficult. In this work, we combine transport measurements with theoretical simulations and first principles calculations on a prototypical PEDOT:PSS-Te(Cux) nanowire hybrid material system to understand the effect of templating and charge redistribution on the thermoelectric performance. Further, we apply the recently developed Kang-Snyder charge transport model to show that scattering of holes in the hybrid system, defined by the energy-dependent scattering parameter, remains the same as in the host polymer matrix; performance is instead dictated by polymer morphology manifested in an energy-independent transport coefficient. We build upon this language to explain thermoelectric behavior in a variety of PEDOT and P3HT based hybrids acting as a guide for future work in multiphase materials.
License type:
http://creativecommons.org/licenses/by/4.0/
Funding Info:
This work was partially performed at the Molecular Foundry, Lawrence Berkeley National Laboratory, and was supported by the Department of Energy, Office of Science, Office of Basic Energy Sciences, Scientific User Facilities Division of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. This work was also partially performed at the Agency for Science, Technology, and Research, supported by the Science and Energy Research Council under the Pharos grants 1527200018 and 1527200024. EWZ gratefully acknowledges the National Science Foundation for fellowship support under the National Science Foundation Graduate Research Fellowship Program.
Description:
ISSN:
2041-1723
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