42
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Engineered doping of organic semiconductors for enhanced thermoelectric efficiency.

      1 , , ,
      Nature materials

      Read this article at

      ScienceOpenPublisherPubMed
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Significant improvements to the thermoelectric figure of merit ZT have emerged in recent years, primarily due to the engineering of material composition and nanostructure in inorganic semiconductors (ISCs). However, many present high-ZT materials are based on low-abundance elements that pose challenges for scale-up, as they entail high material costs in addition to brittleness and difficulty in large-area deposition. Here we demonstrate a strategy to improve ZT in conductive polymers and other organic semiconductors (OSCs) for which the base elements are earth-abundant. By minimizing total dopant volume, we show that all three parameters constituting ZT vary in a manner so that ZT increases; this stands in sharp contrast to ISCs, for which these parameters have trade-offs. Reducing dopant volume is found to be as important as optimizing carrier concentration when maximizing ZT in OSCs. Implementing this strategy with the dopant poly(styrenesulphonate) in poly(3,4-ethylenedioxythiophene), we achieve ZT  =  0.42 at room temperature.

          Related collections

          Author and article information

          Journal
          Nat Mater
          Nature materials
          1476-1122
          1476-1122
          Aug 2013
          : 12
          : 8
          Affiliations
          [1 ] Department of Mechanical Engineering, University of Michigan, Ann Arbor, Michigan 48109-2125, USA.
          Article
          nmat3635
          10.1038/nmat3635
          23644522
          d3d593e2-ff8c-4cf2-aa3e-ff1d5ce974fc
          History

          Comments

          Comment on this article

          Related Documents Log