Affiliation:
1. Center for Applied Energy Research University of Kentucky Lexington KY 40506 USA
2. Department of Chemical and Materials Engineering Center for Applied Energy Research University of Kentucky Lexington KY 40506 USA
3. Department of Chemistry Purdue University West Lafayette IN 47907 USA
4. Department of Chemistry University of Kentucky Lexington KY 40506 USA
Abstract
AbstractThe field of electronic textiles currently lacks n‐type polymer fibers that can complement the more established p‐type polymer fibers. Here, a highly conductive n‐type polymer fiber is obtained via wet‐spinning of n‐doped poly(3,7‐dihydrobenzo[1,2‐b:4,5‐b’]difuran‐2,6‐dione) (n‐PBDF). The electrical conductivity of the fibers increases from 1000 to 1600 S cm−1 with increased draw during processing and correlates well with Young's modulus. Wide‐angle X‐ray scattering reveals the existence of a bimodal orientation of the polymer chains, favoring parallel alignment to the fiber axis with increased draw. After 14 d in 80% humid air, fiber conductivity stabilizes maintaining 81% of the initial conductivity. Although the electrical conductivity drops slightly over time, the Seebeck coefficient increases, resulting in the highest thermoelectric power factor being measured at 91 µW m−1 K−2 for the most drawn fiber 14 d after its fabrication. A proof‐of‐concept two‐couple thermoelectric textile is crafted by embroidering bundles of n‐type PBDF fibers and p‐type PEDOT:PSS fibers. The device generates 2.40 nW at a 22 °C temperature gradient. This work represents the initial steps and a crucial advancement toward fabricating high‐performance n‐type polymer fibers that can complement their p‐type counterparts to close the existing performance gap.
Funder
Office of Naval Research
National Science Foundation
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
5 articles.
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