4.8 Article

Lactone Backbone Density in Rigid Electron-Deficient Semiconducting Polymers Enabling High n-type Organic Thermoelectric Performance

期刊

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202113078

关键词

chemical doping; metal-free polymerization; organic thermoelectrics; rigid semiconducting polymers; synthetic methods

资金

  1. KAUST
  2. Office of Sponsored Research (OSR) [OSR-2018-CRG/CCF-3079, OSR-2019-CRG8-4086, OSR-2018-CRG7-3749]
  3. ERC Synergy Grant SC2 [610115]
  4. European Union's Horizon 2020 research and innovation program [952911, 862474]
  5. EPSRC Project [EP/T026219/1B]
  6. National Science Foundation [NSF DMR-1751308]
  7. DOE Office of Science [DE-AC02-06CH11357]
  8. Knut and Alice Wallenberg foundation
  9. Swedish Research Council [2020-03243]
  10. Olle Engkvists Stiftelse [204-0256]
  11. EC [GA-955837]
  12. Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [2009-00971]

向作者/读者索取更多资源

Increasing the benzene content to increase the lactone group density can enhance the electron affinity, favoring the doping process, and significantly increasing the electrical conductivity.
Three lactone-based rigid semiconducting polymers were designed to overcome major limitations in the development of n-type organic thermoelectrics, namely electrical conductivity and air stability. Experimental and theoretical investigations demonstrated that increasing the lactone group density by increasing the benzene content from 0 % benzene (P-0), to 50 % (P-50), and 75 % (P-75) resulted in progressively larger electron affinities (up to 4.37 eV), suggesting a more favorable doping process, when employing (N-DMBI) as the dopant. Larger polaron delocalization was also evident, due to the more planarized conformation, which is proposed to lead to a lower hopping energy barrier. As a consequence, the electrical conductivity increased by three orders of magnitude, to achieve values of up to 12 S cm and Power factors of 13.2 mu Wm(-1) K-2 were thereby enabled. These findings present new insights into material design guidelines for the future development of air stable n-type organic thermoelectrics.

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