4.7 Article

Improving the thermoelectric performances of polymer via synchronously realizing of chemical doping and side-chain cleavage

期刊

CHEMICAL ENGINEERING JOURNAL
卷 429, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.132354

关键词

Side-chain cleavage; Benzodithiophene; Polymer thermoelectrics; P-doping; Interfacial engineering

资金

  1. National Natural Science Foundation of China [51973120]
  2. Natural Science Foundation of Guangdong Province [2019A1515010613]
  3. Instrumental Analysis Center of Shenzhen University (Xili Campus)

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This study designed and synthesized a series of p-type polymer semiconductors containing ester-cleavage groups, which can be degraded in the presence of FeCl3, leading to a significant improvement in electrical conductivity. Increasing crystalline domains through side-chain cleavage contributed to the formation of a (bi)polaron network and further optimized the power factor, enhancing the doping efficiency of the materials.
Side-chain cleavage is an effective strategy to reconstruct the arrangement of polymer main chains, thus improving their electrical properties and corrosion stability. However, simultaneously realizing side-chain cleavage and chemical doping of polymer semiconductors have not been reported. Herein, a series of p-type polymer semiconductors with the incorporation of ester-cleavage groups (PBDTTT-TETx, X is the molar ratio of the cleavage ester groups and nondegradable alkyl groups) were designed and synthesized. The introduced functional ester side-chains on PBDTTT-TET0.5 can be degraded by a commonly used p-type dopant FeCl3 readily, resulting in the maximum 120-fold enhancement in electrical conductivity and 15-fold increase in power factor at the FeCl3 concentration of 30 mM, compared to the reference one (PBDTTT-PET0.5 with the nondegradable ester side-chains). Scanning electron microscopy, atomic force microscopy measurements and X-ray diffraction reveal that the increase of crystalline domains along with the side-chain cleavage contributes to the formation of (bi)polaron network. The improved doping efficiency can be reflected by their ultraviolet photoelectron spectroscopy and UV-vis-NIR spectroscopy results. Moreover, a further optimized power factor can be achieved for PBDTTT-TET0.05, which is 5.8 times higher than that of PBDTTT-TET. Therefore, molecule design strategy by incorporating FeCl3-cleavage ester groups into the pi-conjugated backbones provided an effective approach to establish advanced TE materials.

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