4.5 Article

The Effect of Oligo(Ethylene Oxide) Side Chains: A Strategy to Improve Contrast and Switching Speed in Electrochromic Polymers

Journal

CHEMPHYSCHEM
Volume 21, Issue 4, Pages 321-327

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.201901047

Keywords

affinity; oligo(ethylene oxide) chains; electrochromic polymers; switching speed; thieno[3; 2-b]thiophene

Funding

  1. National Natural Science Foundation of China [51873002, 51803005, 51761145101]
  2. Key-Area Research and Development Program of Guangdong Province [2019B010924003]
  3. Guangdong International Collaborative Research Center for Optoelectronic Materials and Devices [2019 A050505003]
  4. Shenzhen Peacock Plan [KQTD2014062714543296]
  5. Shenzhen Engineering Laboratory (Shenzhen Development and Reform Commission) [[2016]1592]
  6. Shenzhen Science and Technology Innovation Commission [JCYJ20170818085725139, JCYJ20170818090312652, JCYJ20180302150354741]

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Solution-processable electrochromic polymers (ECPs) with high performance are urgently needed for extensive applications. Nevertheless, they suffer from slow switching speed because of low ionic conductivities. Herein, we present an effective strategy to improve the contrast and switching speed in ECPs via facile side-chain engineering. A novel electrochromic thieno[3,2-b]thiophene-based polymer (PmOTTBTD) is designed and successfully synthesized by introducing oligo(ethylene oxide) side chains with high ionic conductivity. Compared to the counterpart POTTBTD without modification by oligo(ethylene oxide) chains, PmOTTBTD demonstrates nearly double contrast (42 % vs. 24 %) with a fast oxidation switching process that just takes half of the time when detected under 400 nm, as well as much higher coloration efficiencies (e. g. 239.04 cm(2) C-1 vs. 226.26 cm(2) C-1 @ 400 nm and 314.04 cm(2) C-1 vs. 174.00 cm(2) C-1 @ 650 similar to 700 nm). Besides, PmOTTBTD exhibits excellent stability with negligible decay after 3000 cycles. Our work suggests a facile strategy that could be adopted to realize high-performance ECPs via molecular design tuning.

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