4.6 Article

Chemical Vapor Deposition Synthesis of Tunable Unsubstituted Polythiophene

Journal

LANGMUIR
Volume 27, Issue 24, Pages 15223-15229

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la203318f

Keywords

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Funding

  1. NSF [CBET-0846245]
  2. NSF SGER [CBET-0820608]
  3. ACS PRF [48160-GS]
  4. NSF MRI-R2 [CBET-0959361]
  5. Directorate For Engineering
  6. Div Of Chem, Bioeng, Env, & Transp Sys [0846245] Funding Source: National Science Foundation
  7. Div Of Chem, Bioeng, Env, & Transp Sys
  8. Directorate For Engineering [0959361] Funding Source: National Science Foundation

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Despite having exceptional electroactive properties, applications of unsubstituted polythiophene (PTh) have been limited due to its insolubility. To overcome this challenge, we have employed oxidative chemical vapor deposition (oCVD) as a unique liquid-free technique to enable the oxidative polymerization of PTh using thiophene as the starting monomer and vanadium oxytrichloride as an effective vaporizable oxidant initiator. Vibrational and phototelectron spectroscopy indicated the formation of unsubstituted polythiophene. Cyclic voltammetry revealed its electrochromic behavior in solution. Significantly, polymer conjugation length and electrical conductivity can be tuned by controlling oCVD process variables. Polymerization is found to be adsorption-limited, so by providing sufficient monomer and limiting the amount of initiator at the growth surface, PTh is believed to be formed through alpha-alpha a thiophene linkages.

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