Interplaying Intrinsic and Extrinsic Proton Conductivities in Covalent Organic Frameworks

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Suman Chandra - , CSIR - National Institute for Interdisciplinary Science and Technology, Academy of Scientific and Innovative Research (Autor:in)
  • Tanay Kundu - , CSIR - National Institute for Interdisciplinary Science and Technology, Academy of Scientific and Innovative Research (Autor:in)
  • Kaushik Dey - , CSIR - National Institute for Interdisciplinary Science and Technology, Academy of Scientific and Innovative Research (Autor:in)
  • Matthew Addicoat - , Jacobs University Bremen (Autor:in)
  • Thomas Heine - , Jacobs University Bremen (Autor:in)
  • Rahul Banerjee - , CSIR - National Institute for Interdisciplinary Science and Technology, Academy of Scientific and Innovative Research (Autor:in)

Abstract

A sulfonic-acid-based covalent organic framework (TpPa-SO3H) has been synthesized that exhibits intrinsic proton conductivity under anhydrous conditions. The sulfonic acid groups are aligned on the two-dimensional (2D) layers at periodic intervals and promote the proton hopping inside the hexagonal one-dimensional channel. The intrinsic proton conductivity of TpPa-SO3H was measured as 1.7 × 10-5 S cm-1 at 120°C under anhydrous conditions. To enhance the proton conductivity, we have synthesized a hybrid COF TpPa-(SO3H-Py) by a ligand-based solid-solution approach that contains sulfonic acid as the acidic site, as well as pyridine as the basic site, in order to immobilize acidic proton carrier molecules. Impregnation of phytic acid molecules inside the framework increases the anhydrous proton conductivity up to 5 × 10-4 S cm-1 at 120°C. Such an approach highlights the advantage and first-time use of hybrid COF for interplaying intrinsic to extrinsic proton conductivity.

Details

OriginalspracheEnglisch
Seiten (von - bis)1489-1494
Seitenumfang6
FachzeitschriftChemistry of materials
Jahrgang28
Ausgabenummer5
PublikationsstatusVeröffentlicht - 8 März 2016
Peer-Review-StatusJa
Extern publiziertJa