The immobilisation and reactivity of Fe(CN)63−/4− in an intrinsically microporous polyamine (PIM-EA-TB)

Protonation of the molecularly rigid polymer of intrinsic microporosity PIM-EA-TB can be coupled to immobilisation of Fe(CN)₆^3−/4− (as well as immobilisation of Prussian blue) into 1–2 nm diameter channels. The resulting films provide redox-active coatings on glassy carbon electrodes. Uptake, transport, and retention of Fe(CN)₆^3−/4− in the microporous polymer are strongly pH dependent requiring protonation of the PIM-EA-TB (pK_A ≈ 4). Both Fe(CN)₆⁴⁻ and Fe(CN)₆³⁻ can be immobilised, but Fe(CN)₆⁴⁻ appears to bind tighter to the polymer backbone presumably via bridging protons. Loss of Fe(CN)₆^3−/4− by leaching into the aqueous solution phase becomes significant only at pH > 9 and is likely to be associated with hydroxide anions directly entering the microporous structure to combine with protons. This and the interaction of Fe(CN)₆^3−/4− and protons within the molecularly rigid PIM-EA-TB host are suggested to be responsible for retention and relatively slow leaching processes. Electrocatalysis with immobilised Fe(CN)₆^3−/4− is demonstrated for the oxidation of ascorbic acid.

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Acid–Base Interaction Enhancing Oxygen Tolerance in Electrocatalytic Carbon Dioxide Reduction

Hybrid electrodes with improved O₂ tolerance and capability of CO₂ conversion into liquid products in the presence of O₂ are presented. Aniline molecules are introduced into the pore structure of a polymer of intrinsic microporosity to expand its gas separation functionality beyond pure physical sieving. The chemical interaction between the acidic CO₂ molecule and the basic amino group of aniline renders enhanced CO₂ separation from O₂. Loaded with a cobalt phthalocyanine-based cathode catalyst, the hybrid electrode achieves a CO Faradaic efficiency of 71 % with 10 % O₂ in the CO₂ feed gas. The electrode can still produce CO at an O₂/CO₂ ratio as high as 9:1. Switching to a Sn-based catalyst, for the first time O₂-tolerant CO₂ electroreduction to liquid products is realized, generating formate with nearly 100 % selectivity and a current density of 56.7 mA cm⁻² in the presence of 5 % O₂.     

Redox reactivity at silver microparticle—glassy carbon contacts under a coating of polymer of intrinsic microporosity (PIM)

Silver microparticles (ca. 1 μm average size clustered into cage-like aggregates of 10–20 μm diameter) are shown to adhere to a glassy carbon electrode surface to give voltammetric current responses, which are considerably enhanced/stabilised when applying a coating with a molecularly rigid polymer of intrinsic microporosity (PIM-EA-TB). In preliminary voltammetric experiments characteristic Ag(0/I) surface oxidation and back-reduction processes are observed in aqueous phosphate buffer (associated with silver phosphate layer formation on the silver surface). In contrast to the oxidation, which is dominated by a nucleation process causing a sharp well-defined current signal, for the back-reduction stochastic current responses are observed possibly associated with density fluctuations in the surrounding liquid phase (“Brownian activation”) as an essential part of the mechanism of conversion of surface-oxidised silver back to silver metal.

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