Investigation of Ionomer and Catalyst (Co3O4, Mn3O4, or MnO2) Interactions Using a Polyethylene Midblock Copolymer in Anion Exchange Water Electrolyzers to Understand Performance and Durability

Author:

Kim ChulOongORCID,Salgado Marco J.ORCID,Hawks Jordan L.ORCID,Creel Jack W.ORCID,Dunn Kevin C.ORCID,Beiler Kaylee J.ORCID,Wu IvyORCID,Kuo Mei-ChenORCID,Herring Andrew M.ORCID

Abstract

An anion exchange membrane water electrolyzer (AEMWE) was studied with three electrocatalysts (Co3O4, Mn2O3, MnO2) for the oxygen evolution reactions at 50 °C in 1 M K2CO3(aq). We employ an optimized robust high performance polymer based on a polyethylene mid-block copolymer, poly(vinylbenzyl-N‑methylpiperidinium carbonate)‑b‑polyethylene‑b‑poly(vinylbenzyl-N‑methylpiperidinium carbonate) as the AEM and the anode ionomer. The cathode utilized a high loading of Pt/C, 1 mg cm−2, to minimize contributions to the kinetics. We tested three catalyst loadings (0.5, 2.5, and 4.5 mg cm−2) with a fixed ionomer loading of 0.5 mg cm−2 to assess ionomer-catalyst interactions. The best-performing catalyst loadings were investigated in a 100 h durability test at 750 mA cm−2. The 2.5 mg cm−2 MnO2 catalyst displayed superior performance, with 2.40 ± 0.02 V at 1 A cm−2. In the 100 h durability test, the Mn2O3 catalyst showed a degradation rate of +269 ± 15 μV h−1, whereas Co3O4 and MnO2 showed −800 ± 157 μV h−1, −114 ± 15 μV h−1, respectively with no membrane thinning indicating a gradual improvement. The MnO2 electrode was further investigated in a 500 h test was conducted, revealing a voltage change rate of −21 μV h−1 for 24–375 h. Pre and post-test FTIR mapping revealed evolution of micrometer-sized morphology corresponding to templating by the Ni-foam electrode.

Funder

Colorado Office of Economic Development and International Trade

Army Research Office

Publisher

The Electrochemical Society

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