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Updated: Sep 20, 2025

Probing and Mapping Electrode Surfaces in Solid Oxide Fuel Cells
Published on: September 20, 2012
Nanocomposites from Polymer Brushes and Metal Oxide Clusters for Fabrication of High-Temperature Fuel Cell Proton
Lu Liu1, Jiayi Huang1, Mingxin Zhang2
1State Key Laboratory of Luminescent Materials and Devices & South China Advanced Institute for Soft Matter Science and Technology, Guangdong Basic Research Center of Excellence for Energy and Information Polymer Materials, South China University of Technology, Guangzhou, 510641, P. R. China.
Abstract:
High-temperature proton exchange membranes (HT-PEMs) are highly desired for fuel cells with high energy density; however, the requirements in balanced anhydrous proton conductivity, mechanical/structural stability, processability and gas-barrier property impose great difficulty for molecular design. Herein, the supramolecular complexation of brush polymers and super acidic metal oxide cluster (H3PW12O40, abbreviation PW12) affords HT-PEMs with comprehensive performance that contributes to the robust performance of high energy density fuel cells. The polymers brush topology enables the decoupling of mechanical properties and proton conduction: the polyethylene glycol (PEG) side chains possess high affinity to PW12 for proton transport while the rigid backbones help maintain structural stability and mechanical strengths up to 250 °C. The PW12 clusters can be homogeneously dispersed in PEG with high loadings (≈80 wt.%) and it facilitates proton hopping among the crowded PW12 for promising anhydrous proton conduction, e.g., 2 × 10-3 S cm-1 at 200 °C. Their dense supramolecular bonds contribute to enhanced mechanical strength, flexibility and gas barrier property with mitigating hydrogen permeation current as 0.73 mA cm-2, enabling the feasible processability of PEMs and stable operation of fuel cells. The devices show high power density as 218 mW cm-2 at 180 °C with long-term stable operation.

