Design principles for water dissociation catalysts in high-performance bipolar membranes

Water dissociation (WD, H2O -> H+ + OH-) is the core process in bipolar membranes (BPMs) that limits energy efficiency. Both electric-field and catalytic effects have been invoked to describe WD, but the interplay of the two and the underlying design principles for WD catalysts remain unclear. Using precise layers of metal-oxide nanoparticles, membrane-electrolyzer platforms, materials characterization, and impedance analysis, we illustrate the role of electronic conductivity in modulating the performance of WD catalysts in the BPM junction through screening and focusing the interfacial electric field and thus electrochemical potential gradients. In contrast, the ionic conductivity of the same layer is not a significant factor in limiting performance. BPM water electrolyzers, optimized via these findings, use -30-nm-diameter anatase TiO2 as an earth-abundant WD catalyst, and generate O-2 and H-2 at 500 mA cm(-2) with a record-low total cell voltage below 2 V. These advanced BPMs might accelerate deployment of new electrodialysis, carbon-capture, and carbon-utilization technology.

Automated summary

This study reveals the important role of electronic conductivity in modulating the performance of water dissociation catalysts in bipolar membranes and finds that ionic conductivity has little effect on performance. Optimized BPM water electrolyzers can efficiently generate oxygen and hydrogen, which may accelerate the deployment of new technologies.