Chemistry Seminar Presented by Prof. Shannon Boettcher "The Chemistry and Physics of Bipolar Membranes with Applications in Water, Energy, and Decarbonization"

March 26, -
Speaker(s): Shannon Boettcher, University of California, Berkeley
The Department of Chemistry is excited to host Shannon Boettcher (University of California, Berkeley)

The Chemistry and Physics of Bipolar Membranes
with Applications in Water, Energy, and Decarbonization

Prof. Shannon Boettcher
Department of Chemistry and Biochemistry and the Materials Science Institute
Director, Oregon Center for Electrochemistry

Bipolar membranes (BPMs) are ionic analogues of semiconductor pn junctions and consist of an anion-selective ionomer membrane laminated with a cation-selective ionomer membrane. BPMs generate pH gradients under bias by driving water dissociation (WD) into protons and hydroxide at the interface between the two different ionomers. In BPM water electrolysis, this feature enables devices that drive proton reduction in locally acidic conditions, where electrode kinetics are fast, and water oxidation in locally basic conditions where efficient earth-abundant catalysts are stable. In electrodialysis, BPMs generate acid and base from salt water on demand for wastewater treatment/reuse, CO2 capture from the air or ocean, and niche applications like food/drink processing. As the predominant H+/OH- ion flow is out from the center of the BPM, in electrosynthesis BPMs mitigate deleterious cross-over of reactants and products.
The key factor traditionally limiting the use of BPMs to niche applications, has been the low operating currents and high voltage losses (~0.4 V at 0.1 A/cm2). We have isolated the voltage loss in BPMs to kinetics of the water dissociation (WD) reaction, nominally H2O → H+ + OH-. We invented physical electrochemical platforms to study the basic factors and mechanisms that control the kinetics of WD, discovering how tuned metal-oxide nanoparticles provide surfaces with (controllable) proton-absorption sites that catalyze WD while also focusing the interfacial electric field across the BPM junction and thus further speeding the WD rate (e.g. Science 2020, Nature Comm. 2022). Temperature-dependent measurements show the WD catalysts do not primarily lower the activation energy for WD, but instead dramatically increase the number of water configurational microstates poised for the proton-transfer elementary steps in WD (Joule, 2023). These discoveries enable design of new WD catalysts for BPMs that operate with 40-times better voltage efficiency than the commercial state of the art, and at current-densities of up to 4 A/cm2, opening tremendous new application space.