Prof. Shannon Boettcher

Chemical and Biomolecular Engineering and Chemistry

University of California, Berkeley

Senior Scientist and Deputy Director

   Energy Storage & Distributed Resources Division

   Lawrence Berkeley National Laboratory

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 applications of BPMs 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 to speed 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 enabled the design of new WD catalysts for BPMs that operate with 40-times better voltage efficiency than the commercial state of the art (Nature Materials, 2024), and at current-densities of up to 4 A/cm², driving commercialization efforts and new application space particularly for high-current electrodialysis (ACS Energy Letters, 2025).

Biography: Boettcher is the Vermeulen Professor in Departments of Chemical Engineering and Chemistry at the University of California, Berkeley, and the Deputy Director of the Energy Storage and Distributed Resources Division at Lawrence Berkeley National Laboratory. His research is at the intersection of electrochemistry, materials science, and device engineering, with a focus on fundamental and applied aspects of energy conversion and storage. In 2023 he was the Blavatnik National Award Laureate in Chemistry. In 2019 he founded the Oregon Center for Electrochemistry and the first graduate program in Electrochemical Technology in the USA, and launched CESET in 2024, the Center for Electrochemical Science, Engineering, and Technology, in Berkeley.