The increasing share of renewables in electric grids nowadays causes a growing daily and seasonal mismatch between electricity generation and demand. In this regard, novel energy storage systems need to be developed, to allow large-scale storage of the excess electricity during low-demand time, and its distribution during peak demand time. Acid–base flow battery (ABFB) is a novel and environmentally friendly technology based on the reversible water dissociation by bipolar membranes, and it stores electricity in the form of chemical energy in acid and base solutions. The technology has already been demonstrated at the laboratory scale, and the experimental testing of the first 1 kW pilot plant is currently ongoing. This work aims to describe the current development and the perspectives of the ABFB technology. In particular, we discuss the main technical challenges related to the development of battery components (membranes, electrolyte solutions, and stack design), as well as simulated scenarios, to demonstrate the technology at the kW–MW scale. Finally, we present an economic analysis for a first 100 kW commercial unit and suggest future directions for further technology scale-up and commercial deployment.
Bipolar membranes (BPMs), a special class of ion exchange
membranes
with the unique ability to electrochemically induce either water dissociation
or recombination, are of growing interest for environmental applications
including eliminating chemical dosage for pH adjustment, resource
recovery, valorization of brines, and carbon capture. However, ion
transport within BPMs, and particularly at its junction, has remained
poorly understood. This work aims to theoretically and experimentally
investigate ion transport in BPMs under both reverse and forward bias
operation modes, taking into account the production or recombination
of H+ and OH–, as well as the transport
of salt ions (e.g., Na+, Cl–) inside
the membrane. We adopt a model based on the Nernst–Planck theory,
that requires only three input parametersmembrane thickness,
its charge density, and pK of proton adsorptionto
predict the concentration profiles of four ions (H+, OH–, Na+, and Cl–) inside
the membrane and the resulting current–voltage curve. The model
can predict most of the experimental results measured with a commercial
BPM, including the observation of limiting and overlimiting currents,
which emerge due to particular concentration profiles that develop
inside the BPM. This work provides new insights into the physical
phenomena in BPMs and helps identify optimal operating conditions
for future environmental applications.
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