BESSY II: What drives ions through polymer membranes

Membrane.

Membrane. © HZB

Photoelectrolysers and electrolysis cells can produce green hydrogen or fossil-free carbon compounds – but they require ion-exchange membranes. An HZB team has now studied the transport of ions through the membrane in a hybrid liquid gas electrolyzer at the X-ray source BESSY II. Contrary to expectations, however, concentration differences hardly drive electric field ions. Diffusion is therefore the decisive process. This finding could help in the development of highly efficient and significantly more environmentally friendly membrane materials.

Ion exchange membranes are needed in (photo)electrolysers, fuel cells and batteries to separate ions and enable the desired processes. Polymeric membranes such as synthetically produced compounds like NAFION are particularly efficient, but they cannot be degraded. A ban on the use of these “eternal chemicals” is currently under discussion in the European Union. The development of suitable alternatives will be a major challenge. So, it is crucial to understand why NAFION and other established polymeric membranes work so well.

A team led by Dr. Marco Favaro of the HZB Institute for Solar Fuels has now investigated this using a special type of electrolysis cell. Here, the membrane sits on the outer wall and is in contact with both the liquid electrolyte and a gaseous external environment. It can act either as an anode or a cathode, depending on the polarity of the applied potential. This hybrid liquid-gas electrolyzer is considered particularly favorable for the electrochemical conversion of CO2. This is thanks to the higher CO2 concentrations that can be achieved in the gas phase. Thereby overcoming the poor solubility of CO2 in aqueous solutions.

For the study, Favaro and his team used commercially available ion-exchange membranes in contact with a model electrolyte like sodium chloride (NaCl) in water. Water vapor was fed to the gas phase, with the partial pressure of water close to its vapor pressure at room temperature. To analyze the migration of sodium and chloride ions through the membrane, they used in situ ambient pressure hard X-ray photoelectron spectroscopy (AP-HAXPES) at the SpAnTeX end-station at the KMC-1 beamline of BESSY II.

Ion exchange membranes are key component

“Indeed, we were expecting that the ion dynamics was determined, under applied potentials, by the electric fields generated between the anode and cathode of the electrolyzer, and that electromigration was therefore the main driver,” says Marco Favaro.

However, analysis of the data showed otherwise. Electromigration hardly plays a role. The ions simply diffuse across the membrane. The data could be perfectly simulated numerically with a diffusion model. “Our conclusion is that ions move through the polymer membranes in these types of electrolyzers due to hopping mediated by the ionized functional groups present in the membranes. In addition, since water diffuses as well through the polymer, the ions are “dragged” as well” explains Favaro.

These results are exciting for a number of reasons. These types of electrolyzers are a way to convert CO2 into valuable chemicals that can otherwise only be obtained from fossil fuels. Understanding how these devices work helps on the way to decarbonize the economy. On the other hand, the ion-exchange membranes that are a key component of these cells are themselves problematic. The European Union may soon ban the use of persistent chemicals. Understanding the relevant drivers of such transport processes will help to develop new membrane materials that are both efficient, durable, and environmentally friendly. Favaro now intends to take this project forward at HIPOLE. The new Helmholtz Institute in Jena, which will focus on polymer materials for new energy technologies.

arö

  • Copy link

You might also be interested in

  • Battery research: visualisation of aging processes operando
    Science Highlight
    29.04.2025
    Battery research: visualisation of aging processes operando
    Lithium button cells with electrodes made of nickel-manganese-cobalt oxides (NMC) are very powerful. Unfortunately, their capacity decreases over time. Now, for the first time, a team has used a non-destructive method to observe how the elemental composition of the individual layers in a button cell changes during charging cycles. The study, now published in the journal Small, involved teams from the Physikalisch-Technische Bundesanstalt (PTB), the University of Münster, researchers from the SyncLab research group at HZB and the BLiX laboratory at the Technical University of Berlin. Measurements were carried out in the BLiX laboratory and at the BESSY II synchrotron radiation source.
  • New instrument at BESSY II: The OÆSE endstation in EMIL
    Science Highlight
    23.04.2025
    New instrument at BESSY II: The OÆSE endstation in EMIL
    A new instrument is now available at BESSY II for investigating catalyst materials, battery electrodes and other energy devices under operating conditions: the Operando Absorption and Emission Spectroscopy on EMIL (OÆSE) endstation in the Energy Materials In-situ Laboratory Berlin (EMIL). A team led by Raul Garcia-Diez and Marcus Bär showcases the instrument’s capabilities via a proof-of-concept study on electrodeposited copper.
  • Green hydrogen: A cage structured material transforms into a performant catalyst
    Science Highlight
    17.04.2025
    Green hydrogen: A cage structured material transforms into a performant catalyst
    Clathrates are characterised by a complex cage structure that provides space for guest ions too. Now, for the first time, a team has investigated the suitability of clathrates as catalysts for electrolytic hydrogen production with impressive results: the clathrate sample was even more efficient and robust than currently used nickel-based catalysts. They also found a reason for this enhanced performance. Measurements at BESSY II showed that the clathrates undergo structural changes during the catalytic reaction: the three-dimensional cage structure decays into ultra-thin nanosheets that allow maximum contact with active catalytic centres. The study has been published in the journal ‘Angewandte Chemie’.