The central challenge with chloride-ion batteries has been movement. Chloride ions have not historically travelled through solid materials as efficiently as lithium ions, limiting their potential in practical battery systems. For chloride-based batteries to become viable, the ions need a clearer and faster pathway through the solid electrolyte.
Researchers led by Sarbajit Banerjee, professor at ETH Zürich and head of the Laboratory for Battery Science at Switzerland’s Paul Scherrer Institute, worked with PhD student Jingxiang Cheng to modify lanthanum oxychloride, a solid material capable of conducting chloride ions.
The team introduced small amounts of calcium, magnesium or strontium into the material’s atomic structure. Calcium produced the strongest result, helping chloride ions move up to 10,000 times faster. Instead of pushing large ions through a rigid structure, the modified material became more flexible at the atomic level, improving the pathway for ion transport.
The Canadian Light Source helped explain what changed inside the material. Using ultrabright X-rays, including work at the VLS-PGM beamline, the researchers examined how the added elements affected the structure. The findings showed that a more flexible framework can allow chloride ions to move more freely through a solid electrolyte.
The results, published in ACS Applied Energy Materials, add to early research into halide-ion battery systems. Commercial deployment is not around the corner, and chloride-based solid-state batteries will need significant development before they can be tested in real-world grid projects.
Even so, the research is relevant for the business of energy storage. As renewable generation grows, grid operators will need technologies that fit different durations, locations, cost profiles and supply chains. Chloride-based batteries may not be a near-term solution, but they could become part of a broader shift toward storage systems built from more abundant materials.