As researchers push the boundaries of battery design, seeking to pack ever greater amounts of power and energy into a given amount of space or weight, one of the more promising technologies being studied is lithium-ion batteries that use a solid electrolyte material between the two electrodes, rather than the typical liquid. But such batteries have been plagued by a tendency for branch-like projections of metal called dendrites to form on one of the electrodes, eventually bridging the electrolyte and shorting out the battery cell.

Researchers have found a way to prevent such dendrite formation, potentially unleashing the potential of this new type of high-powered battery. Solid-state batteries have been a long-sought technology for two reasons: safety and energy density. But the only way to reach the energy densities that are interesting is to use a metal electrode. And while it’s possible to couple that metal electrode with a liquid electrolyte and still get good energy density, that does not provide the same safety advantage as a solid electrolyte does.

Solid-state batteries only make sense with metal electrodes but attempts to develop such batteries have been hampered by the growth of dendrites, which eventually bridge the gap between the two electrode plates and short out the circuit, weakening or inactivating that cell in a battery.

Dendrites form more rapidly when the current flow is higher — which is generally desirable in order to allow rapid charging. So far, the current densities that have been achieved in experimental solid-state batteries have been far short of what would be needed for a practical commercial rechargeable battery. But the promise is worth pursuing because the amount of energy that can be stored in experimental versions of such cells is already nearly double that of conventional lithium-ion batteries.

The team solved the dendrite problem by adopting a compromise between solid and liquid states. They made a semisolid electrode in contact with a solid electrolyte material. The semisolid electrode provided a kind of self-healing surface at the interface, rather than the brittle surface of a solid that could lead to tiny cracks that provide the initial seeds for dendrite formation.

The idea was inspired by experimental high-temperature batteries, in which one or both electrodes consist of molten metal. The hundreds-of-degrees temperatures of molten-metal batteries would never be practical for a portable device but the work demonstrated that a liquid interface can enable high current densities with no dendrite formation. The material is more solid than liquid but resembles the amalgam dentists use to fill a cavity — solid metal but still able to flow and be shaped. At the ordinary temperatures that the battery operates in, it stays in a regime where there is both a solid phase and a liquid phase — in this case made of a mixture of sodium and potassium.

The arrow points to the branch-like dendrite formations on the electrode. (Credit: Courtesy of the researchers)

The team demonstrated that it was possible to run the system at 20 times greater current than using solid lithium, without forming any dendrites. The next step was to replicate that performance with an actual lithium-containing electrode.

In a second version of the solid battery, the team introduced a very thin layer of liquid sodium potassium alloy in between a solid lithium electrode and a solid electrolyte. They showed that this approach could also overcome the dendrite problem, providing an alternative approach for further research.

The new approaches could easily be adapted to many different versions of solid-state lithium batteries that are being investigated. The team’s next step will be to demonstrate this system’s applicability to a variety of battery architectures. The technology could be used immediately in cell development for a wide range of applications, from handheld devices to electric vehicles to electric aviation.

For more information, contact Abby Abazorius at This email address is being protected from spambots. You need JavaScript enabled to view it.; 617-253-2709.