The current crop of battery technology seems unable to keep up with the increasing demands we are placing on our ever-growing collection of mobile devices. Which is why research into next generation battery technology is such a focus around the world. A new high-performance anode structure based on silicon-carbon composite materials could significantly improve the performance of lithium-ion batteries used in our portable electronics and gaining widespread use in electric and hybrid vehicles.
Produced with a “bottom-up” self-assembly technique, the new high-performance anode structure developed by researchers at the Georgia Institute of Technology takes advantage of nanotechnology to fine-tune its materials properties, addressing the shortcomings of earlier silicon-based battery anodes.
Graphite anodes use particles ranging in size from 15 to 20 microns. If silicon particles of that size are simply substituted for the graphite, expansion and contraction as the lithium ions enter and leave the silicon creates cracks that quickly cause the anode to fail.
The new nanocomposite material solves that degradation problem, potentially allowing battery designers to tap the capacity advantages of silicon. That could facilitate higher power output from a given battery size – or allow a smaller battery to produce a required amount of power.
Electrical measurements of the new composite anodes in small coin cells showed they had a capacity more than five times greater than the theoretical capacity of graphite.
Using graphitic carbon as an electrically-conductive binder, the silicon-carbon composites are then self-assembled into rigid spheres that have open, interconnected internal pore channels. The spheres, formed in sizes ranging from 10 to 30 microns, are used to form battery anodes. The relatively large composite powder size – a thousand times larger than individual silicon nanoparticles – allows easy powder processing for anode fabrication.
The internal channels in the silicon-carbon spheres serve two purposes. They admit liquid electrolyte to allow rapid entry of lithium ions for quick battery charging, and they provide space to accommodate expansion and contraction of the silicon without cracking the anode. The internal channels and nanometer-scale particles also provide short lithium diffusion paths into the anode, boosting battery power characteristics.
The size of the silicon particles is controlled by the duration of the chemical vapor deposition process and the pressure applied to the deposition system. The size of the carbon nanostructure branches and the size of the silicon spheres determine the pore size in the composite.
And because the final composite spheres are relatively large when they are fabricated into anodes, the self-assembly technique avoids the potential health risks of handling nanoscale powders.
So far, the researchers have tested the new anode through more than a hundred charge-discharge cycles. Gleb Yushin, an assistant professor in the School of Materials Science and Engineering at the Georgia Institute of Technology, believes the material would remain stable for thousands of cycles because no degradation mechanisms have become apparent.
“If this technology can offer a lower cost on a capacity basis, or lighter weight compared to current techniques, this will help advance the market for lithium batteries,” he said. “If we are able to produce less expensive batteries that last for a long time, this could also facilitate the adoption of many ‘green’ technologies, such as electric vehicles or solar cells.”
A paper detailing the new high-performance anode appears in the March 14, 2010 issue of the journal Nature Materials.
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