Defects in next-generation solar cells can be healed with light

The concoction of light with water and oxygen molecules leads to substantial defect-healing in metal halide perovskite semiconductors. Credit: Dr. Matthew T. Klug

Researchers have shown that defects in the molecular structure of perovskites - a material which could revolutionise the solar cell industry - can be "healed" by exposing it to light and just the right amount of humidity.

The international team of researchers demonstrated in 2016 that defects in the of perovskites could be healed by exposing them to light, but the effects were temporary.

Now, an expanded team, from Cambridge, MIT, Oxford, Bath and Delft, have shown that these defects can be permanently healed, which could further accelerate the development of cheap, high-performance perovskite-based that rival the efficiency of silicon. Their results are reported in the inaugural edition of the journal Joule, published by Cell Press.

Most solar cells on the market today are silicon-based, but since they are expensive and energy-intensive to produce, researchers have been searching for alternative materials for solar cells and other photovoltaics. Perovskites are perhaps the most promising of these alternatives: they are cheap and easy to produce, and in just a few short years of development, perovskites have become almost as efficient as silicon at converting sunlight into electricity.

Despite the potential of perovskites, some limitations have hampered their efficiency and consistency. Tiny defects in the crystalline structure of perovskites, called traps, can cause electrons to get "stuck" before their energy can be harnessed. The easier that electrons can move around in a , the more efficient that material will be at converting photons, particles of light, into electricity.

"In perovskite solar cells and LEDs, you tend to lose a lot of efficiency through defects," said Dr Sam Stranks, who led the research while he was a Marie Curie Fellow jointly at MIT and Cambridge. "We want to know the origins of the defects so that we can eliminate them and make perovskites more efficient."

In a 2016 paper, Stranks and his colleagues found that when perovskites were exposed to illumination, iodide ions - atoms stripped of an electron so that they carry an electric charge - migrated away from the illuminated region, and in the process swept away most of the defects in that region along with them. However, these effects, while promising, were temporary because the ions migrated back to similar positions when the light was removed.

In the new study, the team made a perovskite-based device, printed using techniques compatible with scalable roll-to-roll processes, but before the device was completed, they exposed it to light, oxygen and . Perovskites often start to degrade when exposed to humidity, but the team found that when humidity levels were between 40 and 50 percent, and the exposure was limited to 30 minutes, degradation did not occur. Once the exposure was complete, the remaining layers were deposited to finish the device.

When the light was applied, electrons bound with oxygen, forming a superoxide that could very effectively bind to electron traps and prevent these traps from hindering electrons. In the accompanying presence of water, the surface also gets converted to a protective shell. The shell coating removes traps from the surfaces but also locks in the superoxide, meaning that the performance improvements in the perovskites are now long-lived.

"It's counter-intuitive, but applying humidity and makes the more luminescent, a property which is extremely important if you want efficient solar ," said Stranks, who is now based at Cambridge's Cavendish Laboratory. "We've seen an increase in luminescence efficiency from one percent to 89 percent, and we think we could get it all the way to 100 percent, which means we could have no voltage loss - but there's still a lot of work to be done."

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More information: Metal Halide Perovskite Polycrystalline Films Exhibiting Properties of Single Crystals, Joule, DOI: 10.1016/j.joule.2017.08.006

Provided by University of Cambridge