Perovskite stability and solar conversion performance improve in materials with less bromide migration
Researchers find a way to improve the stability of hybrid organic-inorganic crystals called mixed halide-perovskites, a promising material for solar cells.
DOE/US Department of Energy
The Science
Scientists are interested in improving the stability of a class of crystalline materials that, if more stable, could be the basis for inexpensive solar cells. These materials, called mixed halide-perovskites, combine organic and inorganic materials. The crystals are made of a type of chemical compounds called halides that combine bromides (compounds of bromine) and iodides (compounds of iodine). However, the resulting materials are unstable because of structural defects that arise due to rapid and unequal crystallization when the material forms. These defects enable bromide and iodide to move within the crystal. They move at different rates and separate in ways that reduces the performance of the overall material. Now, researchers have developed a new way to make perovskites. The resulting mixed halide-perovskite film has fewer defects and improved stability.
The Impact
The new method of making mixed halide-perovskites results in solar cells with improved stability and performance. The new method results in better control over perovskite crystallization rates. This means the crystal structure is more ordered, in part due to researchers understanding and taking advantage of the faster crystallization of bromide relative to iodide. The result is a material with fewer defects and less halide migration and thus less segregation of the bromide and iodide. This in turn means uniform mixing of bromide and iodide across the material, which allows the material to absorb light evenly. The end result is that solar cells made using the new method will perform better under real-world conditions.
Summary
Typical halide perovskite solution deposition uses an anti-solvent drip procedure to initiate crystallization of the halide film. The standard anti-solvent method for producing bromide-iodide mixed halide perovskite films often leads to excessive defect formation (e.g., bromide vacancies) owing to the rapid crystallization of bromide vs. iodide-perovskite phases. Simulations show that halide migration is enhanced in the presence of a large population of halide vacancies. This limits the stability of bromide-iodide mixed halide perovskites under light and heat.
In comparison to the anti-solvent approach, the gentler gas-quench method better controls crystallization, first producing a bromide-rich surface layer that then induces top-down columnar growth to form a gradient structure with less bromide in the bulk than in the surface region. The anti-solvent method does not produce such a gradient structure. In this study, researchers from the National Renewable Energy Laboratory, the University of Toledo, and the University of Colorado Boulder demonstrated that the gas-quench method also produces fewer bromide vacancies and results in materials with a higher quality opto-electronic performance. Solar cells made using the gas-quench method retain desirable light absorption properties and provide enhanced performance in the form of a higher charge carrier mobility, higher open circuit voltage, and enhanced stability.
Funding
This research was funded by the Department of Energy (DOE) Office of Science, Office of Basic Energy Sciences, Energy Frontier Research Centers (EFRC) Program. The authors acknowledge the support from the Center for Hybrid Organic Inorganic Semiconductors for Energy (CHOISE), an Energy Frontier Research Center funded by DOE Office of Science, the Office of Basic Energy Sciences. The work on fabrication and testing of solar cells was supported by the Advanced Perovskite Cells and Modules program of the National Center for Photovoltaics, funded by the DOE Office of Energy Efficiency and Renewable Energy, Solar Energy Technologies Office. The first-principles calculations were performed using computational resources sponsored by the DOE Office of Energy Efficiency and Renewable Energy and located at the National Renewable Energy Laboratory.
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