This photo shows strain-engineered, single-crystal thin films of perovskite, which were grown on a series of substrates with varying compositions and lattice sizes. Photo: David Baillot/UC San Diego Jacobs School of Engineering.
This photo shows strain-engineered, single-crystal thin films of perovskite, which were grown on a series of substrates with varying compositions and lattice sizes. Photo: David Baillot/UC San Diego Jacobs School of Engineering.

A new method could allow researchers to fabricate more efficient and longer lasting perovskite solar cells, LEDs and photodetectors. By growing thin perovskite films on substrates with different compositions, engineers at the University of California (UC) San Diego have managed to fabricate perovskite single crystals with precisely deformed, or strained, structures. The engineers report their work in a paper in Nature.

Engineering a small amount of strain in perovskites is of great interest because it provides a way to make significant changes to the material's properties, including to its stability and how it conducts electricity, and absorbs and transmits light.

"You can use strain engineering as a knob to tune existing functions or even install new functions in a material," said Sheng Xu, a professor of nanoengineering at the UC San Diego Jacobs School of Engineering and senior author of the paper.

There are techniques that use heat to introduce strain into perovskite crystals, but this strain is typically short lived or uncontrollable in terms of its magnitude, making these strain-engineered perovskites impractical to use. Existing strain engineering techniques are also incompatible with current device fabrication processes.

Xu and his team tackled these problems by carefully growing deformed perovskite single crystals. Their technique permanently embeds strain into the material's structure and allows the amount of strain to be tailored – the more deformed the crystal lattice, the higher the strain.

The type of perovskite investigated in this study is known as alpha-formamidinium lead iodide, which has been used to create the highest efficiency perovskite solar cells to date. The researchers grew crystals of this material on a series of perovskite substrates with varying compositions and lattice sizes – a process called heteroepitaxial growth. As the material crystallized, it adopted the lattice size of its substrate, which essentially forced the alpha-formamidinium lead iodide crystals to grow differently than they normally do.

"Thus, the lattices in the material are deformed and strained to different degrees, depending on the lattice mismatch between material and substrate," explained Yimu Chen, a nanoengineering PhD student in Xu's lab and co-first author of the paper.

"Because we are introducing strain at the atomic level, we can precisely design the strain and control it," added Yusheng Lei, also a nanoengineering PhD student in Xu's lab and the other co-first author of the paper.

The researchers grew perovskite crystals with five different levels of strain, ranging from 0 to -2.4%. They found that -1.2% strain produced samples with the best charge-carrier mobility.

The team also reported another interesting discovery: growing alpha-formamidinium lead iodide crystals with strain helped to stabilize its photoactive alpha phase. "In its strain-free form, alpha-formamidinium lead iodide undergoes a phase transition from a photoactive phase to a non-photoactive phase, which is bad for photovoltaic applications," Chen said. "With our growth method, we can lock the material's crystal structure with that of the substrate to prevent this phase transition and enhance its phase stability."

In future studies, the researchers will explore what new properties and functionalities they can strain engineer into perovskites using their method. They will also work on scaling up their process to grow large, single-crystalline thin films for industrial applications.

This story is adapted from material from the University of California San Diego, with editorial changes made by Materials Today. The views expressed in this article do not necessarily represent those of Elsevier. Link to original source.