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Highly ordered lead-free double perovskite halides by design
- Source :
- Journal of Materiomics, Vol 6, Iss 4, Pp 651-660 (2020)
- Publication Year :
- 2020
- Publisher :
- arXiv, 2020.
-
Abstract
- Lead-free double perovskite halides are emerging optoelectronic materials that are alternatives to lead-based perovskite halides. Recently, single-crystalline double perovskite halides were synthesized, and their intriguing functional properties were demonstrated. Despite such pioneering works, lead-free double perovskite halides with better crystallinity are still in demand for applications to novel optoelectronic devices. Here, we realized highly crystalline Cs2AgBiBr6 single crystals with a well-defined atomic ordering on the microscopic scale. We avoided the formation of Ag vacancies and the subsequent secondary Cs3Bi2Br9 by manipulating the initial chemical environments in hydrothermal synthesis. The suppression of Ag vacancies allows us to reduce the trap density in the as-grown crystals and to enhance the carrier mobility further. Our design strategy is applicable for fabricating other lead-free halide materials with high crystallinity.
- Subjects :
- Electron mobility
Materials science
Halide
FOS: Physical sciences
Nanotechnology
02 engineering and technology
010402 general chemistry
01 natural sciences
Microscopic scale
Crystallinity
Lead-free
Physics - Chemical Physics
Optoelectronic materials
Cs2AgBiBr6
lcsh:TA401-492
Hydrothermal synthesis
Perovskite (structure)
Chemical Physics (physics.chem-ph)
Condensed Matter - Materials Science
Single crystal
Metals and Alloys
Materials Science (cond-mat.mtrl-sci)
Double perovskite
021001 nanoscience & nanotechnology
0104 chemical sciences
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
lcsh:Materials of engineering and construction. Mechanics of materials
0210 nano-technology
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Journal of Materiomics, Vol 6, Iss 4, Pp 651-660 (2020)
- Accession number :
- edsair.doi.dedup.....39835d83b9374b1e084fceeaf0448609
- Full Text :
- https://doi.org/10.48550/arxiv.2006.15818