| Literature DB >> 31712613 |
Yao Gao1, Enzheng Shi1, Shibin Deng2, Stephen B Shiring1, Jordan M Snaider2, Chao Liang3, Biao Yuan3, Ruyi Song4, Svenja M Janke5, Alexander Liebman-Peláez6,7, Pilsun Yoo8, Matthias Zeller2, Bryan W Boudouris1,2, Peilin Liao8, Chenhui Zhu6, Volker Blum4,5, Yi Yu3, Brett M Savoie1, Libai Huang2, Letian Dou9.
Abstract
Semiconductor quantum-well structures and superlattices are key building blocks in modern optoelectronics, but it is difficult to simultaneously realize defect-free epitaxial growth while fine tuning the chemical composition, layer thickness and band structure of each layer to achieve the desired performance. Here we demonstrate the modulation of the electronic structure-and consequently the optical properties-of organic semiconducting building blocks that are incorporated between the layers of perovskites through a facile solution processing step. Self-aggregation of the conjugated organic molecules is suppressed by functionalization with sterically demanding groups and single crystalline organic-perovskite hybrid quantum wells (down to one-unit-cell thick) are obtained. The energy and charge transfers between adjacent organic and inorganic layers are shown to be fast and efficient, owing to the atomically flat interface and ultrasmall interlayer distance of the perovskite materials. The resulting two-dimensional hybrid perovskites are very stable due to protection given by the bulky hydrophobic organic groups.Entities:
Year: 2019 PMID: 31712613 DOI: 10.1038/s41557-019-0354-2
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427