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[×ÊÔ´] ×îÐÂnatureÎÄÕ Á¿×ӵ㸴ºÏ¸ÆîÑ¿ó²ÄÁÏQuantum-dot-in-perovskite solids

ÌâÄ¿£ºQuantum-dot-in-perovskite solids
×÷ÕߣºZhijun Ning1*, Xiwen Gong1*, Riccardo Comin1*, GrantWalters1, Fengjia Fan1, Oleksandr Voznyy1, Emre Yassitepe1,
Andrei Buin1, Sjoerd Hoogland1 & Edward H. Sargent1
ÕªÒª£ºHeteroepitaxy¡ªatomically aligned growth of a crystalline filmatop a different crystalline substrate¡ªis the basis of electrically driven
lasers, multijunction solar cells, and blue-light-emitting diodes1¨C5. Crystalline coherence is preserved even when atomic identity is
modulated, a fact that is the critical enabler of quantum wells, wires, and dots6¨C10. The interfacial quality achieved as a result of heteroepitaxial
growth allows new combinations of materials with complementary properties, which enables the design and realization of functionalities that are not available in the single-phase constituents. Herewe showthat organohalide perovskites and preformed colloidal quantum dots, combined in the solution phase, produce epitaxially
aligned ¡®dots-in-a-matrix¡¯ crystals. Using transmission electron microscopy and electron diffraction,we reveal heterocrystals as large as about 60 nanometres and containing at least 20 mutually aligned dots that inherit the crystalline orientation of the perovskite matrix. The heterocrystals exhibit remarkable optoelectronic properties
that are traceable to their atom-scale crystalline coherence: photoelectrons and holes generated in the larger-bandgap perovskites are transferred with 80% efficiency to become excitons in the quantum dot nanocrystals, which exploit the excellent photocarrier diffusion of perovskites to produce bright-light emission
from infrared-bandgap quantum-tuned materials. By combining the electrical transport properties of the perovskite matrix with the
high radiative efficiency of the quantum dots, we engineer a new platform to advance solution-processed infrared optoelectronics.
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