Pressure Induced Assembly and Coalescence of Lead Chalcogenide Nanocrystals
Author(s) -
Lingyao Meng,
Sakun Duwal,
J. Matthew D. Lane,
Tommy Ao,
Brian Stoltzfus,
Marcus D. Knudson,
Changyong Park,
Paul Chow,
Yuming Xiao,
Hongyou Fan,
Yang Qin
Publication year - 2021
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.0c13350
Subject(s) - nanocrystal , chalcogenide , superlattice , coalescence (physics) , nanotechnology , nanorod , faceting , nanocrystalline material , nanostructure , chemistry , chemical physics , femtosecond , lead sulfide , crystallography , materials science , quantum dot , optoelectronics , optics , laser , physics , astrobiology
We report here pressure induced nanocrystal coalescence of ordered lead chalcogenide nanocrystal arrays into one-dimensional (1D) and 2D nanostructures. In particular, atomic crystal phase transitions and mesoscale coalescence of PbS and PbSe nanocrystals have been observed and monitored in situ respectively by wide- and small-angle synchrotron X-ray scattering techniques. At the atomic scale, both nanocrystals underwent reversible structural transformations from cubic to orthorhombic at significantly higher pressures than those for the corresponding bulk materials. At the mesoscale, PbS nanocrystal arrays displayed a superlattice transformation from face-centered cubic to lamellar structures, while no clear mesoscale lattice transformation was observed for PbSe nanocrystal arrays. Intriguingly, transmission electron microscopy showed that the applied pressure forced both spherical nanocrystals to coalesce into single crystalline 2D nanosheets and 1D nanorods. Our results confirm that pressure can be used as a straightforward approach to manipulate the interparticle spacing and engineer nanostructures with specific morphologies and, therefore, provide insights into the design and functioning of new semiconductor nanocrystal structures under high-pressure conditions.
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