TY - JOUR
T1 - In situ coherent x-ray scattering reveals polycrystalline structure and discrete annealing events in strongly coupled nanocrystal superlattices
AU - Hurley, Matthew J.
AU - Tanner, Christian P.N.
AU - Portner, Joshua
AU - Utterback, James K.
AU - Coropceanu, Igor
AU - Das, Avishek
AU - Slivka, Joseph D.
AU - Fluerasu, Andrei
AU - Sun, Yanwen
AU - Song, Sanghoon
AU - Hamerlynck, Leo M.
AU - Miller, Alexander H.
AU - Bhattacharyya, Priyadarshini
AU - Talapin, Dmitri V.
AU - Williams, Garth J.
AU - Ginsberg, Naomi S.
AU - Teitelbaum, Samuel W.
N1 - Publisher Copyright: © 2024 authors. Published by the American Physical Society. Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI.
PY - 2024/4
Y1 - 2024/4
N2 - Solution-phase bottom up self-assembly of nanocrystals into superstructures such as ordered superlattices is an attractive strategy to generate functional materials of increasing complexity, including very recent advances that incorporate strong interparticle electronic coupling. While the self-assembly kinetics in these systems have been elucidated and related to the product characteristics, the weak interparticle bonding interactions suggest the superstructures formed could continue to order within the solution long after the primary nucleation and growth have occurred, even though the mechanism of annealing remains to be elucidated. Here, we use a combination of Bragg coherent diffractive imaging and x-ray photon correlation spectroscopy to create real-space maps of supercrystalline order along with a real-time view of the strain fluctuations in aging strongly coupled nanocrystal superlattices while they remain suspended and immobilized in solution. By combining the results, we deduce that the self-assembled superstructures are polycrystalline, initially comprising multiple nucleation sites, and that shear avalanches at grain boundaries continue to increase crystallinity long after growth has substantially slowed. This multimodal approach should be generalizable to characterize a breadth of materials in situ in their native chemical environments, thus extending the reach of high-resolution coherent x-ray characterization to the benefit of a much wider range of physical systems.
AB - Solution-phase bottom up self-assembly of nanocrystals into superstructures such as ordered superlattices is an attractive strategy to generate functional materials of increasing complexity, including very recent advances that incorporate strong interparticle electronic coupling. While the self-assembly kinetics in these systems have been elucidated and related to the product characteristics, the weak interparticle bonding interactions suggest the superstructures formed could continue to order within the solution long after the primary nucleation and growth have occurred, even though the mechanism of annealing remains to be elucidated. Here, we use a combination of Bragg coherent diffractive imaging and x-ray photon correlation spectroscopy to create real-space maps of supercrystalline order along with a real-time view of the strain fluctuations in aging strongly coupled nanocrystal superlattices while they remain suspended and immobilized in solution. By combining the results, we deduce that the self-assembled superstructures are polycrystalline, initially comprising multiple nucleation sites, and that shear avalanches at grain boundaries continue to increase crystallinity long after growth has substantially slowed. This multimodal approach should be generalizable to characterize a breadth of materials in situ in their native chemical environments, thus extending the reach of high-resolution coherent x-ray characterization to the benefit of a much wider range of physical systems.
UR - https://www.scopus.com/pages/publications/85192318038
UR - https://www.scopus.com/pages/publications/85192318038#tab=citedBy
U2 - 10.1103/PhysRevResearch.6.023119
DO - 10.1103/PhysRevResearch.6.023119
M3 - Article
SN - 2643-1564
VL - 6
JO - Physical Review Research
JF - Physical Review Research
IS - 2
M1 - 023119
ER -