Space- and time-resolved small angle X-ray scattering to probe assembly of silver nanocrystal superlattices
Abstract
Abstract The structure of nanocrystal superlattices has been extensively studied and well documented, however, their assembly process is poorly understood. In this work, we demonstrate an in situ space- and time-resolved small angle X-ray scattering measurement that we use to probe the assembly of silver nanocrystal superlattices driven by electric fields. The electric field creates a nanocrystal flux to the surface, providing a systematic means to vary the nanocrystal concentration near the electrode and thereby to initiate nucleation and growth of superlattices in several minutes. Using this approach, we measure the space- and time-resolved concentration and polydispersity gradients during deposition and show how they affect the superlattice constant and degree of order. We find that the field induces a size-selection effect that can reduce the polydispersity near the substrate by 21% leading to better quality crystals and resulting in field strength-dependent superlattice lattice constants.
- Authors:
- Publication Date:
- Research Org.:
- Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)
- Sponsoring Org.:
- USDOE National Nuclear Security Administration (NNSA)
- OSTI Identifier:
- 1619802
- Alternate Identifier(s):
- OSTI ID: 1512593
- Report Number(s):
- LLNL-JRNL-737659
Journal ID: ISSN 2041-1723; 4211; PII: 6734
- Grant/Contract Number:
- AC52-07NA27344
- Resource Type:
- Published Article
- Journal Name:
- Nature Communications
- Additional Journal Information:
- Journal Name: Nature Communications Journal Volume: 9 Journal Issue: 1; Journal ID: ISSN 2041-1723
- Publisher:
- Nature Publishing Group
- Country of Publication:
- United Kingdom
- Language:
- English
- Subject:
- 36 MATERIALS SCIENCE
Citation Formats
Yu, Yixuan, Yu, Dian, Sadigh, Babak, and Orme, Christine A. Space- and time-resolved small angle X-ray scattering to probe assembly of silver nanocrystal superlattices. United Kingdom: N. p., 2018.
Web. doi:10.1038/s41467-018-06734-9.
Yu, Yixuan, Yu, Dian, Sadigh, Babak, & Orme, Christine A. Space- and time-resolved small angle X-ray scattering to probe assembly of silver nanocrystal superlattices. United Kingdom. https://doi.org/10.1038/s41467-018-06734-9
Yu, Yixuan, Yu, Dian, Sadigh, Babak, and Orme, Christine A. Thu .
"Space- and time-resolved small angle X-ray scattering to probe assembly of silver nanocrystal superlattices". United Kingdom. https://doi.org/10.1038/s41467-018-06734-9.
@article{osti_1619802,
title = {Space- and time-resolved small angle X-ray scattering to probe assembly of silver nanocrystal superlattices},
author = {Yu, Yixuan and Yu, Dian and Sadigh, Babak and Orme, Christine A.},
abstractNote = {Abstract The structure of nanocrystal superlattices has been extensively studied and well documented, however, their assembly process is poorly understood. In this work, we demonstrate an in situ space- and time-resolved small angle X-ray scattering measurement that we use to probe the assembly of silver nanocrystal superlattices driven by electric fields. The electric field creates a nanocrystal flux to the surface, providing a systematic means to vary the nanocrystal concentration near the electrode and thereby to initiate nucleation and growth of superlattices in several minutes. Using this approach, we measure the space- and time-resolved concentration and polydispersity gradients during deposition and show how they affect the superlattice constant and degree of order. We find that the field induces a size-selection effect that can reduce the polydispersity near the substrate by 21% leading to better quality crystals and resulting in field strength-dependent superlattice lattice constants.},
doi = {10.1038/s41467-018-06734-9},
journal = {Nature Communications},
number = 1,
volume = 9,
place = {United Kingdom},
year = {Thu Oct 11 00:00:00 EDT 2018},
month = {Thu Oct 11 00:00:00 EDT 2018}
}
https://doi.org/10.1038/s41467-018-06734-9
Web of Science
Figures / Tables:
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