Stability limits and defect dynamics in Ag nanoparticles probed by Bragg coherent diffractive imaging
Abstract
Dissolution is critical to nanomaterial stability, especially for partially dealloyed nanoparticle catalysts. Unfortunately, highly active catalysts are often not stable in their reactive environments, preventing widespread application. Thus, focusing on the structure–stability relationship at the nanoscale is crucial and will likely play an important role in meeting grand challenges. Recent advances in imaging capability have come from electron, X-ray, and other techniques but tend to be limited to specific sample environments and/or two-dimensional images. Here, we report investigations into the defect-stability relationship of silver nanoparticles to voltage-induced electrochemical dissolution imaged in situ in three dimensional detail by Bragg coherent diffractive imaging. We first determine the average dissolution kinetics by stationary probe rotating disk electrode in combination with inductively coupled plasma mass spectrometry, which allows in situ measurement of Ag+ ion formation. We then observe the dissolution and redeposition processes in single nanocrystals, providing unique insight about the role of surface strain, defects, and their coupling to the dissolution chemistry. Finally, the methods developed and the knowledge gained go well beyond a “simple” silver electrochemistry and are applicable to all electrocatalytic reactions where functional links between activity and stability are controlled by structure and defect dynamics.
- Publication Date:
- Research Org.:
- Argonne National Laboratory (ANL), Argonne, IL (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES). Materials Sciences and Engineering Division; USDOE Office of Science (SC), Basic Energy Sciences (BES). Scientific User Facilities Division
- OSTI Identifier:
- 1346723
- Grant/Contract Number:
- AC02-06CH11357
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Nano Letters
- Additional Journal Information:
- Journal Volume: 17; Journal Issue: 3; Journal ID: ISSN 1530-6984
- Publisher:
- American Chemical Society
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 36 MATERIALS SCIENCE; 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
Citation Formats
Liu, Y., Lopes, P. P., Cha, W., Harder, R., Maser, J., Maxey, E., Highland, M. J., Markovic, N. M., Hruszkewycz, S. O., Stephenson, G. B., You, H., and Ulvestad, A. Stability limits and defect dynamics in Ag nanoparticles probed by Bragg coherent diffractive imaging. United States: N. p., 2017.
Web. doi:10.1021/acs.nanolett.6b04760.
Liu, Y., Lopes, P. P., Cha, W., Harder, R., Maser, J., Maxey, E., Highland, M. J., Markovic, N. M., Hruszkewycz, S. O., Stephenson, G. B., You, H., & Ulvestad, A. Stability limits and defect dynamics in Ag nanoparticles probed by Bragg coherent diffractive imaging. United States. https://doi.org/10.1021/acs.nanolett.6b04760
Liu, Y., Lopes, P. P., Cha, W., Harder, R., Maser, J., Maxey, E., Highland, M. J., Markovic, N. M., Hruszkewycz, S. O., Stephenson, G. B., You, H., and Ulvestad, A. Fri .
"Stability limits and defect dynamics in Ag nanoparticles probed by Bragg coherent diffractive imaging". United States. https://doi.org/10.1021/acs.nanolett.6b04760. https://www.osti.gov/servlets/purl/1346723.
@article{osti_1346723,
title = {Stability limits and defect dynamics in Ag nanoparticles probed by Bragg coherent diffractive imaging},
author = {Liu, Y. and Lopes, P. P. and Cha, W. and Harder, R. and Maser, J. and Maxey, E. and Highland, M. J. and Markovic, N. M. and Hruszkewycz, S. O. and Stephenson, G. B. and You, H. and Ulvestad, A.},
abstractNote = {Dissolution is critical to nanomaterial stability, especially for partially dealloyed nanoparticle catalysts. Unfortunately, highly active catalysts are often not stable in their reactive environments, preventing widespread application. Thus, focusing on the structure–stability relationship at the nanoscale is crucial and will likely play an important role in meeting grand challenges. Recent advances in imaging capability have come from electron, X-ray, and other techniques but tend to be limited to specific sample environments and/or two-dimensional images. Here, we report investigations into the defect-stability relationship of silver nanoparticles to voltage-induced electrochemical dissolution imaged in situ in three dimensional detail by Bragg coherent diffractive imaging. We first determine the average dissolution kinetics by stationary probe rotating disk electrode in combination with inductively coupled plasma mass spectrometry, which allows in situ measurement of Ag+ ion formation. We then observe the dissolution and redeposition processes in single nanocrystals, providing unique insight about the role of surface strain, defects, and their coupling to the dissolution chemistry. Finally, the methods developed and the knowledge gained go well beyond a “simple” silver electrochemistry and are applicable to all electrocatalytic reactions where functional links between activity and stability are controlled by structure and defect dynamics.},
doi = {10.1021/acs.nanolett.6b04760},
journal = {Nano Letters},
number = 3,
volume = 17,
place = {United States},
year = {Fri Feb 10 00:00:00 EST 2017},
month = {Fri Feb 10 00:00:00 EST 2017}
}
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