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Title: Salt Effects on Li-Ion Exchange Kinetics of Na2Mg2P3O9N: Systematic In Situ Synchrotron Diffraction Studies

Abstract

The kinetics and thermodynamics of solid-state ion exchange of Li+ into Na2Mg2P3O9N were explored using in situ synchrotron X-ray diffraction methods for a series of Li-containing salts, allowing systematic trends with general applicability to ion exchange reactions to be elucidated. The collection of data for a wide range of reaction conditions was enabled through the use of a novel multi-well sample environment which leverages the ability of the synchrotron beamline to rapidly (~1 second) collect high-quality data suitable for monitoring reaction progress. From this data, it was possible to resolve the influence of salt choice and salt concentration on the ion exchange reaction kinetics. Moreover, by carrying out experiments at different temperatures, initial estimates of activation energies were obtained. It was generally found that the ion exchange reaction kinetics strongly depended on the salt chosen as the ion source rather than being primarily determined by the ion mobility of the ceramic.

Authors:
ORCiD logo [1];  [1];  [1];  [2];  [3]; ORCiD logo [1]; ORCiD logo [2]
  1. Stony Brook Univ., NY (United States)
  2. Stony Brook Univ., NY (United States); Brookhaven National Lab. (BNL), Upton, NY (United States)
  3. Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
Publication Date:
Research Org.:
Energy Frontier Research Centers (EFRC) (United States). A Next Generation Synthesis Center (GENESIS); Stony Brook Univ., NY (United States); Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
OSTI Identifier:
1602770
Grant/Contract Number:  
SC0019212; AC02-06CH11357
Resource Type:
Accepted Manuscript
Journal Name:
Journal of Physical Chemistry. C
Additional Journal Information:
Journal Volume: 124; Journal Issue: 12; Journal ID: ISSN 1932-7447
Publisher:
American Chemical Society
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY

Citation Formats

Cosby, Monty R., Mattei, Gerard S., Wang, Yusu, Li, Zhuo, Bechtold, Nicholas, Chapman, Karena W., and Khalifah, Peter G. Salt Effects on Li-Ion Exchange Kinetics of Na2Mg2P3O9N: Systematic In Situ Synchrotron Diffraction Studies. United States: N. p., 2020. Web. doi:10.1021/acs.jpcc.0c00067.
Cosby, Monty R., Mattei, Gerard S., Wang, Yusu, Li, Zhuo, Bechtold, Nicholas, Chapman, Karena W., & Khalifah, Peter G. Salt Effects on Li-Ion Exchange Kinetics of Na2Mg2P3O9N: Systematic In Situ Synchrotron Diffraction Studies. United States. https://doi.org/10.1021/acs.jpcc.0c00067
Cosby, Monty R., Mattei, Gerard S., Wang, Yusu, Li, Zhuo, Bechtold, Nicholas, Chapman, Karena W., and Khalifah, Peter G. Mon . "Salt Effects on Li-Ion Exchange Kinetics of Na2Mg2P3O9N: Systematic In Situ Synchrotron Diffraction Studies". United States. https://doi.org/10.1021/acs.jpcc.0c00067. https://www.osti.gov/servlets/purl/1602770.
@article{osti_1602770,
title = {Salt Effects on Li-Ion Exchange Kinetics of Na2Mg2P3O9N: Systematic In Situ Synchrotron Diffraction Studies},
author = {Cosby, Monty R. and Mattei, Gerard S. and Wang, Yusu and Li, Zhuo and Bechtold, Nicholas and Chapman, Karena W. and Khalifah, Peter G.},
abstractNote = {The kinetics and thermodynamics of solid-state ion exchange of Li+ into Na2Mg2P3O9N were explored using in situ synchrotron X-ray diffraction methods for a series of Li-containing salts, allowing systematic trends with general applicability to ion exchange reactions to be elucidated. The collection of data for a wide range of reaction conditions was enabled through the use of a novel multi-well sample environment which leverages the ability of the synchrotron beamline to rapidly (~1 second) collect high-quality data suitable for monitoring reaction progress. From this data, it was possible to resolve the influence of salt choice and salt concentration on the ion exchange reaction kinetics. Moreover, by carrying out experiments at different temperatures, initial estimates of activation energies were obtained. It was generally found that the ion exchange reaction kinetics strongly depended on the salt chosen as the ion source rather than being primarily determined by the ion mobility of the ceramic.},
doi = {10.1021/acs.jpcc.0c00067},
journal = {Journal of Physical Chemistry. C},
number = 12,
volume = 124,
place = {United States},
year = {Mon Feb 24 00:00:00 EST 2020},
month = {Mon Feb 24 00:00:00 EST 2020}
}

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