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Title: In Situ Electrochemical Dilatometry of Phosphate Anion Electrosorption

Journal Article · · Environmental Science & Technology Letters (Online)

Here in this paper we investigate the competitive electrosorption of mono- and divalent phosphate anions through electrochemical desalination- and dilatometry-based experiments. Through in situ dilatometry, we monitor the strain at the electrode surface as anions and cations are electrosorbed. Strain measurements show that the presence of divalent ions promotes a greater than anticipated electrode expansion during cation (Na+) electrosorption. The expansion observed with Na+ equaled the expansion observed with HPO42–. Because the ionic radius of Na+ is smaller than that of HPO42–, the symmetric expansion suggests that divalent anions do not completely desorb during electrode regeneration, causing the adverse interactions with the cation during co-ion expulsion. This results in a decrease in desalination performance, indicated by a decreased salt adsorption capacity. Conversely, an expected asymmetric expansion during anion and cation electrosorption occurs with monovalent phosphate anions (H2PO4–), indicating that monovalent ions can be effectively replaced by the cation at the electrode surface.

Research Organization:
Energy Frontier Research Centers (EFRC) (United States). Fluid Interface Reactions, Structures and Transport Center (FIRST); Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
AC05-00OR22725
OSTI ID:
1491313
Journal Information:
Environmental Science & Technology Letters (Online), Vol. 5, Issue 12; ISSN 2328-8930
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 14 works
Citation information provided by
Web of Science

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Constant chemical potential cycles for capacitive deionization journal January 2019
Composite Electrode Ink Formulation for All Solid-State Batteries journal January 2019

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