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The Influence of Water Vapor on the Electrochemical Shift of an Ionic Liquid Measured by Ambient Pressure X-ray Photoelectron Spectroscopy
Authors:Dr Meng Jia  Dr Alicia Broderick  Dr John T Newberg
Institution:1. Department of Chemistry and Biochemistry, University of Delaware, Newark, DE, 19716 USA;2. Department of Chemistry and Biochemistry, University of Delaware, Newark, DE, 19716 USA

Present Address: U.S. Department of Homeland Security, Science and Technology Directorate's Transportation Security Laboratory, Atlantic City, NJ, 08405 USA;3. Material Science and Technology Division, Los Alamos National Laboratory, Los Alamos, NM, 87545 USA

Abstract:Ionic liquids (ILs) are considered to be one of the steppingstones to fabricate next generation electrochemical devices given their unique physical and chemical properties. The addition of water to ILs significantly impact electrochemical related properties including viscosity, density, conductivity, and electrochemical window. Herein we utilize ambient pressure X-ray photoelectron spectroscopy (APXPS) to examine the impact of water on values of the electrochemical shift (S), which is determined by measuring changes in binding energy shifts as a function of an external bias. APXPS spectra of C 1s, O 1s and N 1s regions are examined for the IL 1-butyl-3-methylimidazolium acetate, C4mim]OAc], at the IL/gas interface as a function of both water vapor pressure and external bias. Results reveal that in the absence of water vapor there is an IL ohmic drop between the working electrode and quasi reference electrode, giving rise to chemical specific S values of less than one. Upon introducing water vapor, S values approach one as a function of increasing water vapor pressure, indicating a decrease in the IL ohmic drop as the IL/water mixture becomes more conductive and the potential drop is driven by the electric double layer at the electrode/IL interface.
Keywords:APXPS  ionic liquid  electrochemical shift  ohmic drop  surface chemistry
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