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Emma L. DeWalt-Kerian

Researcher at University of Alberta

Publications -  6
Citations -  227

Emma L. DeWalt-Kerian is an academic researcher from University of Alberta. The author has contributed to research in topics: Aqueous solution & Chemistry. The author has an hindex of 3, co-authored 4 publications receiving 148 citations.

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Separating the pH-Dependent Behavior of Water in the Stern and Diffuse Layers with Varying Salt Concentration

TL;DR: In this paper, the authors used vibrational sum frequency generation (SFG) spectroscopy to distinguish different populations of water molecules within the electric double layer (EDL) at the silica/water interface.
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pH-Dependent Inversion of Hofmeister Trends in the Water Structure of the Electrical Double Layer

TL;DR: SFG results indicate a direct Hofmeister series of cation adsorption at pH 8 (Li+ < Na+ < K+ < Cs+), with an inversion in SFG intensity trends also occurred at pH < 6, which was attributed to contributions from asymmetric cation hydration and EDL overcharging.
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New Insights into χ(3) Measurements: Comparing Nonresonant Second Harmonic Generation and Resonant Sum Frequency Generation at the Silica/Aqueous Electrolyte Interface

TL;DR: In this paper, different pH-dependent behaviors at the mineral oxide/aqueous electrolyte interface have been observed by nonresonant second harmonic generation (SHG) and resonant sum frequency generators.
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Water Structure in the Electrical Double Layer and the Contributions to the Total Interfacial Potential at Different Surface Charge Densities.

TL;DR: In this article , the individual Stern layer and diffuse layer OH stretching spectra at the silica/water interface in the presence of NaCl over a wide pH range using a combination of vibrational sum frequency generation spectroscopy, heterodyned second harmonic generation, and streaming potential measurements.
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Correction to “pH-Dependent Inversion of Hofmeister Trends in the Water Structure of the Electrical Double Layer”

TL;DR: The pH 11 spectrum for LiCl was missing, and the pH 10−6 spectra were shown to be 1 pH unit lower than the actual pH based on the color sequence shown in the Figure 1 legend, which has been revised.