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Christopher J. Barile

Researcher at University of Nevada, Reno

Publications -  76
Citations -  1934

Christopher J. Barile is an academic researcher from University of Nevada, Reno. The author has contributed to research in topics: Electrolyte & Chemistry. The author has an hindex of 18, co-authored 58 publications receiving 1268 citations. Previous affiliations of Christopher J. Barile include University of Illinois at Urbana–Champaign & Stanford University.

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Dynamic Windows with Neutral Color, High Contrast, and Excellent Durability Using Reversible Metal Electrodeposition

TL;DR: In this article, the authors describe a dynamic window based on reversible electrodeposition of Cu and a second metal on transparent indium tin oxide electrodes modified by Pt nanoparticles. But their work is limited to three-electrode cyclic voltammetry experiments.
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The Interplay of Al and Mg Speciation in Advanced Mg Battery Electrolyte Solutions

TL;DR: Analysis shows that the active Mg complex in conditioned MACC is very likely the [Mg2(μ-Cl)3·6THF](+) complex that is observed in the solid state structure, and conditioning creates free Cl(-) in the electrolyte solution, and is suggested to enhance Mg electrodeposition.
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Electrolytic Conditioning of a Magnesium Aluminum Chloride Complex for Reversible Magnesium Deposition

TL;DR: In this paper, the electrochemistry of Mg deposition and dissolution from the magnesium aluminum chloride complex (MACC) is described and a mechanism describing how the conditioning proces is described.
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Hybrid dynamic windows using reversible metal electrodeposition and ion insertion

TL;DR: In this paper, the authors developed a class of dynamic windows that combines reversible metal electrodeposition with ion insertion chemistry, and demonstrated that these hybrid windows cycle at least 4,000 times without degradation and are compatible with flexible substrates.
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Proton transfer dynamics control the mechanism of O2 reduction by a non-precious metal electrocatalyst

TL;DR: It is demonstrated that undesired side products such as H2O2 and O2(-) arise from a mismatch between proton and electron transfer rates, which aids in the development of a comprehensive framework for understanding the ORR and PCET processes in general.