Jonnathan Medina-Ramos, Ph.D.
Affiliations: | 2013- | Chemistry | University of Delaware, Newark, DE, United States |
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Publications
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Meng K, Medina-Ramos J, Yibeltal-Ashenafi E, et al. (2018) Interplay of proton and electron transfer to determine concerted behavior in the proton-coupled electron transfer of glutathione oxidation. Physical Chemistry Chemical Physics : Pccp |
Li X, Lee SS, Li M, et al. (2018) Effect of nitrogen passivation on interface composition and physical stress in SiO2/SiC(4H) structures Applied Physics Letters. 113: 131601 |
Medina-Ramos J, Zhang W, Yoon K, et al. (2018) Cathodic Corrosion at the Bismuth–Ionic Liquid Electrolyte Interface under Conditions for CO2 Reduction Chemistry of Materials. 30: 2362-2373 |
Medina-Ramos J, Lee SS, Fister TT, et al. (2017) Correction to Structural Dynamics and Evolution of Bismuth Film Electrodes during Electrochemical Reduction of CO2 in Imidazolium-Based Ionic Liquid Solutions Acs Catalysis. 7: 8366-8366 |
Medina-Ramos J, Lee SS, Fister TT, et al. (2017) Structural Dynamics and Evolution of Bismuth Electrodes during Electrochemical Reduction of CO2 in Imidazolium-Based Ionic Liquid Solutions Acs Catalysis. 7: 7285-7295 |
Medina-Ramos J, Pupillo RC, Keane TP, et al. (2015) Efficient Conversion of CO₂ to CO Using Tin and Other Inexpensive and Easily Prepared Post-Transition Metal Catalysts. Journal of the American Chemical Society. 137: 5021-7 |
Medina-Ramos J, DiMeglio JL, Rosenthal J. (2014) Efficient reduction of CO2 to CO with high current density using in situ or ex situ prepared Bi-based materials. Journal of the American Chemical Society. 136: 8361-7 |
Medina-Ramos J, Oyesanya O, Alvarez JC. (2013) Buffer effects in the kinetics of concerted proton-coupled electron transfer: The electrochemical oxidation of glutathione mediated by [IrCl 6]2-at Variable Buffer p K a and concentration Journal of Physical Chemistry C. 117: 902-912 |
Medina-Ramos J, Alligrant TM, Clingenpeel A, et al. (2012) Comparing the hydrogen-bonding effect of brönsted bases in solution and when they are covalently bound to the surface of glassy carbon electrodes in the electrochemical behavior of hydroquinone Journal of Physical Chemistry C. 116: 20447-20457 |