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Relevant bibliographies by topics / Cation hydronium

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Academic literature on the topic 'Cation hydronium'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Cation hydronium"

1

Wallace, Sonjae, Lulu Huang, Chérif F. Matta, Lou Massa, and Ivan Bernal. "New structures of hydronium cation clusters." Comptes Rendus Chimie 15, no. 8 (2012): 700–707. http://dx.doi.org/10.1016/j.crci.2012.04.010.

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Akbari, Saeed, Mohammad Taghi Hamed Mosavian, Fatemeh Moosavi, and Ali Ahmadpour. "Elucidating the morphological aspects and proton dynamics in a hybrid perfluorosulfonic acid membrane for medium-temperature fuel cell applications." Physical Chemistry Chemical Physics 20, no. 47 (2018): 29778–89. http://dx.doi.org/10.1039/c8cp05377d.

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3

Ma, Jun, Shinichi Yamashita, Yusa Muroya, Yosuke Katsumura, and Mehran Mostafavi. "Deciphering the reaction between a hydrated electron and a hydronium ion at elevated temperatures." Physical Chemistry Chemical Physics 17, no. 35 (2015): 22934–39. http://dx.doi.org/10.1039/c5cp04293c.

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4

Yoo, Suhwan, Sejin Park, and Yun Jeong Hwang. "Exploring the Impact of Excess Cations in Acidic CO₂ Reduction Reaction." ECS Meeting Abstracts MA2024-02, no. 61 (2024): 4134. https://doi.org/10.1149/ma2024-02614134mtgabs.

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To anticipate high performance in the electrocatalytic reactions, a comprehensive understanding of the electric double layer (EDL) is essential. Experimental, spectroscopic, and computational studies of the EDL have been reported for understanding the performance in electrocatalytic reactions such as the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and CO2 reduction reaction (CO2RR). Notably, in the CO2RR, previous studies have revealed the accumulation of cations near the outer Helmholtz plane (OHP) significantly has an impact on the reaction performance, product select

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5

Bialonska, Agata, and Ivan Bernal. "A new cyclic hydronium di-cation of composition H18O82+." Comptes Rendus Chimie 10, no. 3 (2007): 232–33. http://dx.doi.org/10.1016/j.crci.2006.10.005.

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6

Escamilla-Roa, Elizabeth, Fernando Nieto, and C. Ignacio Sainz-Díaz. "Stability of the Hydronium Cation in the Structure of Illite." Clays and Clay Minerals 64, no. 4 (2016): 413–24. http://dx.doi.org/10.1346/ccmn.2016.0640406.

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7

Chênevert, Robert, Daniel Chamberland, Michel Simard, and François Brisse. "The crystal and molecular structures of two isostructural complexes: [(H3O•18-crown-6)2(ZnCl4)] and [(H3O•18-crown-6)2(MnCl4)]." Canadian Journal of Chemistry 68, no. 6 (1990): 797–803. http://dx.doi.org/10.1139/v90-127.

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New macrocycle polyether 18-crown-6 complexes of stoichiometry [(H3O+•18-crown-6)2(MC42−)] have been synthesized for M = Zn and Mn. The two complexes are isostructural and crystallize in the monoclinic system, space group C2/c. The unit cell dimensions are as follows: a = 16.229(9), b = 11.535(3), c = 20.134(8) Å, β = 97.55(4)° and a = 16.255(6), b = 11.625(3), c = 20.122(8) Å, β = 96.54(3)° for the Zn and Mn complexes respectively. In both crystal structures (final Rw = 0.048 with 1817 reflections for Zn and Rw = 0.074 with 728 reflections for Mn), the crown ether molecule and the H3O+ cation

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8

Mendes, Ricardo F., Nutalapati Venkatramaiah, João P. C. Tomé, and Filipe A. Almeida Paz. "Crystal structure of a compact three-dimensional metal–organic framework based on Cs+and (4,5-dicyano-1,2-phenylene)bis(phosphonic acid)." Acta Crystallographica Section E Crystallographic Communications 72, no. 12 (2016): 1794–98. http://dx.doi.org/10.1107/s2056989016016765.

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A new metal–organic framework compound, poly[[μ7-dihydrogen (4,5-dicyano-1,2-phenylene)diphosphonato](oxonium)caesium], [Cs(C8H4N2O6P2)(H3O)]n(I), based on Cs+and the organic linker 4,5-dicyano-1,2-phenylene)bis(phosphonic acid, (H4cpp), containing two distinct coordinating functional groups, has been prepared by a simple diffusion method and its crystal structure is reported. The coordination polymeric structure is based on a CsO8N2complex unit comprising a monodentate hydronium cation, seven O-atom donors from two phosphonium groups of the (H2cpp)2−ligand, and two N-atom donors from bridging

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9

Kolesnikov, Alexander V., and Egor I. Ageenko. "Discharge of hydronium ions on metal cathodes in the presence of pyridine." Butlerov Communications 63, no. 8 (2020): 58–63. http://dx.doi.org/10.37952/roi-jbc-01/20-63-8-58.

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In this work, studies have been carried out on the electrochemical reduction of hydrogen (hydronium ion) from acidic aqueous solutions in the presence of an organic substance – pyridine. Electrolysis was carried out in an electrolyte with a sulfuric acid content (0.18; 0.36 M) with a pyridine additions of 8.4·10-3 M. Potentiostatic studies were carried out on a Potentiostat P-30Jcom Elins potentiostat using a three-electrode cell. Working electrodes (cathodes) were made of M1 copper with an area (S) of 0.09 cm2; aluminum (AD1) S – 0.125 cm2, zinc (Ts0A) S – 0.35 cm2, lead (Cl) S – 0.20 cm2, au

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10

Poyraz, Altug S., Jianping Huang, Bingjie Zhang, Amy C. Marschilok, Kenneth J. Takeuchi, and Esther S. Takeuchi. "Synthesis of Cation and Water Free Cryptomelane Type OMS-2 Cathode Materials: The Impact of Tunnel Water on Electrochemistry." MRS Advances 2, no. 7 (2017): 407–12. http://dx.doi.org/10.1557/adv.2017.68.

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ABSTRACTCryptomelane type manganese dioxides (α-MnO2, OMS-2) are interesting potential cathode materials due to the ability of their one dimensional (1D) tunnels to reversibly host various cations including Li+ and an accessible stable 3+/4+ redox couple. Here, we synthesized metal cation free OMS-2 materials where the tunnels were occupied by only water and hydronium ions. Water was subsequently removed from the tunnels. Cation free OMS-2 and Dry-OMS-2 were used as cathodes in Li based batteries to investigate the role of tunnel water on their electrochemistry. The initial discharge capacity

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Books on the topic "Cation hydronium"

1

United States. National Aeronautics and Space Administration., ed. Ca-rich carbonate melts: A regular-solution model, with applications to carbonatite magma + vapor equilibria and carbonate lavas on Venus. National Aeronautics and Space Administration, 1995.

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2

United States. National Aeronautics and Space Administration., ed. Ca-rich carbonate melts: A regular-solution model, with applications to carbonatite magma + vapor equilibria and carbonate lavas on Venus. National Aeronautics and Space Administration, 1995.

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3

United States. National Aeronautics and Space Administration., ed. Ca-rich carbonate melts: A regular-solution model, with applications to carbonatite magma + vapor equilibria and carbonate lavas on Venus. National Aeronautics and Space Administration, 1995.

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Ca-rich carbonate melts: A regular-solution model, with applications to carbonatite magma + vapor equilibria and carbonate lavas on Venus. National Aeronautics and Space Administration, 1995.

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Conference papers on the topic "Cation hydronium"

1

Hossan, Mohammad R., Talukder Z. Jubery, Danny R. Bottenus, Prashanta Dutta, Cornelius F. Ivory, and Wenji Dong. "Preconcentration of Cardiac Proteins in a Cascade Microchip." In ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-63812.

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Concentration of bio-molecules prior to detection is very critical in the development of an integrated, multifunctional lab-on-a chip device for detection of ultra trace molecules from complex biological fluids such as serum, urine, or saliva. In this work, the preconcentration of a clinically relevant biomarker, cardiac troponin I (cTnI), is demonstrated in a cascade microfluidic channel using cationic isotachophoresis (ITP). The cascade chip is formed on PMMA (poly methyl methacrylate) with gradual changes in size both in width and depth direction to achieve a 100× reduction in overall cross

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