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Kirill Kovnir

Researcher at Iowa State University

Publications -  233
Citations -  7160

Kirill Kovnir is an academic researcher from Iowa State University. The author has contributed to research in topics: Crystal structure & Clathrate hydrate. The author has an hindex of 37, co-authored 209 publications receiving 5959 citations. Previous affiliations of Kirill Kovnir include Tokyo Institute of Technology & Max Planck Society.

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One-Step Synthesis of Self-Supported Nickel Phosphide Nanosheet Array Cathodes for Efficient Electrocatalytic Hydrogen Generation.

TL;DR: A convenient and straightforward approach to the synthesis of a three-dimensional (3D) self-supported biphasic Ni5 P4 -Ni2 P nanosheet (NS) array cathode is presented, which is obtained by direct phosphorization of commercially available nickel foam using phosphorus vapor.
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Pd−Ga Intermetallic Compounds as Highly Selective Semihydrogenation Catalysts

TL;DR: The intermetallic compounds Pd(3)Ga(7), PdGa, and Pd (2)Ga are found to be highly selective semihydrogenation catalysts for acetylene outperforming established systems.
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Al13Fe4 as a low-cost alternative for palladium in heterogeneous hydrogenation

TL;DR: This work has identified the low-cost and environmentally benign intermetallic compound Al(13)Fe(4) as an active and selective semi-hydrogenation catalyst, which might prove applicable to a wide range of heterogeneously catalysed reactions.
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Hydrothermal synthesis and characterization of nanorods of various titanates and titanium dioxide

TL;DR: The formation process of titania based nanorod during hydrothermal synthesis starting from an amorphous TiO2.nH2O gel has been investigated and structural defects of the synthesized nanorods were investigated by high-resolution electron microscope.
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Palladium-Gallium Intermetallic Compounds for the Selective Hydrogenation of Acetylene: Part II: Surface Characterization and Catalytic Performance

TL;DR: In this paper, the performance of PdGa and Pd3Ga7 was investigated under different acetylene hydrogenation reaction conditions, in absence and in excess of ethylene, in temperature-programmed and isothermal long-term experiments.