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Atanu Rana

Researcher at Indian Association for the Cultivation of Science

Publications -  30
Citations -  1196

Atanu Rana is an academic researcher from Indian Association for the Cultivation of Science. The author has contributed to research in topics: Catalysis & Porphyrin. The author has an hindex of 14, co-authored 28 publications receiving 842 citations. Previous affiliations of Atanu Rana include Ewha Womans University & Indian National Association.

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Molecular electrocatalysts for the oxygen reduction reaction

TL;DR: In this paper, a review of recent developments in homogeneous and heterogeneous molecular ORR catalysis, placing emphasis on reaction mechanisms and the factors governing rates and selectivities, is presented.
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Cobalt Corrole Catalyst for Efficient Hydrogen Evolution Reaction from H2O under Ambient Conditions: Reactivity, Spectroscopy, and Density Functional Theory Calculations

TL;DR: Density functional theory (DFT) calculations indicate that the electron density on a putative hydride species is delocalized off from the H atom into the macrocycle, which makes the protonation of a [Co(III)-H](-) species the rate determining step for the HER consistent with the experimental data.
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The cobalt corrole catalyzed hydrogen evolution reaction: surprising electronic effects and characterization of key reaction intermediates

TL;DR: A surprising effect of halide substituents on reduction potentials and catalytic activity of halogenated cobalt corroles has been deduced by experimental and computational methods as discussed by the authors.
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Intermediates Involved in the 2e–/2H+ Reduction of CO2 to CO by Iron(0) Porphyrin

TL;DR: The reduction of CO2 by an iron porphyrin complex with a hydrogen bonding distal pocket involves at least two intermediates and the facile heterolytic cleavage of the C-OH bond in intermediate II requires strong acids.
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Rational Design of Mononuclear Iron Porphyrins for Facile and Selective 4e–/4H+ O2 Reduction: Activation of O–O Bond by 2nd Sphere Hydrogen Bonding

TL;DR: A series of mononuclear iron porphyrin complexes are rationally designed to achieve efficient O-O bond activation and site-selective proton transfer to effect facile and selective electrochemical reduction of O2 to water with rate constants higher than all known heme/Cu complexes.