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Kulbir Kaur Ghuman

Researcher at University of Toronto

Publications -  31
Citations -  1296

Kulbir Kaur Ghuman is an academic researcher from University of Toronto. The author has contributed to research in topics: Catalysis & Frustrated Lewis pair. The author has an hindex of 14, co-authored 27 publications receiving 874 citations. Previous affiliations of Kulbir Kaur Ghuman include Kyushu University & Institut national de la recherche scientifique.

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Photoexcited Surface Frustrated Lewis Pairs for Heterogeneous Photocatalytic CO2 Reduction

TL;DR: It was found that the surface frustrated Lewis pairs created by a Lewis acidic coordinately unsaturated surface indium site proximal to an oxygen vacancy and a Lewis basic surface hydroxide site in In2O3-x(OH)y become more acidic and basic and hence more active in the ES compared to the GS.
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Illuminating CO2 reduction on frustrated Lewis pair surfaces: investigating the role of surface hydroxides and oxygen vacancies on nanocrystalline In2O3−x(OH)y

TL;DR: Photochemical CO2 reduction is demonstrated at a rate of 150 μmol gcat(-1) hour(-1), which is four times better than the reduction rate in the dark, and a reaction mechanism is proposed whereby a surface active site of In2O(3-x)(OH)y, composed of a Lewis base hydroxide adjacent to a Lewis acid indium, together with an oxygen vacancy, assists the adsorption and heterolytic dissociation of H2 that enables the
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Adsorption and Dissociation of H2O on Monolayered MoS2 Edges: Energetics and Mechanism from ab Initio Simulations

TL;DR: In this article, the authors studied the dissociation of water on 2D monolayer molybdenum disulfide (MoS2) edges with density functional theory.
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Heterogeneous reduction of carbon dioxide by hydride-terminated silicon nanocrystals.

TL;DR: The observation is reported that hydride-terminated silicon nanocrystals with average diameter 3.5 nm, denoted ncSi:H, can function as a single component heterogeneous reducing agent for converting gaseous carbon dioxide selectively to carbon monoxide, at a rate of hundreds of μmol h−1 g−1.