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Rafael Silva

Researcher at Universidade Estadual de Maringá

Publications -  90
Citations -  11600

Rafael Silva is an academic researcher from Universidade Estadual de Maringá. The author has contributed to research in topics: Catalysis & Electrocatalyst. The author has an hindex of 26, co-authored 76 publications receiving 9885 citations. Previous affiliations of Rafael Silva include Rutgers University & Federal Fluminense University.

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Enhanced catalytic activity in strained chemically exfoliated WS 2 nanosheets for hydrogen evolution

TL;DR: Analyses indicate that the enhanced electrocatalytic activity of WS₂ is associated with the high concentration of the strained metallic 1T (octahedral) phase in the as-exfoliated nanosheets.
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Conducting MoS2 Nanosheets as Catalysts for Hydrogen Evolution Reaction

TL;DR: By partially oxidizingMoS2, it is found that the activity of 2H MoS2 is significantly reduced after oxidation, consistent with edge oxidation, and 1T MoS 2 remains unaffected after oxidization, suggesting that edges of the nanosheets are not the main active sites.
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Cu and Cu-Based Nanoparticles: Synthesis and Applications in Catalysis.

TL;DR: A critical appraisal of different synthetic approaches to Cu and Cu-based nanoparticles and copper nanoparticles immobilized into or supported on various support materials (SiO2, magnetic support materials, etc.), along with their applications in catalysis.
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Enhanced Catalytic Activity in Strained Chemically Exfoliated WS2 Nanosheets for Hydrogen Evolution

TL;DR: In this paper, the authors reported atomically thin nanosheets of chemically exfoliated 2H (trigonal prismatic) XS2 as efficient catalysts for hydrogen evolution with very low overpotentials.
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Cobalt‐Embedded Nitrogen‐Rich Carbon Nanotubes Efficiently Catalyze Hydrogen Evolution Reaction at All pH Values

TL;DR: The synthesis of cobalt-embedded nitrogen-rich carbon nanotubes (NRCNTs) that can efficiently electrocatalyze the hydrogen evolution reaction (HER) with activities close to that of Pt and function well under acidic, neutral or basic media alike, allowing them to be coupled with the best available oxygen-evolving catalysts.