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Qiang Gao

Researcher at University of Science and Technology of China

Publications -  21
Citations -  3383

Qiang Gao is an academic researcher from University of Science and Technology of China. The author has contributed to research in topics: Catalysis & Cobalt. The author has an hindex of 15, co-authored 21 publications receiving 2651 citations.

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An efficient molybdenum disulfide/cobalt diselenide hybrid catalyst for electrochemical hydrogen generation.

TL;DR: A robust and highly active catalyst for hydrogen evolution reaction that is constructed by in situ growth of molybdenum disulfide on the surface of cobalt diselenide, which is the best among the non-noble metal hydrogen evolution catalysts and even approaches to the commercial platinum/carbon catalyst.
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Nitrogen-doped graphene supported CoSe₂ nanobelt composite catalyst for efficient water oxidation.

TL;DR: The results raise the possibility for the development of effective and robust OER electrodes by using cheap and easily prepared NG-CoSe2 to replace the expensive commercial catalysts such as RuO2 and IrO2.
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"Superaerophobic" Nickel Phosphide Nanoarray Catalyst for Efficient Hydrogen Evolution at Ultrahigh Current Densities.

TL;DR: A Ni2P nanoarray catalyst grown on a commercial Ni foam substrate demonstrates an outstanding electrocatalytic activity and stability in basic electrolyte, and highlights that an aerophobic structure is essential to catalyze gas evolution for large-scale practical applications.
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Doping-induced structural phase transition in cobalt diselenide enables enhanced hydrogen evolution catalysis.

TL;DR: A doping strategy to induce a phase transition in cobalt selenide and boost H2-evolution performance is presented, with striking catalysis performance can be attributed to the favorable electronic structure and local coordination environment created by this doping-induced structural phase transition strategy.
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An Efficient CeO2/CoSe2 Nanobelt Composite for Electrochemical Water Oxidation

TL;DR: The constructed hybrid catalyst shows extremely high oxgen evolution reaction (OER) activity, even beyond the state-of-the-art RuO2 catalyst in alkaline media.