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Wei Xing

Researcher at Chinese Academy of Sciences

Publications -  9
Citations -  1551

Wei Xing is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Catalysis & Platinum. The author has an hindex of 7, co-authored 9 publications receiving 821 citations. Previous affiliations of Wei Xing include University of Science and Technology of China.

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Chemically activating MoS2 via spontaneous atomic palladium interfacial doping towards efficient hydrogen evolution.

TL;DR: P palladium is added into MoS2 materials to activate and stabilize the conductive basal plane to improve the electrocatalytic activity and open the possibility of manipulating the catalytic performance ofMoS2 to rival platinum.
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Climbing the Apex of the ORR Volcano Plot via Binuclear Site Construction: Electronic and Geometric Engineering.

TL;DR: A spontaneously absorbed electron-withdrawing OH ligand was proposed to act proactively as an energy level modifier to empower easy intermediate desorption, while the triangular Fe-Co-OH coordination facilitates O-O bond scission, and this finding opens up a novel strategy to tailor the electronic structure of an atomic site towards boosted activity.
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Engineering Energy Level of Metal Center: Ru Single-Atom Site for Efficient and Durable Oxygen Reduction Catalysis

TL;DR: A novel Ru-SSC with appropriate adsorption free energy of OH* (ΔGOH*) to confer excellent activity and low Fenton reactivity to maintain long-term stability is demonstrated and the practical application of Ru- SSC is validated by showing excellentActivity and stability in a real fuel cell device.
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Enhanced electrocatalytic performance for the hydrogen evolution reaction through surface enrichment of platinum nanoclusters alloying with ruthenium in situ embedded in carbon

TL;DR: In this article, the authors developed a novel matrix architecture in which a trace amount of Pt is alloyed in situ with Ru nanoparticles uniformly and partially embedded in porous carbon spheres, which significantly increase the electrocatalytic activity in the hydrogen evolution process.
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Bridge Bonded Oxygen Ligands between Approximated FeN 4 Sites Confer Catalysts with High ORR Performance

TL;DR: A rational manipulation strategy for introducing axial bonded O to the Fe sites, attained through hexa-coordinating Fe with oxygen functional groups in the precursor, opens up a novel strategy to manage coordination environment at atomic scale towards high activity ORR catalysts.