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Jing Shao

Researcher at Shenzhen University

Publications -  5
Citations -  112

Jing Shao is an academic researcher from Shenzhen University. The author has contributed to research in topics: Oxide & Surface modification. The author has an hindex of 4, co-authored 5 publications receiving 37 citations.

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Multiple Effects of Iron and Nickel Additives on the Properties of Proton Conducting Yttrium-Doped Barium Cerate-Zirconate Electrolytes for High-Performance Solid Oxide Fuel Cells.

TL;DR: It is found that transition metal additives also affect the electrical properties, stability, and even catalytic activity of proton-conducting ABO3-type perovskites and for the first time, a positive function of Fe additive is found in BCZY that it not only acts as a good sintering aid but also improves the electrical performance and stability of theBCZY electrolyte in CO2 and H2O at reduced temperatures.
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Surface Defect Engineering on Perovskite Oxides as Efficient Bifunctional Electrocatalysts for Water Splitting.

TL;DR: In this article, a surface defect engineering method is developed for optimizing the electrocatalytic activity of perovskite oxides for water electrolysis, which is found to not only increase the exposure and decrease the coordination of B-site metals but also effectively modulate the electronic structure of these metals.
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Crossing the bridge from molecular catalysis to a heterogenous electrode in electrocatalytic water oxidation.

TL;DR: This work describes an efficient strategy that combines silane surface functionalization and reductive electropolymerization to bind a molecular catalyst on conductive substrates for sustained catalytic water oxidation and addresses issues with limited surface stabilities.
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Stable Molecular Surface Modification of Nanostructured, Mesoporous Metal Oxide Photoanodes by Silane and Click Chemistry.

TL;DR: The chromophore-modified electrodes display enhanced photochemical and electrochemical stabilities compared to phosphonate surface binding with extended photoelectrochemical oxidation of hydroquinone for more than ∼6 h with no significant decay.