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Xin Ding

Researcher at Qingdao University

Publications -  81
Citations -  1896

Xin Ding is an academic researcher from Qingdao University. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 17, co-authored 45 publications receiving 1203 citations. Previous affiliations of Xin Ding include Dalian University of Technology & Chinese Academy of Sciences.

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Visible light driven water splitting in a molecular device with unprecedentedly high photocurrent density.

TL;DR: By using the TiO2(1+2) as working electrode in a three-electrode photoelectrochemical cell (PEC), visible light driven water splitting has been successfully demonstrated in a phosphate buffer solution and a high photocurrent density has been achieved.
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A Janus Fe‑SnO 2 Catalyst that Enables Bifunctional Electrochemical Nitrogen Fixation

TL;DR: By means of experiments and density functional theory calculations, it is revealed that the oxygen vacancy-anchored single-atom Fe can effectively adsorb and activate chemical inert N2 molecules, lower the energy barrier for the vital breakage of N≡N, resulting in the enhanced N2 fixation performance.
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Intumescent flame retardant coatings on cotton fabric of chitosan and ammonium polyphosphate via layer-by-layer assembly

TL;DR: In this paper, an intumescent flame retardant coating, composed of cationic chitosan and anion ammonium polyphosphate, has been constructed on cotton fabric by layer-by-layer assembly technique.
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Visible Light-Driven Water Splitting in Photoelectrochemical Cells with Supramolecular Catalysts on Photoanodes

TL;DR: In this paper, a functional water splitting device based on a photoactive anode TiO2(1+2) has been successfully assembled with a molecular photosensitizer 1 and a molecular catalyst 2 connected by coordination of 1 and 2 with Zr4+ ions on the surface of nanostructured TiO 2.
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Artificial photosynthesis – functional devices for light driven water splitting with photoactive anodes based on molecular catalysts

TL;DR: From their performance measurements, it is found that the photoanode TiO2(1 + 3) in which the molecular ruthenium catalyst and the phosphonate anchoring group are linked by a flexible –CH2CH2 CH2– chain showed a significantly higher photocurrent density than thephotoanodeTiO2 (1 + 2) with only –CH 2– linkage.