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Dong Wang

Researcher at Chinese Academy of Sciences

Publications -  586
Citations -  13460

Dong Wang is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Computer science & Medicine. The author has an hindex of 49, co-authored 491 publications receiving 9970 citations. Previous affiliations of Dong Wang include University of Science and Technology of China & Shanghai University.

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Potential Dependent Adsorption Geometry of 2,5-Dihydroxybenzoic Acid on a Au(111) Surface: An in Situ Electrochemical Scanning Tunneling Microscopy Study

TL;DR: In this article, the adsorption and electrochemical behaviors of 2,5-dihydroxybenzoic acid (DHB) at the electrochemical interface of Au(111) electrode and 0.1 M aqueous perchloric acid solution have been studied by cyclic voltammetry and in situ electrochemical scanning tunneling microscopy.
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Integrated Ideal‐Bandgap Perovskite/Bulk‐Heterojunction Solar Cells with Efficiencies > 24%

TL;DR: In this article , the authors reported a highly efficient integrated ideal bandgap perovskite/bulk-heterojunction solar cell (IPBSC) with an inverted architecture, featuring a near infrared (NIR) polymer DTBTI-based bulk heterojunction (BHJ) layer atop guanidinium bromide (GABr) modified FA0.7MA 0.3Pb0.3I3
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Unveiling the Re segregation at γ/γ′ interface in Ni-based superalloy

TL;DR: In this paper, the distribution of Re in a Ni-based single crystal superalloy is specified by atom probe tomography after different heat treatment, and the results provide a novel perspective on the comprehension of the Re effect on γ΄ growth and are valuable to both improving the γ/γ′ microstructure stability and designing high performance superalloys.
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Highly diastereoselective synthesis of N-protected arylglycine derivatives via TiCl4-Promoted Friedel-Crafts reaction of phenols with chiral N, O-hemiacetal

Cheng-Sheng Ge, +2 more
- 01 Dec 2002 - 
TL;DR: The optically active N-protected arylglycine derivatives were obtained via TiCl 4 -promoted Friedel-Crafts reaction of various phenols with chiral N,O-hemiacetals in excellent diastereoselectivity as mentioned in this paper.