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Ze-Xing Cai

Researcher at National Institute for Materials Science

Publications -  21
Citations -  1157

Ze-Xing Cai is an academic researcher from National Institute for Materials Science. The author has contributed to research in topics: Catalysis & Electrocatalyst. The author has an hindex of 11, co-authored 19 publications receiving 723 citations. Previous affiliations of Ze-Xing Cai include University of Queensland & Huazhong University of Science and Technology.

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Hollow Functional Materials Derived from Metal-Organic Frameworks: Synthetic Strategies, Conversion Mechanisms, and Electrochemical Applications.

TL;DR: The applications of these hollow structures as electrode materials for lithium-ion batteries, hybrid supercapacitors, and electrocatalysis are presented and an outlook on the emergent challenges and future developments in terms of their controllable fabrications and electrochemical applications is further discussed.
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NO sensing by single crystalline WO3 nanowires

TL;DR: In this article, single crystalline WO 3 nanowires were directly grown on FTO substrates by a hydrothermal approach after calcination at 400°C, and their diameters were mostly in the range of 15-20nm.
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Tailored Catalytic Nanoframes from Metal-Organic Frameworks by Anisotropic Surface Modification and Etching for the Hydrogen Evolution Reaction.

TL;DR: This work proposes a facile anisotropic surface modification and etching strategy for the synthesis of hollow structured ZIF-67 nanoframes that offers insight into the development of metal-organic frameworks with compositional and structural multiplicity, which in turn could encourages more practical catalytic applications.
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Nanoporous ultra-high-entropy alloys containing fourteen elements for water splitting electrocatalysis.

TL;DR: The facile synthesis of nanoporous ultra-high-entropy alloys (np-UHEAs) with hierarchical porosity via dealloying is demonstrated, which exhibit high catalytic activities and electrochemical stabilities in the hydrogen evolution reaction (HER) and oxygen evolution reacted in acidic media, superior to that of commercial Pt/graphene and IrO2 catalysts.