J
Jingzhe Zhang
Researcher at China University of Geosciences (Beijing)
Publications - 7
Citations - 24
Jingzhe Zhang is an academic researcher from China University of Geosciences (Beijing). The author has contributed to research in topics: Chemistry & Engineering. The author has an hindex of 1, co-authored 1 publications receiving 4 citations.
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Journal ArticleDOI
Co/Fe3O4 Nanoparticles Embedded in N-doped Hierarchical Porous Carbon Derived from Zeolitic Imidazolate Frameworks as Efficient Oxygen Reduction Electrocatalysts for Zinc-Air Battery-based Desalination
Jinhong Dai,Jingzhe Zhang,R. Karthick,Mengjun Liang,Qiang Wei,Xuncai Chen,Yumeng Shi,Shengli Zhai,Guannan Wang,Fuming Chen +9 more
TL;DR: Zinc-air battery-based desalination (ZABD) is a potential solution to effectively desalinate brackish water and supply energy simultaneously, which requires catalysts with high and durable electrocatalytic activity for oxygen reduction reaction as discussed by the authors .
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Defect Engineering in g-C_3N_4 Quantum-Dot-Modified TiO_2 Nanofiber: Uncovering Novel Mechanisms for the Degradation of Tetracycline in Coexistence with Cu^2+
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An easy-to-synthesize multi-photoresponse smart sensor for rapidly detecting Zn2+ and quantifying Fe3+ based on the enol/keto binding mode
TL;DR: A readily available 4-diethylaminosalicylaldazine-modified fluorene Schiff base (EASA-F) was designed and synthesized through a one-step reaction as mentioned in this paper.
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Plasma boosted the conversion of waste plastics into liquid fuel by a peroxymonosulfate-hydrothermal process
TL;DR: In this paper , a facile plasma treatment method was proposed to modify the plastic surface, aimed to boost the conversion of waste plastics into liquid fuel through a peroxymonosulfate (PMS) coupled hydrothermal process.
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Role of solvent in plasma-assisted peroxymonosulfate-hydrothermal process for plastic conversion.
TL;DR: In this article , the role of solvent in the peroxymonosulfate-hydrothermal process was investigated and the results indicated that increased pressure caused by the solvent greatly reduced the surface reaction and forced the hydrophilic groups to shift back to the carbon chain, thereby reducing the reaction kinetics.