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Hong Liu

Researcher at Shandong University

Publications -  2349
Citations -  79103

Hong Liu is an academic researcher from Shandong University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 100, co-authored 1905 publications receiving 57561 citations. Previous affiliations of Hong Liu include Shanghai University & Guangzhou University.

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High efficiency perovskite solar cells with tailorable surface wettability by surfactant

TL;DR: In this paper, an ultrathin sodium dodecyl benzene sulfonate (SDBS) film is introduced between the perovskite absorber and the NiOx hole transport layer to reduce interfacial and extraction losses.
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Indole derivatives as potent inhibitors of 5-lipoxygenase: design, synthesis, biological evaluation, and molecular modeling.

TL;DR: A series of novel indole derivatives was designed, synthesized and evaluated by cell-based assays for their inhibitory activities against 5-LOX in rat peritoneal leukocytes, showing excellent in vitro activities and may possess potential for the treatment of LT-related diseases.
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Nitrogen-doped carbon encapsulated hollow ZnSe/CoSe2 nanospheres as high performance anodes for lithium-ion batteries.

TL;DR: As an advanced anode, ZnSe/CoSe2@N-C composite shows remarkable cycling stability and exceptional rate capability in the field of energy storage technologies.
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In situ alternative switching between Ti4+ and Ti3+ driven by H2O2 in TiO2 nanostructures: mechanism of pseudo-Fenton reaction

TL;DR: In this article, it was shown that Ti4+ in TiO2 nanostructures can be reduced in situ to Ti3+ in the presence of H2O2 to generate hydroxyl radicals for the oxidation of organic pollutants.
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One novel quinoxaline derivative as a potent human cyclophilin A inhibitor shows highly inhibitory activity against mouse spleen cell proliferation.

TL;DR: A novel quinoxaline derivative, 2,3-di(furan-2-yl)-6-(3-N,N-diethylcarbamoyl-piperidino)carbonylamino quin oxaline (DC838, 3), which was confirmed to be a potent inhibitor against human CypA, and elucidated the specific DC838 binding to CypA at the atomic level.