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Institution

Jilin University

EducationChangchun, China
About: Jilin University is a education organization based out in Changchun, China. It is known for research contribution in the topics: Catalysis & Apoptosis. The organization has 101453 authors who have published 88966 publications receiving 1444456 citations. The organization is also known as: Jílín Dàxué.
Topics: Catalysis, Apoptosis, Cancer, Adsorption, Cell growth


Papers
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Journal ArticleDOI
TL;DR: It is demonstrated here that EGFR activation results in disruption of the complex of beta- catenin and alpha-catenin, thereby abrogating the inhibitory effect of alpha-Catenin on beta-catsenin transactivation via CK2alpha-dependent phosphorylation ofalpha-catanin at S641.

245 citations

Journal ArticleDOI
TL;DR: In this paper, X-ray diffraction and atom-force microscopy were applied to characterize the structure and surface morphology of the deposited ZnO films, which were characterized by photoluminescence with an Ar ion laser as a light source.

245 citations

Journal ArticleDOI
TL;DR: Series experiments indicate that PGCS can only be formed when using an iron-based catalyst that can generate a carburized phase during the pyrolytic process, and holds great promise for preparing PGCS from natural resources, including cornstalks, as advanced electrodes in supercapacitors.
Abstract: Porous graphitic carbon nanosheets (PGCS) are synthesized by an in situ self-generating template strategy based on the carburized effect of iron with cornstalks. Cornstalks firstly coordinate with [Fe(CN)(6)](4-) ions to form the cornstalk-[Fe(CN)(6)](4-) precursor. After carbonization and removal of the catalyst, PGCS are obtained. Series experiments indicate that PGCS can only be formed when using an iron-based catalyst that can generate a carburized phase during the pyrolytic process. The unique structures of PGCS exhibit excellent capacitive performance. The PGCS-1-1100 sample (synthesized from 0.1 M [Fe(CN)(6)](4-) with a carbonization temperature of 1100 °C), which shows excellent electrochemical capacitance (up to 213 F g(-1) at 1 A g(-1)), cycling stability, and rate performance in 6 M KOH electrolyte. In the two-electrode symmetric supercapacitors, the maximum energy densities that can be achieved are as high as 9.4 and 61.3 Wh kg(-1) in aqueous and organic electrolytes, respectively. Moreover, high energy densities of 8.3 and 40.6 Wh kg(-1) are achieved at the high power density of 10.5 kW kg(-1) in aqueous and organic electrolytes, respectively. This strategy holds great promise for preparing PGCS from natural resources, including cornstalks, as advanced electrodes in supercapacitors.

245 citations

Journal ArticleDOI
TL;DR: In this paper, the performance of Co-doped ZnO nanofibers is compared with pure ZnOs and showed that Co-depletion can improve the performance at 360°C.
Abstract: Pure and Co-doped (0.3 wt%, 0.5 wt%, and 1 wt%) ZnO nanofibers are synthesized by an electrospinning method and followed by calcination. The as-synthesized nanofibers are characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray (EDX) spectroscopy. Comparing with pure ZnO nanofibers, Co-doped nanofibers exhibit improved acetone sensing properties at 360 °C. The response of 0.5 wt% Co-doped ZnO nanofibers to 100 ppm acetone is about 16, which is 3.5 times larger than that of pure nanofibers (about 4.4). The response and recovery times of 0.5 wt% Co-doped ZnO nanofibers to 100 ppm acetone are about 6 and 4 s, respectively. Moreover, Co-doped ZnO nanofibers can successfully distinguish acetone and ethanol/methanol, even in a complicated ambience. The high response and quick response/recovery are based on the one-dimensional nanostructure of ZnO nanofibers combining with the Co-doping effect. The selectivity is explained by the different optimized operating temperatures of Co-doped ZnO nanofibers to different gases.

244 citations

Journal ArticleDOI
TL;DR: In this paper, the size and morphology controlled NaYF4:Yb, Er nanocrystals were synthesized via the hydrothermal method and the phase transformation from cubic to hexagonal was found to be sensitive to reaction time and reactant concentration.
Abstract: Size and morphology controlled NaYF4:Yb, Er nanocrystals were synthesized via the hydrothermal method. Polydentate ligands, such as EDTA and citrate, were used in the synthesis of cubic and hexagonal Yb3+, Er3+ codoped NaYF4 nanocrystals as a means of controlling the size and morphology of the nanocrystals. Subsequently, the particle size was found to be dependent on the nucleation rate, which, in turn, was governed by the reactant concentration, molar ratio and choice of ligand. The phase transformation from cubic to hexagonal was found to be sensitive to reaction time and reactant concentration. The upconversion photoluminescence of the nanocrystals demonstrated morphology dependence, which provides a means to characterize their crystalline quality and structure.

244 citations


Authors

Showing all 101943 results

NameH-indexPapersCitations
Yang Yang1712644153049
Yury Gogotsi171956144520
Lei Jiang1702244135205
Gang Chen1673372149819
Dongyuan Zhao160872106451
Rui Zhang1512625107917
Xiaodong Wang1351573117552
Avelino Corma134104989095
Jie Liu131153168891
Shuai Liu129109580823
Yang Liu1292506122380
Sheng Dai12298563472
Xin Wang121150364930
Simon A. Wilde11839045547
Shaojun Dong11887357337
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023187
20221,197
20218,629
20208,607
20198,049
20186,868