Institution
Shanghai University
Education•Shanghai, Shanghai, China•
About: Shanghai University is a education organization based out in Shanghai, Shanghai, China. It is known for research contribution in the topics: Microstructure & Graphene. The organization has 59583 authors who have published 56840 publications receiving 753549 citations. The organization is also known as: Shànghǎi Dàxué.
Topics: Microstructure, Graphene, Nonlinear system, Catalysis, Thin film
Papers published on a yearly basis
Papers
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TL;DR: In this article, the Laplace transformation theory was used to derive the sufficient conditions for synchronization between two identical Chua systems with the same fractional order, and the necessary conditions for achieving synchronization between these two systems were derived via Laplace transform theory.
Abstract: Chaos synchronization of two identical Chua systems with the same fractional order is studied by utilizing the Pecora–Carroll (PC) method, the active–passive decomposition (PAD) method, the one-way coupling method and the bidirectional coupling one. The sufficient conditions for achieving synchronization between these two systems are derived via the Laplace transformation theory. Numerical simulations show the effectiveness of the theoretical analyses.
216 citations
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TL;DR: In this paper, a variety of techniques were applied to discuss systematic effect on the morphology, optical, electronic properties and structure of GQDs/mpg-C 3 N 4 composites.
Abstract: Hydroxyl-graphene quantum dots (GQDs) modified mesoporous graphitic carbon nitride (mpg-C 3 N 4 ) composites were fabricated through electrostatic interactions. A variety of techniques were applied to discuss systematic effect on the morphology, optical, electronic properties and structure of GQDs/mpg-C 3 N 4 composites. Remarkably, the 0.5 wt% GQDs/mpg-C 3 N 4 composites exhibited higher photocatalytic activity than that of the pure mpg-C 3 N 4 by using rhodamine B (RhB) and colorless tetracycline hydrochloride (TC) as pollutants under visible light irradiation. The results indicated that uniform dispersion of GQDs on the surface of mpg-C 3 N 4 and intimate contact between the two materials contributed to the enhanced activity. Radical trapping experiments and electron spin resonance tests both certified that the GQDs/mpg-C 3 N 4 composites can generate more O 2 − species and a small fraction of holes for photocatalytic degradation.
216 citations
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TL;DR: In this paper, an interface-induced co-assembly approach towards hierarchically mesoporous carbon/graphene aerogel composites, possessing interconnected macroporous graphene networks covered by highly ordered mesophorous carbon with a diameter of ≈ 9.6 nm, is reported.
Abstract: Hierarchically porous composites with mesoporous carbon wrapping around the macroporous graphene aerogel can combine the advantages of both components and are expected to show excellent performance in electrochemical energy devices. However, the fabrication of such composites is challenging due to the lack of an effective strategy to control the porosity of the mesostructured carbon layers. Here an interface-induced co-assembly approach towards hierarchically mesoporous carbon/graphene aerogel composites, possessing interconnected macroporous graphene networks covered by highly ordered mesoporous carbon with a diameter of ≈9.6 nm, is reported. And the orientation of the mesopores (vertical or horizontal to the surface of the composites) can be tuned by the ratio of the components. As the electrodes in supercapacitors, the resulting composites demonstrate outstanding electrochemical performances. More importantly, the synthesis strategy provides an ideal platform for hierarchically porous graphene composites with potential for energy storage and conversion applications.
216 citations
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TL;DR: The design of a core-shell structure is effective to promote the performance of deNOx catalysts and can prevent the generation of ammonium sulfate species from blocking the active sites but also inhibit the formation of manganese sulfate, resulting in a higher SO2-tolerance.
Abstract: Developing low-temperature deNOx catalysts with high catalytic activity, SO2-tolerance and stability is highly desirable but remains challenging. Herein, by coating the mesoporous TiO2 layers on carbon nanotubes (CNTs)-supported MnOx and CeOx nanoparticles (NPs), we obtained a core–shell structural deNOx catalyst with high catalytic activity, good SO2-tolerance and enhanced stability. Transmission electron microscopy, X-ray diffraction, N2 sorption, X-ray photoelectron spectroscopy, H2 temperature-programmed reduction and NH3 temperature-programmed desorption have been used to elucidate the structure and surface properties of the obtained catalysts. Both the specific surface area and chemisorbed oxygen species are enhanced by the coating of meso-TiO2 sheaths. The meso-TiO2 sheaths not only enhance the acid strength but also raise acid amounts. Moreover, there is a strong interaction among the manganese oxide, cerium oxide and meso-TiO2 sheaths. Based on these favorable properties, the meso-TiO2 coated catalyst exhibits a higher activity and more extensive operating-temperature window, compared to the uncoated catalyst. In addition, the meso-TiO2 sheaths can serve as an effective barrier to prevent the aggregation of metal oxide NPs during stability testing. As a result, the meso-TiO2 overcoated catalyst exhibits a much better stability than the uncoated one. More importantly, the meso-TiO2 sheaths can not only prevent the generation of ammonium sulfate species from blocking the active sites but also inhibit the formation of manganese sulfate, resulting in a higher SO2-tolerance. These results indicate that the design of a core–shell structure is effective to promote the performance of deNOx catalysts.
216 citations
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TL;DR: The graphene-wrapped CoS nanoparticles are synthesized by a solvothermal approach and exhibits an unprecedented high reversible capacity of 1056 mA h/g among all cobalt sulfide-based anode materials.
Abstract: Graphene-wrapped CoS nanoparticles are synthesized by a solvothermal approach. The product is significantly different from porous CoS microspheres prepared in the absence of graphene under similar preparation conditions. The CoS microspheres and CoS/graphene composite are fabricated as anode materials for lithium-ion batteries. The CoS/graphene composite is found to be better suitable as an anode in terms of higher capacity and better cycling performances. The nanocomposite exhibits an unprecedented high reversible capacity of 1056 mA h/g among all cobalt sulfide-based anode materials. Good cycling performances are also observed at both small and high current rates.
216 citations
Authors
Showing all 59993 results
Name | H-index | Papers | Citations |
---|---|---|---|
Zhong Lin Wang | 245 | 2529 | 259003 |
Yang Yang | 171 | 2644 | 153049 |
Yang Liu | 129 | 2506 | 122380 |
Zhen Li | 127 | 1712 | 71351 |
Xin Wang | 121 | 1503 | 64930 |
Jian Liu | 117 | 2090 | 73156 |
Xin Li | 114 | 2778 | 71389 |
Wei Zhang | 112 | 1189 | 93641 |
Jianjun Liu | 112 | 1040 | 71032 |
Liquan Chen | 111 | 689 | 44229 |
Jin-Quan Yu | 111 | 438 | 43324 |
Jonathan L. Sessler | 111 | 997 | 48758 |
Peng Wang | 108 | 1672 | 54529 |
Qian Wang | 108 | 2148 | 65557 |
Wei Zhang | 104 | 2911 | 64923 |