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Institution

University of Science and Technology Beijing

EducationBeijing, China
About: University of Science and Technology Beijing is a education organization based out in Beijing, China. It is known for research contribution in the topics: Microstructure & Alloy. The organization has 41558 authors who have published 44473 publications receiving 623229 citations. The organization is also known as: Beijing Steel and Iron Institute.


Papers
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Journal ArticleDOI
TL;DR: A graphdiyne nanosheet/Pt nanoparticle composite showed outstanding catalytic activity for the reaction of I3−/I− redox pairs, i.e., the best among rGO/Pit nanoparticle composites, Pt nanoparticles and Pt foils as mentioned in this paper.
Abstract: A graphdiyne nanosheet/Pt nanoparticle composite shows outstanding catalytic activity for the reaction of I3−/I− redox pairs, i.e., the best among rGO/Pt nanoparticle composites, Pt nanoparticles and Pt foils. This is ascribed to enhanced electron transfer resulting from the easier chemical interaction between Pt and the triple bond of graphdiyne.

159 citations

Journal ArticleDOI
TL;DR: In this paper, the impact of chlorination and fluorination on the properties of organic solar cells (OSCs) was studied and it was shown that chlorination is more effective than fluorination in downshifting the molecular energy levels and broadening the absorption spectra.
Abstract: Halogenation is a very efficient chemical modification method to tune the molecular energy levels, absorption spectra and molecular packing of organic semiconductors. Recently, in the field of organic solar cells (OSCs), both fluorine- and chlorine-substituted photovoltaic materials, including donors and acceptors, demonstrated their great potentials in achieving high power conversion efficiencies (PCEs), raising a question that how to make a decision between fluorination and chlorination when designing materials. Herein, we systemically studied the impact of fluorination and chlorination on the properties of resulting donors (PBDB-T-2F and PBDB-T-2Cl) and acceptors (IT-4F and IT-4Cl). The results suggest that all the OSCs based on different donor and acceptor combinations can deliver good PCEs around 13%–14%. Chlorination is more effective than fluorination in downshifting the molecular energy levels and broadening the absorption spectra. The influence of chlorination and fluorination on the crystallinity of the resulting materials is dependent on their introduction positions. As chlorination has the advantage of easy synthesis, it is more attractive in designing low-cost photovoltaic materials and therefore may have more potential in large-scale applications.

159 citations

Journal ArticleDOI
TL;DR: In this paper, a template-engaged strategy is adopted to fabricate hollow microspheres derived from a Co-MOF, which can effectively offer space for fast mass transport and electron transfer.
Abstract: Electrocatalytic water splitting has been recognized to be one of the most promising routes to acquire hydrogen. However, the high-efficiency water splitting is limited by the sluggish kinetics of the anodic oxygen evolution reaction (OER). Metal–organic frameworks (MOFs) have been extensively utilized as precursors to synthesize high-performance electrocatalysts. Herein, a facile template-engaged strategy is adopted to fabricate hollow microspheres derived from a Co-MOF. After a thermally induced selenylation process under an argon atmosphere, the Co-MOF is successfully converted into CoSe2 microspheres at different temperatures. The optimized CoSe2-450 microspheres display excellent OER electrocatalytic performance in 1.0 M KOH aqueous solution, exhibiting 10 mA cm−2 at η = 330 mV with a small Tafel slope of 79 mV dec−1, even superior to those of a commercial IrO2 catalyst. Moreover, CoSe2-450 shows excellent durability without obvious decay after 1000 cyclic voltammetry cycles. This is due to the hollow interior of CoSe2 microspheres and well-distributed active sites, which can effectively offer space for fast mass transport and electron transfer.

158 citations

Journal ArticleDOI
TL;DR: In this paper, a facile and environmentally friendly 3D printing approach was proposed to fabricate superhydrophobic membranes with an ordered porous structure for oil-water separation using hydrophobic nanosilica-filled polydimethylsiloxane (PDMS) ink.
Abstract: Although superhydrophobic porous membranes are considered to be very promising candidates for oil–water separation, their fabrication methods often involve complicated treatments to build a coating with micro/nano-features on a porous mesh (called “coating on a mesh structure”), which can lead to weak mechanical stability of the superhydrophobic surfaces and the formation of inhomogeneous membrane pores. Herein, we report a facile and environmentally friendly 3D printing approach to fabricate superhydrophobic membranes with an ordered porous structure for oil–water separation using hydrophobic nanosilica-filled polydimethylsiloxane (PDMS) ink. The addition of nanosilica can improve the mechanical strength of the ink and thus ensures the formation of desired topographical structures without the risk of collapsing during 3D printing. Through adjusting the geometrical parameters, a superhydrophobic PDMS membrane was obtained, which mainly depended on the roughness at the sub-millimeter scale. More importantly, the 3D printing approach described herein integrated the superhydrophobic surface into the porous framework and resulted in a mechanically durable superhydrophobic membrane, which successfully avoids the weak interface adhesion issue that arises from the traditional “coating on a mesh structure.” Moreover, the pore size of the printed membrane could be easily adjusted via a computer program to optimize both the liquid flux and separation efficiency of the membranes. The maximum oil–water separation efficiency (∼99.6%) could be achieved for the printed porous membrane with the pore size of 0.37 mm, which also exhibited a high flux of ∼23 700 L m−2 h−1.

158 citations

Journal ArticleDOI
TL;DR: The simulation results show that the framework of the fog computing after Cloud Atomization can build the system network flexibly, and dynamic load balancing mechanism can effectively configure system resources as well as reducing the consumption of node migration brought by system changes.
Abstract: Because of cloud computing's high degree of polymerization calculation mode, it can't give full play to the resources of the edge device such as computing, storage, etc. Fog computing can improve the resource utilization efficiency of the edge device, and solve the problem about service computing of the delay-sensitive applications. This paper researches on the framework of the fog computing, and adopts Cloud Atomization Technology to turn physical nodes in different levels into virtual machine nodes. On this basis, this paper uses the graph partitioning theory to build the fog computing's load balancing algorithm based on dynamic graph partitioning. The simulation results show that the framework of the fog computing after Cloud Atomization can build the system network flexibly, and dynamic load balancing mechanism can effectively configure system resources as well as reducing the consumption of node migration brought by system changes.

158 citations


Authors

Showing all 41904 results

NameH-indexPapersCitations
Zhong Lin Wang2452529259003
Yang Yang1712644153049
Jun Chen136185677368
Jun Lu135152699767
Jie Liu131153168891
Shuai Liu129109580823
Jian Zhou128300791402
Chao Zhang127311984711
Shaobin Wang12687252463
Tao Zhang123277283866
Jian Liu117209073156
Xin Li114277871389
Jianhui Hou11042953265
Hong Wang110163351811
Baoshan Xing10982348944
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023161
2022807
20214,662
20204,369
20194,164
20183,586