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7篇 您的检索式:作者名="QIN WenDa"
    题名 作者 年代 出处 被引量
1Energy-efficient cognitive access approach to convergence communications显示文摘This article studies the cognitive access in convergence communications.Convergence communications provide upper-layer applications with uniform communication service,converging different lower-layer networks into a uniform access pattern such as all-IP communications.As an import access in convergence communications,the cognitive access provides users with a flexible and dynamic access to networks.In this article,we do not only take into account the spectrum usage of convergence communication networks,but also consider theirs energy efficiency.An energy-efficient access algorithm is proposed to improve network performance and efficiency.Different from the existing cognitive access,we regard energy efficiency as the optimal objective to turn the energy-efficient cognitive access into an optimal problem.The collision avoidance and sleeping mechanisms are used to reduce energy consumption and raise network throughput.The utility function is proposed to maximize networks’energy efficiency and then achieve the energy-efficient cognitive access.Simulation results show that the proposed approach is effective and feasible,which can significantly improve networks’energy efficiency.XU ZhengZheng QIN WenDa TANG QingYi JIANG DingDe 2014Science China(Information Sciences)2014,57,4:4
2Interfacial electron rearrangement: Ni activated Ni(OH)_(2) for efficient hydrogen evolution显示文摘The rational modulation of electronic structure is highly desirable to develop an efficient alkaline hydrogen evolution reaction(HER)catalyst for renewable energy applications.Metal hydroxide such as Ni(OH)_(2) has been proven useful for promoting alkaline HER,but the performance remains unsatisfactory.Herein,the electronic structure of Ni(OH)_(2) is modulated by the interfacial electron rearrangement between Ni-Ni(OH)_(2) heterojunction.Combined experiments with DFT simulations,the electrons of Ni species accumulate to the interfacial Ni-Ni(OH)_(2) sites,which modifies the d band center for promoting conversion of hydrogen intermediates and narrows the energy gap for boosting charge transfer in the HER process.Thus,the integrated electrode exhibits an efficient HER performance to drive10 mA cm^(-2) at the overpotential of 72 mV with a low Tafel slope of 43 mV dec^(-1).Our work renders a valuable insight for understanding and rationally designing efficient catalysts in alkaline HER.Wenda Zhong Wenlong Li Chenfan Yang Jing Wu Rong Zhao Memona Idrees Hui Xiang Qin Zhang Xuanke Li 2021Journal of Energy Chemistry2021,30,10:0
3Patterning of large area nanoscale domains in as-grown epitaxial ferroelectric PbTiO_(3)films显示文摘Effective tuning of nanoscale domain structures provides fundamental basis for controlling and engineering of various functionalities in ferroelectric materials.In this work,we demonstrate the precise patterning of nanoscopic domain structures in as-grown epitaxial PbTiO_(3)(PTO)films by merely introducing an ultrathin pre-patterned doping layer(e.g.,Fe-doped PTO).The doping layer can effectively reverse the interfacial built-in bias,consequent to a reversed initial polarization reorientation in the as-grown film,which makes it possible to transfer the nano-patterns in the doping layer into the domain structure of ferroelectric films.For instance,we have successfully fabricated large area ordered array of nanoscale cylindrical domains(downward polarization)embedded in the matrix domain with opposite polarization(upward polarization)in PTO film.These nanoscale cylinder domains also allow deterministic and reversible erasure and creation induced by biased tip scanning.The results provide an effective pathway for on-demand patterning of large area nanoscale domains in the as-grown films,which may find applications in a wide range of nanoelectronic devices.Luyong Zhang Guo Tian Wenda Yang Dongfeng Zheng Chuanjie Lin Jianbiao Xian Yihang Guo Xingchen Zhang Xiuqin Qiu Lanping Zhang Zhen Fan Deyang Chen Zhipeng Hou Minghui Qin Jun-Ming Liu Xingsen Gao 2023Journal of Materiomics2023,9,1:0
4Antigenic Drift of the Hemagglutinin from an Influenza A(H1N1) pdm09 Clinical Isolate Increases its Pathogenicity In Vitro显示文摘The influenza A(H1 N1)pdm09 virus emerged in 2009 and has been continuously circulating in humans for over ten years.Here,we analyzed a clinical influenza A(H1 N1)pdm09-infected patient case hospitalized for two months in Guangdong(from December 14,2019 to February 15,2020).This isolate,named A/Guangdong/LCF/2019(LCF/19),was genetically sequenced,rescued by reverse genetics,and phylogenetically analyzed in the context of other relevant pdm09 isolates.Compared with earlier isolates,this pdm09 virus’s genetic sequence contains four substitutions,S186 P,T188 I,D190 A,and Q192 E,of the hemagglutinin(HA)segment at position 186–192(H3 numbering)in the epitope Sb,and two of which are located at the 190-helix.Phylogenetic analysis indicated that the epitope Sb started undergoing a rapid antigenic change in2018.To characterize the pathogenicity of this novel substitution motif,a panel of reassortant viruses containing the LCF/2019 HA segment or the chimeric HA segment with the four substitutions were rescued.Kinetic growth data revealed that the reassortant viruses,including the LCF/2019 with the PTIAAQE substitution,propagated faster than those rescued ones having the STTADQQ motif in the epitope Sb in Madin-Darby Canine Kidney(MDCK)cells.The HI test showed that the binding activity of escape mutant to 2018 pdm09 sera was weaker than GLW/2018,suggesting that old vaccines might not effectively protect people from infection.Due to the difference in the selection of vaccine strains,people vaccinated in the southern hemisphere could still suffer a severe infection if infected with this antigenic drift pdm09 virus.Lei Xing Yunbo Chen Boqian Chen Ling Bu Ying Liu Zhiqi Zeng Wenda Guan Qigao Chen Yongping Lin Kun Qin Honglin Chen Xilong Deng Xinhua Wang Wenjun Song 2021Virologica Sinica2021,36,5:0
5Structure of plant photosystem I−light harvesting complex I supercomplex at 2.4Å resolution显示文摘Photosystem I(PSI)is one of the two photosystems in photosynthesis,and performs a series of electron transfer reactions leading to the reduction of ferredoxin.In higher plants,PSI is surrounded by four light-harvesting complex I(LHCI)subunits,which harvest and transfer energy efficiently to the PSI core.The crystal structure of PSI-LHCI supercomplex has been analyzed up to 2.6Åresolution,providing much information on the arrangement of proteins and cofactors in this complicated supercomplex.Here we have optimized crystallization conditions,and analyzed the crystal structure of PSI-LHCI at 2.4Åresolution.Our structure showed some shift of the LHCI,especially the Lhca4 subunit,away from the PSI core,suggesting the indirect connection and inefficiency of energy transfer from this Lhca subunit to the PSI core.We identified five new lipids in the structure,most of them are located in the gap region between the Lhca subunits and the PSI core.These lipid molecules may play important roles in binding of the Lhca subunits to the core,as well as in the assembly of the supercomplex.The present results thus provide novel information for the elucidation of the mechanisms for the light-energy harvesting,transfer and assembly of this supercomplex.Jie Wang Long-Jiang Yu Wenda Wang Qiujing Yan Tingyun Kuang Xiaochun Qin Jian-Ren Shen 2021Journal of Integrative Plant Biology2021,63,7:0
6Tailoring synergetic catalytic interface of VPO/Ni_(2)P to boost hydrogen evolution under alkaline conditions显示文摘Design of the catalyst for efficient water dissociation and hydrogen recombination is paramount in enhancement of the alkaline water electrolysis kinetics.Herein,we reported a delicate hierarchical(VO)_(2) P_(2)O_(7)-Ni_(2) P@NF(VPO-Ni_(2) P@NF)hybrid catalyst that operated efficiently in alkaline media.The VPO and Ni_(2) P respectively act as the water dissociation promoter and the hydrogen recombination center,which synergistically propel water adsorption/dissociation and H intermediates recombination.The resulting synergistic interfaces between VPO and Ni_(2) P are verified to afford the catalyst an outstanding performance for hydrogen evolution reaction in alkaline media with an overpotential of 154 mV at 10 mA cm^(-2),Tafel slope of 65 mV dec^(-1),and remarkable durability.Furthermore,the catalyst presents the potential for overall water splitting.This work may shed fresh light on the high-performance electrocatalyst design and the application of VPO on water electrolysis.Wenli Xu Qiqi Li Wenda Zhong Bing Sun Qiang Huang Xu Nan Yinhong Gao Yao Yang Qin Zhang Nianjun Yang Xuanke Li 2022Journal of Energy Chemistry2022,31,2:0
7Creation and erasure of polar bubble domains in PbTiO_(3)films by mechanical stress and light illuminations显示文摘The controllable manipulation of polar topological structures(e.g.skyrmion bubble)in ferroelectric materials have been considered as a cornerstone for future programmable nano-electronics.Here,we present the effective creation and erasure of polar bubble states PbTiO_(3)(PTO)multilayers trigged by mechanical stress and light illumination,respectively.It was found that applying atomic force microscope(AFM)tip force can induced formation of nanoscale bubble domains from the initial monodomain state.Moreover,the created bubble domain can be eliminated by exposure to ultraviolet or infrared light illumination.The above results can be understood by modulation of depolarization screening charges and bias fields,as reflected by scanning Kelvin potential microscopic(SKPM)observations,whereby the flexoelectric effect from the tip force tends to remove the screening charges on top surface and modulate the bias field that favors the formation of bubble state while light illumination tends to recover the screen charges and favor the monodomain state.The results provide a good example for multi-field manipulation of polar topologies,which might create a new avenue towards the immerging new concept electronic devices.Xingchen Zhang Hongying Chen Guo Tian Wenda Yang Zhen Fan Zhipeng Hou Deyang Chen Min Zeng Minghui Qin Jinwei Gao Xingsen Gao Jun-Ming Liu 2023Journal of Materiomics2023,9,4:0
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