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以软件工程学的原理对拉深模CAD系统进行结构化分析、结构化设计和结构化程序设计。利用该方法编制的拉深模CAD系统结构化程度高 ,通用性强 ,便于修改和维护 相似文献
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随着各种云应用的数据规模的增大,越来越多的云服务提供商开始关注跨数据中心的大数据块传输(bulk transfer)。跨数据中心的大数据块传输面临的主要挑战是:如何找到最佳的资源调度算法,在用户指定的时限内,用最少的传输资源将用户的数据传输到指定的地点。文中设计了一种有效的带传输时限(transfer deadlines)的、点到多点(Point-to-MultiPoint,P2MP)的跨数据中心数据传输调度算法MSTB(Multi-Source Tree-Based algorithm)。在多源机制和多播转发树的帮助下,MSTB表现得比现有的最优方法更好。仿真实验结果表明,MSTB可以在保证低传输完成时间和低计算复杂度的同时,增加最高达91%的传输请求接受数,增加最高达54%的有效吞吐量。 相似文献
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Shuyu Chen Xiaoyu Han Yang Cao Weiwei Yi Ying Zhu Xiaoqian Ding Kai Li Jieliang Shen Wenguo Cui Dingqun Bai 《Advanced functional materials》2024,34(1):2308205
Disturbance of spatiotemporal oxygen balance is the main cause of delayed healing or nonhealing of large bone defects. The accurate administration of oxygen to regulate disruptions in the spatiotemporal oxygen equilibrium during 9 h of hypoxia is imperative for bone tissue regeneration. Herein, oxygen-loaded nanobubbles prepared by double emulsification are successfully embedded in GelMA/HepMA microsphere macromolecular meshwork by microfluidic techniques, and a spatiotemporalized hydrogel microsphere is constructed by noncovalently binding bone morphogenetic protein 2 (BMP-2). The spatiotemporalized hydrogel microspheres precisely “remote control” oxygen release by ultrasound in vitro 9 h after bone injury to regulate spatiotemporal oxygen homeostasis disorder, maintain a high level of vascular endothelial growth factor (VEGF) expression, and accelerate bone repair. The spatiotemporalized hydrogel microspheres possess good oxygen-carrying capacity and ultrasonic responsiveness, and the oxygen concentration increases to 1.63, 1.95, 2.11, and 2.29 times under the ultrasound action at different intensities of 1, 2, 3, and 4 W, respectively, providing the conditions for the precise regulation of spatiotemporal oxygen balance disorder by ultrasound. In the in vitro hypoxia model and in vivo rat femoral defect model, the spatiotemporal hydrogel microspheres show good vascularization and osteogenesis capabilities, which provide a new strategy for the clinical treatment of large bone defects. 相似文献
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Yaoyao Chen Liwei Tang Xi Zeng Wuqian Guo Tian Yang Haojie Xu Yi Liu Gaoyang Gou Yue Zhao Junhua Luo Zhihua Sun 《Advanced functional materials》2024,34(17):2311726
Circularly polarized light (CPL) detection has sparked the booming interest for versatile chiral-optoelectronic and spintronic devices. For practical device applications, a large asymmetry factor is required to distinguish the handedness of incent light. However, for most chiral CPL active candidates, the difference in optical density or absorption anisotropy is quite subtle under CPL illumination, resulting in a relatively low asymmetry factor (usually ≤ 0.2). Up to date, it remains extremely challenging to achieve CPL response in the achiral crystals. Inch-size achiral perovskite-type crystals of (IBA)2(EA)2Pb3I10 (IBA = 4-isopropylbenzylammonium, EA = ethylammonium), which holds a promise to distinguish CPL with a large asymmetry factor up to ≈0.56 at 405 nm is presented here. This figure-of-merit is comparable or even superior than most of those chiral counterparts. Further First-principles calculations disclose such CPL-active behaviors of (IBA)2(EA)2Pb3I10 are associated with the splitting of its band spin-degeneracy, induced by the breaking of inversion symmetry and spin-orbital coupling (SOC) effects. As far as it is known, the structural origin of CPL-activities of (IBA)2(EA)2Pb3I10 is completely distinctive from the conventional chiral family, which paves a promising pathway to explore new candidates toward high-performance CPL detection. 相似文献
109.
Tao Yang Zong-Wei Chen Xin-Zheng Yue Qing-Chao Liu Sha-Sha Yi Yong-Fa Zhu 《Advanced functional materials》2024,34(18):2313767
Constructing heterostructural photoanodes is attractive for elevating the photoelectrochemical (PEC) performance, however, it is a long-standing challenge to achieve highly efficient interfacial charge transfer. Herein, a CoFe metal-thiolate framework (CoFe MTF)/Fe2O3 photoanode connected by an interfacial Fe─O─N/S bond is designed to modulate the behavior of charge carriers and improve water oxidation performance. It is disclosed that this interfacial bond functions as a direct charge transfer bridge between shallow trap states of Fe2O3 and CoFe MTF, leading to prolonged carrier recombination lifetimes (85 ns for CoFe MTF/Fe2O3 compared to 37 ns for Fe2O3) and enhanced charge transfer efficiency. Alternatively, a robust interfacial electric field is established in the CoFe MTF/Fe2O3 p–n heterojunction, facilitating efficient charge transfer. As expected, the CoFe MTF/Fe2O3 photoanode exhibits significant enhancement in water oxidation, resulting in a three-fold increase in photocurrent density compared to pristine Fe2O3. This study highlights the significance of designing interfacially bonded heterostructural photoelectrodes to regulate the transfer characters of charge carriers. 相似文献
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