1‐Aza‐15‐Crown‐5 Functionalized Graphene Oxide for 2D Graphene‐Based Li+‐ion Conductor

Attachment of Li⁺ ion on graphene surface to realize Li⁺‐ion conductor is a real challenge because of the weak interaction between the ions and the functional groups of graphene oxide; although, a large number of theoretical results are already available in the literature. To overcome this problem, graphene oxide is functionalized by 1‐aza‐15‐crown‐5, the cage‐like structure containing four oxygens that can bind Li⁺ ion through electrostatic interaction. Li⁺ migration on graphene surface has been investigated using ac relaxation mechanism. Perfect Debye‐type relaxation behavior with β (relaxation exponent) value ≈1 resulting from single ion is observed. The activation energy of Li⁺ migration arising due to cation‐π interaction is found to be 0.37 eV, which agrees well with recently reported theoretical value. It is believed that this study will help to design isolated ion conductors for Li⁺‐ion battery.     

Ultrafine Nanoparticle‐Supported Ru Nanoclusters with Ultrahigh Catalytic Activity

The design of an ideal heterogeneous catalyst for hydrogenation reaction is to impart the catalyst with synergetic surface sites active cooperatively toward different reaction species. Herein a new strategy is presented for the creation of such a catalyst with dual active sites by decorating metal and metal oxide nanoparticles with ultrafine nanoclusters at atomic level. This strategy is exemplified by the design and synthesis of Ru nanoclusters supported on Ni/NiO nanoparticles. This Ru‐nanocluster/Ni/NiO‐nanoparticle catalyst is shown to exhibit ultrahigh catalytic activity for benzene hydrogenation reaction, which is 55 times higher than Ru–Ni alloy or Ru on Ni catalysts. The nanoclusters‐on‐nanoparticles are characterized by high‐resolution transmission electron microscope, Cs‐corrected high angle annular dark field‐scanning transmission electron microscopy, elemental mapping, high‐sensitivity low‐energy ion scattering, and X‐ray absorption spectra. The atomic‐scale nanocluster–nanoparticle structural characteristics constitute the basis for creating the catalytic synergy of the surface sites, where Ru provides hydrogen adsorption and dissociation site, Ni acts as a “bridge” for transferring H species to benzene adsorbed and activated at NiO site, which has significant implications to multifunctional nanocatalysts design for wide ranges of catalytic reactions.     

Porous Hybrid Composites of Few‐Layer MoS2 Nanosheets Embedded in a Carbon Matrix with an Excellent Supercapacitor Electrode Performance

Porous hierarchical architectures of few‐layer MoS₂ nanosheets dispersed in carbon matrix are prepared by a microwave‐hydrothermal method followed by annealing treatment via using glucose as C source and structure‐directing agent and (NH₄)₂MoS₄ as both Mo and S sources. It is found that the morphology and size of the secondary building units (SBUs), the size and layer number of MoS₂ nanosheets as well as the distribution of MoS₂ nanosheets in carbon matrix, can be effectively controlled by simply adjusting the molar ratio of (NH₄)₂MoS₄ to glucose, leading to the materials with a low charge–transfer resistance, many electrochemical active sites and a robust structure for an outstanding energy storage performance including a high specific capacitance (589 F g⁻¹ at 0.5 A g⁻¹), a good rate capability (364 F g⁻¹ at 20 A g⁻¹), and an excellent cycling stability (retention 104% after 2000 cycles) for application in supercapacitors. The exceptional rate capability endows the electrode with a high energy density of 72.7 Wh kg⁻¹ and a high power density of 12.0 kW kg⁻¹ simultaneously. This work presents a facile and scalable approach for synthesizing novel heterostructures of MoS₂‐based electrode materials with an enhanced rate capability and cyclability for potential application in supercapacitor.     

An Atomistic Tomographic Study of Oxygen and Hydrogen Atoms and their Molecules in CVD Grown Graphene

The properties and growth processes of graphene are greatly influenced by the elemental distributions of impurity atoms and their functional groups within or on the hexagonal carbon lattice. Oxygen and hydrogen atoms and their functional molecules (OH, CO, and CO₂) positions' and chemical identities are tomographically mapped in three dimensions in a graphene monolayer film grown on a copper substrate, at the atomic part‐per‐million (atomic ppm) detection level, employing laser assisted atom‐probe tomography. The atomistic plan and cross‐sectional views of graphene indicate that oxygen, hydrogen, and their co‐functionalities, OH, CO, and CO₂, which are locally clustered under or within the graphene lattice. The experimental 3D atomistic portrait of the chemistry is combined with computational density‐functional theory (DFT) calculations to enhance the understanding of the surface state of graphene, the positions of the chemical functional groups, their interactions with the underlying Cu substrate, and their influences on the growth of graphene.     

One‐Pot Synthesis of Tunable Crystalline Ni3S4@Amorphous MoS2 Core/Shell Nanospheres for High‐Performance Supercapacitors

Transition metal sulfides gain much attention as electrode materials for supercapacitors due to their rich redox chemistry and high electrical conductivity. Designing hierarchical nanostructures is an efficient approach to fully utilize merits of each component. In this work, amorphous MoS₂ is firstly demonstrated to show specific capacitance 1.6 times as that of the crystalline counterpart. Then, crystalline core@amorphous shell (Ni₃S₄@MoS₂) is prepared by a facile one‐pot process. The diameter of the core and the thickness of the shell can be independently tuned. Taking advantages of flexible protection of amorphous shell and high capacitance of the conductive core, Ni₃S₄@amorphous MoS₂ nanospheres are tested as supercapacitor electrodes, which exhibit high specific capacitance of 1440.9 F g^?1 at 2 A g^?1 and a good capacitance retention of 90.7% after 3000 cycles at 10 A g^?1. This design of crystalline core@amorphous shell architecture may open up new strategies for synthesizing promising electrode materials for supercapacitors.     

一种互联网视频调度服务器发现方法与应用

通过对互联网视频资源调度的分析与引导,可有效纠正视频资源调度错误、提高用户访问感知、优化网络架构和提升网络运营效率;通过对主流互联网视频网站调度方式的梳理归纳,得出了现阶段互联网视频领域中的DNS解析、HTTP 302跳转等常用调度方式及其主要特征;通过对上述常用视频调度方式的分析,结合抓包等数据分析工具,建立起调度服务器的自动识别模型,并基于该自动识别模型定制开发构建成调度发现装置;将该调度发现装置部署现网中,对主要视频网站进行测试分析,进一步验证了该发现方法的准确性。     

基于双同步斩波模式的LED声控灯驱动电源设计

提出了基于双同步斩波模式的微功耗LED声控灯驱动电源设计方法。该驱动电源用一个单片机控制两个开关管分别为主电源和待机电源提供工作电流。主电源采用全波斩波工作模式为LED灯组提供工作电流;待机电源采用半波斩波工作模式,从而大幅降低了待机功耗。该驱动电源结构简单,可在50~60 Hz频率的180~250 V的宽电压范围内工作,具有恒流驱动功能和微功耗特性,且稳定可靠和较高的性价比。