Global Exponential Stability of Hybrid Non-autonomous Neural Networks with Markovian Switching

Neural Processing Letters - This paper discusses the global exponential stability for a class of hybrid non-autonomous neural networks (HNNNs) with Markovian switching, which includes the factors...     

A Dynamic Programming Framework for Large-Scale Online Clustering on Graphs

Neural Processing Letters - As a fundamental technique for data analysis, graph clustering grouping graph data into clusters has attracted great attentions in recent years. In this paper, we...     

An image segmentation approach on improved implicit surface model in straddle strategy

Multimedia Tools and Applications - At present, some experts and scholars do not explicitly mention the static model in the analysis of the straddle strategy, which leads to the research results...     

A review-driven customer preference measurement model for product improvement: sentiment-based importance–performance analysis

Information Systems and e-Business Management - An increasing number of people use social media to share their consumption experiences. Publicly available online reviews have become a significant...     

Cf/C复合材料与纯铜的胶接辅助钎焊连接

采用胶接辅助钎焊方法,以TiH_2粉为活性元素源,环氧树脂为粘性载体,Ag-Cu共晶合金为钎料,Cu箔为应力缓冲层材料,实现了C_f/C复合材料与纯铜的钎焊连接,结果表明,接头界面处产生TiC,TiCu,Ag(s,s),Cu(s,s)等反应产物,其结构可表示为(C_f/C)/TiC+Ag(s,s)+Cu(s,s)+TiCu/Cu。通过钎焊工艺试验得出,在930℃保温25 min钎焊条件下接头的抗剪强度达到最大值30 MPa。     

二连盆地乌兰花凹陷特低渗安山岩储层的有效性评价

针对二连盆地乌兰花凹陷安山岩储层的特性认识不清、有效储层划分不准确的问题，利用岩心薄片、黏土矿物分析、物性测试以及核磁共振实验等手段开展了岩石储集空间特征、岩石蚀变程度、测井响应特征分析。在此基础上，重点开展了基于核磁共振实验的安山岩储层有效孔隙度计算模型研究，开发了相适应的测井解释评价模块，并结合常规测井和试油结果建立了安山岩储层的分类标准。结果表明：安山岩储集空间具有发育"微孔"、"杏仁孔"双孔隙的特征，且以微孔为主；根据不同蚀变程度所建立的安山岩有效孔隙度计算模型具有很高的精度，平均绝对误差为0.16%，平均相对误差为19.40%；新测井解释储层分类标准在实际应用中与试油结论具有很好的一致性，有利于乌兰花凹陷安山岩有效储层的精确划分，并为该地区开发方案的设计及可采储量评价提供技术支持。     

Reaction environment self-modification on low-coordination Ni2+ octahedra atomic interface for superior electrocatalytic overall water splitting

Large scale synthesis of high-efficiency bifunctional electrocatalyst based on cost-effective and earth-abundant transition metal for overall water splitting in the alkaline environment is indispensable for renewable energy conversion. In this regard, meticulous design of active sites and probing their catalytic mechanism on both cathode and anode with different reaction environment at molecular-scale are vitally necessary. Herein, a coordination environment inheriting strategy is presented for designing low-coordination Ni²⁺ octahedra (L-Ni-8) atomic interface at a high concentration (4.6 at.%). Advanced spectroscopic techniques and theoretical calculations reveal that the self-matching electron delocalization and localization state at L-Ni-8 atomic interface enable an ideal reaction environment at both cathode and anode. To improve the efficiency of using the self-modification reaction environment at L-Ni-8, all of the structural features, including high atom economy, mass transfer, and electron transfer, are integrated together from atomic-scale to macro-scale. At high current density of 500 mA/cm², the samples synthesized at gram-scale can deliver low hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) overpotentials of 262 and 348 mV, respectively.

     

Improved reversible dehydrogenation properties of MgH2 by the synergetic effects of graphene oxide-based porous carbon and TiCl3

In this study, we used a combination of graphene oxide-based porous carbon (GC) and titanium chloride (TiCl₃) to improve the reversible dehydrogenation properties of magnesium hydride (MgH₂). Examining the effects of GC and TiCl₃ on the hydrogen storage properties of MgH₂, the study found GC was a useful additive as confinement medium for promoting the reversible dehydrogenation of MgH₂. And TiCl₃ was an efficient catalytic dopant. A series of controlled experiments were carried out to optimize the sample preparation method and the addition amount of GC and TiCl₃. In comparison with the neat MgH₂ system, the MgH₂/GC-TiCl₃ composite prepared under optimized conditions exhibited enhanced dehydrogenation kinetics and lower dehydrogenation temperature. A combination of phase/microstructure/chemical state analyses has been conducted to gain insight into the promoting effects of GC and TiCl₃ on the reversible dehydrogenation of MgH₂. Our study found that GC was a useful scaffold material for tailoring the nanophase structure of MgH₂. And TiCl₃ played an efficient catalytic effect. Therefore, the remarkably improved dehydrogenation properties of MgH₂ should be attributed to the synergetic effects of nanoconfinement and catalysis.