Electrodeposited synthesis of self-supported Ni-P cathode for efficient electrocatalytic hydrogen generation

One of the key challenges for electrochemical water splitting is the development of low-cost and efficient hydrogen evolution cathode. In this work, a self-supported Ni-P cathode was synthesized by a facile electrodeposition method. The composition and morphology were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy and transmission electron microscopy. The Ni-P cathode performed low onset over-potential, good catalytic activity and long-term stability under neutral and alkaline conditions. The mechanism of Ni-P electrode for hydrogen production was discussed by electrochemical impedance spectroscopy. The excellent performance of Ni-P cathode was mainly attributed to the synergistic effect of phosphate anions and the self-supported feature.     

鱼腥藻PCC7120染色体MazEF同源基因对asr0757/alr0758的初步研究

鱼腥藻PCC7120染色体上的基因对asr0757/alr0758,经NCBI比对显示其与大肠杆菌中的毒素-抗毒素基因Maz EF具有较高的同源性,且具有毒素-抗毒素系统基因的保守遗传结构,为研究其是否属于Maz EF家族系统基因,构建同时含有asr0757和alr0758基因的双启动子选择性表达载体,先选择性诱导了该基因对的表达,再验证了其表达产物对细菌生长的影响.结果显示:成功诱导表达出了目的蛋白asr0757(13.5KD)和alr0758(17.5KD),当单独诱导asr0757基因表达时,细菌生长状况不受影响,单独诱导alr0758表达时细菌生长明显受到抑制,同时诱导asr0757和alr0758基因时细菌生长恢复正常,说明asr0757/alr0758构成具有生物功能的Maz EF家族系统基因对,具有毒性与抗毒性功能.     

基于混合DBN的海上编队通信链路威胁估计

针对海上编队通信链路威胁估计涉及因素多、知识表示与推理存在不确定性等问题,分析了海上编队通信链路威胁要素,依据要素间因果关系建立了通信链路威胁估计的混合动态贝叶斯网络(DBN)模型,提出了混合DBN模型中连续型网络节点变量的学习方法。仿真分析证实了该方法的有效性和可操作性。     

区域城乡协调发展的综合评价——以宁波为例

城乡之间的协调表现在很多方面.要全面、客观地评价一个地区的城乡协调发展情况,必须建立科学合理的评价指标体系,选择恰当的评价方法.本文结合宁波市的实际情况,讨论了城乡协调发展的内涵和目标,提出了城乡协调发展评价指标体系和方法,揭示了宁波市近年城乡协调发展方面存在的问题和未来可能的变化态势.     

采用双等离子体制备非晶态碳膜的研究

采用直流金属磁过滤阴极真空弧(FCVA)制造出Ti和乙炔(C2H2)气体的双等离子体在单晶硅(100)上制备非晶态碳膜.重点研究了乙炔气体和过滤线圈电流对非晶态碳膜的结构、形貌和机械性能的影响.研究结果表明,薄膜中主要成分是TiC,并以(111)作为主晶向;随着过滤线圈电流的增大,薄膜的晶粒度越来越小;薄膜表面的粗糙度逐渐减小,变得更加平整;薄膜的应力减小,可以下降到2.5 GPa.薄膜的显微硬度和弹性模量随着C2H2体积流qV(C2H2)的增大而降低,硬度和弹性模量分别可以达到33.9 GPa和237.6 GPa.非晶态碳膜的摩擦因数在0.1～0.25之间,大大低于衬底材料单晶硅片的摩擦因数0.6.随着过滤线圈电流增大,摩擦因数减小.     

邻甲苯胺在银纳米棒生长中作用的探讨

探讨了邻甲苯胺在制备银纳米棒中的作用.在邻甲苯胺存在下利用乙醇还原硝酸银制备了银纳米棒.产物经过XRD、TEM表征.对比实验表明不加邻甲苯胺或当邻甲苯胺形成配合物(2-(2-甲基苯基)氨基-4-(2-甲基苯基)亚氨基-2-戊烯)后,在类似条件下得到银纳米粒子.     

Hydroxyl radical electrochemically generated with water as the complete atom source and its environmental application

The most reactive hydroxyl radical （OH） was generated by electrochemical approach with safe water as the complete atom source. The direct evidence for OH formation was obtained by electron spin resonance method. The powerful OH electrochemically generated could effectively degrade organic pollutants and reduce the toxicity of wastewater. Electrochemical disinfection by OH was considerably efficient even without the aid of active chlorine. Bacteria inactivation of 99.99% was achieved for contact time of 30 min and current density of 5 mA·cm^-2, In comparison with active chlorine, OH is rather attractive as a promising environmentally benign disinfectant and opens a new route for microbial inactivation.     

An improved traitor tracing scheme based on bilinear map

T6 et al presented a bilinear-map-based traitor tracing scheme（TSZ scheme） with revocation, but it is a symmetric scheme because it does not provide non-repudiation. In this paper, an improved TSZ scheme was proposed by using oblivious polynomial evaluation （OPE） protocol and service parameters. Under the recondition of general sameness capabilities of both TSZ and improved TSZ scheme, the new scheme adds some advantages such as providing multi-service capability, user＇s non-repudiation and data provider＇s no-framing innocent users. Furthermore, it is also proved to be semantically secure under the decisional bilinear Diffie-Hellman （DBDH problem） assumption.     

New crystal structure of molecular complex 1-piperidine carboxylate-piperidinium-H<Subscript>2</Subscript>O studied by X-ray single crystal diffraction

Piperidine absorbs CO2 and H2O in air to form a molecular complex： piperidium-l-piperidinecarboxylate-H2O. The structure of the complex was characterized by X-ray single crystal diffraction. The crystal structure was determined to be triclinic, space group P1^-with a=0.648 6（8） nm, b=0.809 200） nm, c= 1.357 1（16） nm, a=96.96706）°, β =102.506（15）°,γ=104.202 05）°, Z=2. The complex is stabilized via five hydrogen bonds between the three components, N-O electrostatic interaction and O-O interaction （electron transfer） betweenl-piperidinecarboxylate and H2O. Due to electron transference of carbamate ion, the oxygen atom in water molecule is strongly negatively charged and the O-H bond is considerably shorter than that of the free molecule of water. The formation of the molecular complex is a reversible process and will decompose upon heating. The mechanism of formation and stabilization is further investigated herein.