The improvement of thermoelectric property of bulk ZnO via ZnS addition: Influence of intrinsic defects

As in any semiconducting solids, intrinsic defects can affect the properties of ZnO, such as the electrical and thermal conductivities. Defect engineering is usually focused on optimizing the materials’ synthesis or annealing parameters, i.e., temperature, atmosphere, etc. Here we report an approach to change the intrinsic defects of ZnO by adding a small amount of ZnS. During the sintering process, ZnS was decomposed. Apart from the formation of SO₂, the decomposed S and Zn can also be simultaneously doped onto O and Zn sites to change the intrinsic defects in ZnO. For instance, some of the S was converted to SO₂ and led to the formation of V_o (oxygen vacancy); meanwhile, Zn may move to the V_Zn (Zn vacancy) site and decrease the concentration of Zn vacancy. Due to the changes in these native defects, the carrier concentration increased and the thermal conductivity decreased when the content of ZnS was increased to x = 0.01. This sample had an optimal zT value, which was twice that of undoped ZnO. However, with further increase in ZnS, the carrier concentration was reduced. These results suggest a method to tune the intrinsic defects of ZnO via doping technology and bring potential opportunities to improve the thermoelectric performance of this oxide.     

Effects of anion and cation doping on the thermoelectric properties of n-type PbS

The PbCl_xS_1-x and Pb_1-xBi_xS (x? =?0–0.05) bulks were fabricated with a facile method of hydrothermal synthesis and microwave sintering, and the effect of anionic and cationic donors on the thermoelectric performance of PbS was investigated. Although Cl^? and Bi³⁺ both effectively improved the thermoelectric properties of n-type PbS, more excellent thermoelectric performance was obtained from Cl^? doped samples because of higher electrical property and lower thermal conductivity at higher temperature (T? >?600?K). The thermoelectric figure of merit (ZT) reaches 1.04 for PbCl_0.015S_0.985 at 800?K and increases with temperature increasing without sign of saturation, which is probably the highest value ever reported for single-phase polycrystalline n-type PbS. The results also indicate that the hydrothermal synthesis and microwave sintering can realize anion doping as well as cation doping for n-type PbS at low cost, and PbS should be a robust alternative for PbTe thermoelectric materials.     

500kV电网线路断路器取消合闸电阻的可行性研究

本从电力系统的运行可靠性出发，对５００ｋＶ电网线路断路器取消合闸电阻的可能性进行了研究，分析了采用合闸电阻与单独采用ＭＯＡ时的操作过电压的差别以及相应的第二代５００ｋＶ线路的操作过电压闪络率。还对取消合闸电阻的条件提出了建议。     

Nonisothermal crystallization behavior of highly exfoliated polypropylene/clay nanocomposites prepared by in situ polymerization

Polypropylene/clay nanocomposites (PPCNs) were prepared via an in situ polymerization method with a Ziegler–Natta/clay compound catalyst in which the MgCl₂/TiCl₄ catalyst was embedded in the clay galleries. The wide‐angle X‐ray diffraction and transmission electron microscopy results showed that the clay particles were highly exfoliated in the polypropylene (PP) matrix. The nonisothermal crystallization kinetics of these PPCNs were investigated by differential scanning calorimetry at various cooling rates. The nucleation activity were calculated by Dobreva's method to demonstrate that the highly dispersed silicate layers acted as effective nucleating agents. The Avrami, Jeziorny, Ozawa, and Mo methods were used to describe the nonisothermal crystallization behavior of the PP and PPCNs. Various parameters of nonisothermal crystallization, such as the crystallization half‐time, crystallization rate constant, and the kinetic parameter F(t), reflected that the highly exfoliated silicate layers significantly accelerated the crystallization process because of its outstanding nucleation effect. The activation energy values of the PP and PPCNs determined by the Kissinger method increased with the addition of the nanosilicate layers. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Thermal oxidation‐induced long chain branching and its effect on phase separation kinetics of a polyethylene blend

Thermal oxidation‐induced long chain branching (LCB) during the molding processes for polyolefin copolymer poly(ethylene‐co‐butene) (PEB) and its blend with another polyolefin copolymer poly(ethylene‐co‐hexene) (PEH/PEB 50/50 blend, denoted as H50) was investigated mainly by rheological measurements. LCB with different levels could be introduced on PEB backbones by changing the molding temperature and/or molding time, which could be sensitively characterized by changes of rheological parameters, that is, storage modulus G′ and complex viscosity η*. Thermal oxidation‐induced LCB of PEB in H50 samples could largely influence the phase separation kinetics. Rheological measurements and phase‐contrast optical microscope observations coherently indicated that thermal oxidation‐induced LCB of PEB more or less retarded the development of phase separation and once it reached a certain level, the reduced chain diffusion even arrested phase separation. The decrease of mass‐averaged molecular mass in H50 with high LCB level was ascribed to the reduced hydrodynamic volume. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Influence of acrylate processing aid‐based ionomer containing lanthanide (La(III)) ion on thermal stability,fusion, transparency and mechanical properties of rigid poly(vinyl chloride)

An acrylate processing aid (ACR)‐based ionomer containing lanthanide (La(III)) ion was synthesized and the influences of the ionomer on thermal stability, fusion time, transparency and tensile properties of rigid poly(vinyl chloride) (PVC) were investigated. Results revealed that the ionomer with a suitable La(III) content behaved as a good stabilizer as well as processing aid to the rigid PVC product. The ionomer could accelerate fusion of PVC much more quickly than ACR because of the strong interaction between La(III) carboxylate and PVC. Moreover, it exhibited a stabilizing efficiency comparable to lanthanum and calcium stearates (LaSt₃ and CaSt₂). The composite stabilizer of ionomer/zinc stearate (ZnSt₂) exhibited an ability to improve initial discoloration better than LaSt₃/ZnSt₂ and CaSt₂/ZnSt₂ because the ionomer could form a complex with ZnSt₂ much more slowly than LaSt₃ and CaSt₂. The compounds stabilized using ionomer/ZnSt₂ exhibited a transparency comparable to those stabilized using organotin or liquid barium/zinc stabilizers, which was much better than those stabilized using LaSt₃/ZnSt₂ and CaSt₂/ZnSt₂. Copyright © 2011 Society of Chemical Industry     

Self-assembled monolayer of designed and synthesized triazinedithiolsilane molecule as interfacial adhesion enhancer for integrated circuit

Self-assembled monolayer (SAM) with tunable surface chemistry and smooth surface provides an approach to adhesion improvement and suppressing deleterious chemical interactions. Here, we demonstrate the SAM comprising of designed and synthesized 6-(3-triethoxysilylpropyl)amino-1,3,5-triazine-2,4-dithiol molecule, which can enhance interfacial adhesion to inhibit copper diffusion used in device metallization. The formation of the triazinedithiolsilane SAM is confirmed by X-ray photoelectron spectroscopy. The adhesion strength between SAM-coated substrate and electroless deposition copper film was up to 13.8 MPa. The design strategy of triazinedithiolsilane molecule is expected to open up the possibilities for replacing traditional organosilane to be applied in microelectronic industry.     

生活垃圾长效治理的日本经验及对上海的启示

日本是垃圾分类水平最高、资源循环利用率最高的国家之一.对日本生活垃圾长效治理机制进行分析与介绍,有助于我国破解生活垃圾"运动式"治理所面临的可持续性难题,推进源头分类,实现从"新时尚"到"好习惯"到"绿色循环低碳发展的转变".     

银耳多糖超声波提取工艺优化及抗BV2细胞炎症的作用研究

以银耳为原料, 采用超声波辅助热水浸提法提取银耳多糖, 以多糖提取率为指标, 以超声波功率、提取料液比、提取温度和提取时间为影响因素, 设计单因素试验, 并通过正交试验得到较佳提取工艺。通过用TRPV1(Transient Receptor Potential Vanilloid1)试剂盒检测了小胶质细胞TRPV1的释放水平, 与脂多糖(Lipopolysaccharide, LPS)对照组相比, 不同质量浓度的银耳多糖组(62.5, 250, 1000 μg/mL)均能不同程度地抑制TRPV1的释放量。说明了银耳多糖对于BV2小胶质细胞炎症具有良好的抑制作用。     

Experimental investigation of liquid water in flow field of proton exchange membrane fuel cell by combining X-ray with EIS technologies

The flow field is a pivotal part to manage the transport of water and gas in proton exchange membrane fuel cell. However, the reported water measurement methods (e.g., X-ray and electrochemical impedance spectroscopy (EIS)) cannot give a comprehensive understanding water distribution in the flow field, resulting in challenges in optimizing the channel design and enhancing fuel cell performance. Therefore, we propose a water measurement method combining the X-ray radiography with EIS to investigate the effect of different operating conditions on the growth law and distribution of liquid water in parallel and serpentine flow fields. The attenuation coefficient of liquid water to X-ray is calibrated with constant tube-current and tube-voltage of X-ray generator. Besides, the parallel flow field with hydrophobic treatment is studied. The results show that the water accumulation of the parallel flow field is far more than the serpentine flow field, and the water content of the middle region is higher than that of other regions in the parallel flow field. Furthermore, operating conditions (cathode inlet gas flow rate, inlet gas humidity, and back pressure) have little effect on the liquid water content of the middle region in the parallel flow field. The polarization curve, EIS result, and X-ray radiography show that the performance and water drainage capacity of the hydrophobic parallel flow field are better than the normal one.