Crystal structure and ionic conductivity of Mg-doped apatite-type lanthanum silicates La10Si6-x Mgx O27-x（x=0–0.4）

Lanthanum silicates La10Si6-xMgxO27-x(x = 0–0.4) were prepared by solid state synthesis to investigate the effect of Mg doping on crystal structure and ionic conductivity. Rietveld analysis of the powder XRD patterns reveals that Mg substitution on Si site results in significant enlargement of channel triangles, favoring oxide-ion conduction. Furthermore,an increase of Mg concentration significantly influences the linear density of interstitial oxygen, which plays an important role in ionic conductivity. The Arrhenius plots of La10Si6-xMgxO27-x(x = 0–0.4) suggest that Mg-doped samples present higher conductivity and lower activation energy than non-doped La10Si6O27, and La10Si5.8Mg0.2O26.8exhibits the highest conductivity with a value of 3.0×10-2S ·cm-1at 700?C. Such conductive behavior agrees well with the refined results.The corresponding mechanism has been discussed in this paper.     

High-quality CdS quantum dots sensitized ZnO nanotube array films for superior photoelectrochemical performance

The surface characteristics of ZnO were synthetically optimized by a self-designed simultaneous etching and W-doping hydrothermal method utilizing as-prepared ZnO nanorod (NR) array films as the template. Benefiting from the etching and regrowth process and the different structural stabilities of the various faces of ZnO NRs, the uniquely etched and W-doped ZnO (EWZ) nanotube (NT) array films with larger surface area, more active sites and better energy band structure were used to improve the photoelectrochemical (PEC) performance and the loading quality of CdS quantum dots (QDs). On the basis of their better surface characteristics, the CdS QDs were uniformly loaded on EWZ NT array film with a good coverage ratio and interface connection; this effectively improved the light-harvesting ability, charge transportation and separation as well as charge injection efficiency during the PEC reaction. Therefore, all the CdS QD-sensitized EWZ NT array films exhibited significantly enhanced PEC performance. The CdS/EWZ-7 composite films exhibited the optimal photocurrent density with a value of 12 mA· cm^-2, 2.5 times higher than that of conventional CdS/ZnO-7 composite films under the same sensitization times with CdS QDs. The corresponding etching and optimizing mechanisms were also discussed.     

二次电池研究进展

能源的存储和利用是当今科学和技术发展中的重大课题之一,尤其是作为高效的电能/化学能转化装置的二次电池相关技术一直是科学家研究的热点领域。在此背景下,本文较为系统地介绍目前二次电池的重要研究进展,将从二次电池的发展历史引入,再到其相关的基础理论知识的介绍。随后较为详细地讨论当前不同体系的二次电池及相关应的关键材料的研究进展,涉及到锂离子电池、钠离子电池、钾离子电池、镁离子电池、锌离子电池、钙离子电池、铝离子电池、氟离子电池、氯离子电池、双离子电池、锂-硫(硒)电池、钠-硫(硒)电池、钾-硫(硒)电池、多价金属-硫基电池、锂-氧电池、钠-氧电池、钾-氧电池、多价金属-氧气电池、锂-溴(碘)电池、水系金属离子电池、光辅助电池、柔性电池、有机电池、金属-二氧化碳电池等。此外,也介绍了电池研究中常见的电极反应过程表征技术,包括冷冻电镜、透射电镜、同步辐射、原位谱学表征、磁性表征等。本文将有助于研究人员对二次电池进行全面系统的了解与把握,并为之后二次电池的研究提供很好的指导作用。     

In-situ fabrication of ZnO nanoparticles sensors based on gas-sensing electrode for ppb-level H_2S detection at room temperature

The zinc oxide(ZnO)nanoparticles(NPs)sensors were prepared in-situ on the gas-sensing electrodes by a one-step simple sol-gel method for the detection of hydrogen sulfide(H₂S)gas.The sphere-like ZnO NPs were characterized by scanning electron microscopy(SEM),transmission electron microscopy(TEM),x-ray diffraction(XRD),energy dispersive x-ray analysis(EDX),and their H₂S sensing performance were measured at room temperature.Testing results indicate that the ZnO NPs exhibit excellent response to H₂S gas at room temperature.The response value of the optimal sample to750 ppb H₂S is 73.3%,the detection limit reaches to 30 ppb,and the response value is 7.5%.Furthermore,the effects of the calcining time and thickness of the film on the gas-sensing performance were investigated.Both calcining time and film thickness show a negative correlation with the H₂S sensing performance.The corresponding reaction mechanism of H₂S detection was also discussed.     

多尺度有限元法结合分层网格模拟二维奇异摄动的两端边界层问题

通过摄动系数建立分层网格,用多尺度有限元法捕捉对流扩散方程的两端边界层,研究二维奇异摄动模型。基于分层网格并利用多尺度基函数刻画了边界层的微观信息,用有限的计算资源、较短的计算时间, 得到了不依赖于摄动系数、一致稳定的模拟结果。     

Crystal structure and ionic conductivity of Mg-doped apatite-type lanthanum silicates LaloSi6-xMgxO27-x （x= 0-0.4）

Lanthanum silicates LaloSi6 xMgxO27_x （x = 0-0.4） were prepared by solid state synthesis to investigate the effect of Mg doping on crystal structure and ionic conductivity. Rietveld analysis of the powder XRD patterns reveals that Mg substitution on Si site results in significant enlargement of channel triangles, favoring oxide-ion conduction. Furthermore, an increase of Mg concentration significantly influences the linear density of interstitial oxygen, which plays an important role in ionic conductivity. The Arrhenius plots of LaloSi6_xMgxO27 x （x = 0-0.4） suggest that Mg-doped samples present higher conductivity and lower activation energy than non-doped La10Si6027, and LaloSis.8Mgo.2026.8 exhibits the highest conductivity with a value of 3.0× 10-2 S .cm 1 at 700 ℃. Such conductive behavior agrees well with the refined results. The corresponding mechanism has been discussed in this paper.     

三维荧光光谱技术在溶解有机质-吸附态砷相互作用中的应用进展

溶解有机质使含砷矿物还原溶解是地下水中砷富集的因素之一,三维荧光光谱技术可以进一步研究溶解有机质在砷迁移过程中的多重作用。本文从溶解有机质的组分、荧光特征指数以及荧光猝灭三个方面综述了三维荧光光谱技术在溶解有机质-砷相互作用中的应用。溶解有机质中的腐殖质组分会与砷形成络合物促进砷向地下水中迁移,还原性醌类充当电子穿梭体,增强了砷在水中的迁移性能。通过荧光指数、腐殖化指数和氧化还原指数可以判断溶解有机质的来源、腐殖化程度以及氧化还原态组分。地表水中砷浓度低,荧光指数高,腐殖化指数较低且以腐殖质物质为主;地下水中砷浓度和腐殖化指数较高,荧光指数低,且腐殖质的醌类部分较少,表明随着水中砷浓度升高,荧光指数成下降趋势,地表水中的腐殖质醌类充当电子穿梭加强了氧化铁的还原和砷迁移作用,促进地表水中的砷向地下水中迁移。砷和溶解有机质会形成砷-溶解有机质络合物,使溶解有机质发生荧光猝灭。pH值和金属离子会影响溶解有机质和砷的络合,但pH值主要影响溶解有机质自身的荧光强度,对砷-溶解有机质络合物的荧光强度影响不大,Ca²⁺能够明显增强溶解有机质-砷的类蛋白荧光。     

多尺度有限元结合Bakhvalov-Shishkin网格法高效处理边界层问题

提出了用多尺度有限元逼近法来模拟奇异摄动的对流扩散边界层问题.通过求解基于微分算子的子问题获得的多尺度基函数来有效捕获边界层的局部信息,用改良的Bakhvalov Shishkin（B-S）网格来求解奇异摄动的对流扩散边界层问题,可实现高效逼近.与传统有限元法相比,多尺度有限元法占用的计算资源和存储空间较少,利用B-S粗网格就可得到不依赖于小参数ε、精度很高的2阶L2范数的一致超收敛结果.特别当参数ε非常小时,采用多尺度有限元结合B-S网格来求解奇异摄动问题,优势更显著.     

Low-temperature synthesis of apatite-type La_(9.33)Ge_6O_(26) as electrolytes with high conductivity

In the present study,high-quality apatite-type La_(9.33)Ge_6O_(26) powders are successfully synthesized by a facile moltensalt synthesis method(MSSM) at low temperatures,using Li Cl,Li Cl/Na Cl mixture(mass ratio 1:1) as molten salt,respectively.Experimental results indicate that the optimal mass ratio between reactant and molten salt is 1:2,and Li Cl/Na Cl mixed molten-salt is more beneficial for forming high-quality La_(9.33)Ge_6O_(26) powders than Li Cl individual molten-salt.Comparing with the conventional solid-state reaction method(SSRM),the synthesis temperature of apatitetype La_(9.33)Ge_6O_(26) powders using the MSSM decreases more than 350?C,which can effectively avoid Ge loss in the preparation process of precursor powders.Furthermore,the powders obtained by the MSSM are homogeneous,nonagglomerated and well crystallized,which are very favorable for gaining dense pellets in the premise of avoiding Ge loss.On the basis of high-quality precursor powders,the dense and pure ceramic pellets of La_(9.33)Ge_6O_(26) are gained at a low temperature of 1100?C for 2 h,which exhibit higher conductivities(σ850?C(Li Cl)= 2.3 × 10~(-2) S·cm~(-1),σ850 ?C(Li Cl/Na Cl) = 4.9 × 10~(-2) S·cm~(-1)) and lower activation energies(Ea(Li Cl)= 1.02 e V,Ea(Li Cl/Na Cl)= 0.99 e V) than that synthesized by the SSRM.