Layered double hydroxides as electrode materials for flexible energy storage devices

To prevent and mitigate environmental degradation,high-performance and cost-effective electrochemical flexible energy storage systems need to be urgently developed.This demand has led to an increase in research on electrode materials for high-capacity flexible supercapacitors and secondary batteries,which have greatly aided the development of contemporary digital communications and electric vehicles.The use of layered double hydroxides(LDHs)as electrode materials has shown productive results over the last decade,owing to their easy production,versatile composition,low cost,and excellent physicochemical features.This review highlights the distinctive 2D sheet-like structures and electrochemical characteristics of LDH materials,as well as current developments in their fabrication strategies for expanding the application scope of LDHs as electrode materials for flexible supercapacitors and alkali metal(Li,Na,K)ion batteries.

Advances in efficient electrocatalysts based on layered double hydroxides and their derivatives

The explore and development of electrocatalysts have gained significant attention due to their indispensable status in energy storage and conversion systems, such as fuel cells, metal–air batteries and solar water splitting cells. Layered double hydroxides（LDHs） and their derivatives（e.g., transition metal alloys, oxides, sulfides, nitrides and phosphides） have been adopted as catalysts for various electrochemical reactions, such as oxygen reduction, oxygen evolution, hydrogen evolution, and COreduction, which show excellent activity and remarkable durability in electrocatalytic process. In this review, the synthesis strategies, structural characters and electrochemical performances for the LDHs and their derivatives are described. In addition, we also discussed the effect of electronic and geometry structures to their electrocatalytic activity. The further development of high-performance electrocatalysts based on LDHs and their derivatives is covered by both a short summary and future outlook from the viewpoint of the material design and practical application.

The tuning of pore structures and acidity for Zn/Al layered double hydroxides:The application on selective hydrodesulfurization for FCC gasoline

Co–Mo catalysts applied on the hydrodesulfurization（HDS） for FCC gasoline were prepared with Zn–Al layered double hydroxides（LDHs） to improve their performances,and the effects of pore structures and acidity on HDS performances were studied in detail. A series of Zn–Al/LDHs samples with different pore structures and acidities are synthesized on the bases of co-precipitation of OH-,CO2-,Al3＋,and Zn2＋. The neutralization p H is a main factor to affect the pore structures and acidity of Zn–Al/LDHs,and a series of Zn–Al/LDHs with different pore structures and acidities are obtained. Based on the representative samples with different specific surface areas（SBET） and acidities,three Co Mo/LDHs catalysts were prepared,and their HDS performances were compared with traditional Co Mo/Al2O3 catalysts. The results indicated that catalysts prepared with high SBETpossessed high HDS activity,and Br？nsted acid sites could reduce the thiol content in the product to some extent. All the three catalysts prepared with LDHs displayed little lower HDS activity but higher selectivity than Co Mo/Al2O3,and could restrain the reactions of re-combination between olefin and H2 S which could be due to the existence of Br？nsted acid sites.

Structured NiFe catalysts derived from in-situ grown layered double hydroxides on ceramic monolith for CO_(2) methanation

Monolithic catalysts for CO_(2) methanation have become an active research area for the industrial development of Power-to-Gas technology.In this study,we developed a facile and reproducible synthesis strategy for the preparation of structured NiFe catalysts on washcoated cordierite monoliths for CO_(2) methanation.The NiFe catalysts were derived from in-situ grown layered double hydroxides(LDHs)via urea hydrolysis.The influence of different washcoat materials,i.e.,alumina and silica colloidal suspensions on the formation of LDHs layer was investigated,together with the impact of total metal concentration.NiFe LDHs were precipitated on the exterior surface of cordierite washcoated with alumina,while it was found to deposit further inside the channel wall of monolith washcoated with silica due to different intrinsic properties of the colloidal solutions.On the other hand,the thickness of in-situ grown LDHs layers and the catalyst loading could be increased by high metal concentration.The best monolithic catalyst(COR-AluCC-0.5M)was robust,having a thin and well-adhered catalytic layer on the cordierite substrate.As a result,high methane yield was obtained from CO_(2) methanation at high flow rate on this structured NiFe catalysts.The monolithic catalysts appeared as promising structured catalysts for the development of industrial methanation reactor.

Hierarchical molybdenum disulfide nanosheet arrays stemmed from nickel-cobalt layered double hydroxide/carbon cloth for highly-efficient hydrogen evolution reaction

The hierarchical structure of molybdenum disulfide(MoS2)nanosheet arrays stemmed from nickelcobalt layered double hydroxide(NiCo-LDH)/carbon cloth was prepared by growing the MoS_(2) nanosheet arrays onto the NiCo-LDH template which was pre-deposited onto the carbon cloth substrate.In this electrode configuration,carbon cloth is the three dimensional and conductive skeleton;NiCo-LDH nanosheets,as the template,ensure the oriented growth of MoS2 nanosheet arrays.Therefore,more MoS_(2) active sites are exposed and the catalyst exhibits good hydrogen evolution reaction activity.

Rational architecture design of yolk/double-shells Si-based anode material with double buffering carbon layers for high performance lithium-ion battery

Among the many strategies to fabricate the silicon/carbon composite,yolk/double-shells structure can be regarded as an effective strategy to overcome the intrinsic defects of Si-based anode materials for Li-ion batteries(LIBs).Hereon,a facile and inexpensive technology to prepare silicon/carbon composite with yolk/double-shells structure is proposed,in which the double buffering carbon shells are fabricated.The silicon/carbon nanoparticles with core-shell structure are encapsulated by SiO_(2)and external carbon layer,and it shows the yolk/double-shells structure via etching the SiO_(2)sacrificial layer.The multiply shells structure not only significantly improves the electrical conductivity of composite,but also effectively prevents the exposure of Si particles from the electrolyte composition.Meanwhile,the yolk/double-shells structure can provide enough space to accommodate the volume change of the electrode during charge/discharge process and avoid the pulverization of Si particles.Moreover,the as-prepared YDS-Si/C shows excellent performance as anode of LIBs,the reversible capacity is as high as 1066 mA h g^(-1) at the current density of 0.5 A g^(-1) after 200 cycles.At the same time,the YDS-Si/C has high capacity retention and good cyclic stability.Therefore,the unique architecture design of yolk/double-shells for Si/C composite provides an instructive exploration for the development of next generation anode materials of LIBs with high electrochemical performances and structural stability.

Advances in preparation methods and mechanism analysis of layered double hydroxide for lithium-ion batteries and lithium-sulfur batteries

Lithium-ion(Li-ion) battery and lithium-sulfur(Li-S) battery have attracted significant attention as promising components for large-scale energy storage because of high theoretical capacity of Li,excellent energy density or environmental friendness for two kinds of batteries.However,there still exist some respective obstacles for commercial applications,such as limited theoretical capacity,high cost and low conductivity of Li-ion cells or shuttle effect of lithium polysulfides of Li-S cells.As typical twodimensional materials,layered double hydroxides(LDHs) exhibit excellent potential in the field of energy storage due to facile tunability of composition,structure and morphology as well as convenient composite and strong catalytic properties.Consequently,various LDHs toward novel separators or interlayers,cathodes,anodes,and interesting catalytic templates are researched to resolve these challenges.In this review,the recent progress for LDHs applied in Li-ion batteries and Li-S batteries including the synthesis methods,designs and applications is presented and reviewed.Meanwhile,the existing challenges and future perspectives associated with material designs and practical applications of LDHs for these two classes of cells are discussed.WeWe hope that the review can attract more attention and inspire more profound researches toward the LDH-based electrochemical materials for energy storage.

Double-layer microwave absorber of nanocrystalline strontium ferrite and iron microfibers

Microwave absorption properties of the nanocrystalline strontium ferrite （SrFe12O19） and iron （α-Fe） microfibers for single-layer and double-layer structures are investigated in a frequency range of 2 GHz 18 GHz. For the singlelayer absorbers, the nanocrystalline SrFe12O19 microfibers show some microwave absorptions at 6 GHz 18 GHz, with a minimum reflection loss （RL） value of -11.9 dB at 14.1 GHz for a specimen thickness of 3.0 mm, while for the nanocrystalline α-Fe microfibers, their absorptions largely take place at 15 GHz-18 GHz with the RL value exceeding -10 dB, with a minimum .RL value of about -24 dB at 17.5 GHz for a specimen thickness of 0.7 mm. For the doublelayer absorber with an absorbing layer of α-Fe microfibers with a thickness of 0.7 mm and matching layer of SrFe12O19 microfibers with a thickness of 1.3 ram, the minimum RL value is about -63 dB at 16.4 GHz and the absorption band width is about 6.7 GHz ranging from 11.3 GHz to 18 GHz with the RL value exceeding -10 dB which covers the whole Ku-band （12.4 GHz 18 GHz） and 27% of X-band （8.2 GHz 12.4 GHz）.

THE DOUBLE-LAYER STRUCTURE OF THE HADLEY CIRCULATION AND ITS INTERDECADAL EVOLUTION CHARACTERISTICS

Based on the three-pattern decomposition of global atmospheric circulation(TPDGAC), this study investigates the double-layer structure of the Hadley circulation(HC) and its interdecadal evolution characteristics by using monthly horizontal wind field from NCEP/NCAR reanalysis data from 1948—2011. The following major conclusions are drawn: First, the double-layer structure of the HC is an objective fact, and it constantly exists in April,May, June, October and November in the Southern Hemisphere. Second, the double-layer structure is more obvious in the Southern than in the Northern Hemisphere. Since the double-layer structure is sloped in the vertical direction, it should be taken into consideration when analyzing the variations of the strength and location of the center of the HC.Third, the strength of the double-layer structure of the HC in the Southern Hemisphere consistently exhibits decadal variations with a strong, weak and strong pattern in all five months(April, May, June, October, and November), with cycles of 20-30 a and 40-60 a. Fourth, the center of the HC(mean position of the double-layer structure) in the Southern Hemisphere consistently and remarkably shifts southward in all the five months. The net poleward shifts over the 64 years are 5.18°, 2.11°, 2.50°, 1.79° and 5.76° for the five respective months, with a mean shift of 3.47°.

Interlayer distance effects on absorption coefficient and refraction index change in p-type double-δ-doped GaAs quantum wells

In the framework of the Thomas–Fermi(TF) approach, a model for the p-type double-δ-doped(DDD) system in Ga As is presented. This model, unlike other works in the literature, takes into account that the Poisson equation associated with the system is nonlinear. The electronic structure is calculated for heavy and light holes. The changes in the electronic structure result of the distance d between the doped layers are studied. In particular, the relative absorption coefficient as well as the relative refractive index change is calculated as a function of the incident photon energy for heavy holes. The effect of the interlayer distance exhibits, in the absorption coefficient, a red shift of the peak position and a decrease in amplitude when the distance increases. In addition, the relative refractive index change node has a red shift as well as the interlayer distance increases. The calculations show that the effect of the separation between layers has a greater influence on the linear terms. These results are very important for theoretical calculations and engineering of optical and electronic devices based in δ-doped Ga As.

Synthesis of Three-Dimensional Hierarchical Flower-Like Mg–Al Layered Double Hydroxides with Excellent Adsorption Performance for Organic Anionic Dyes

In this work,a facile and effective strategy to prepare three-dimensional(3D)hierarchical flower-like Mg–Al layered double hydroxides(3D-LDH)was developed via a one-step double-drop coprecipitation method usingγ-Al 2O 3particles as a template.The characterization and experimental results showed that the calcined product,3D-LDO,features a large specific surface area of 204.2 m^(2)/g,abundant active sites,and excellent adsorption performance for Congo red(CR),methyl orange(MO),and methyl blue(MB).The maximum adsorption capacities of 3D-LDO for CR,MO,and MB were 1428.6,476.2,and 1666.7 mg/g,respectively;such performance is superior to that of most reported adsorbents.The adsorption mechanism of organic anionic dyes by 3D-LDO was extensively investigated and attributed to surface adsorption,the memory effect of 3D-LDO,and the unique 3D hierarchical flower-like structure of the adsorbent.Recycling performance tests revealed that3D-LDO has satisfactory reusability for the three organic anionic dyes.

Synthesis and Crystal Structure of a New One-dimensional Double Helical-chain Polymer, {Zn(O_2CC_(12)H_8CO_2)(H_2O)}_n

A new zinc polymer, {Zn（O2CC12H8CO2）（H2O）}, or {Zn（DPHA）（H2O）}n （O2CC12H8CO2, DPHA = 1,1′ -biphenyl-2,2′-dicarboxylate dianion） has been synthesized under hydrothermal conditions. The crystal is of monoclinic, space group P21/c with a = 12.8418（5）, b = 5.9505（2）, c = 17.2989（5） A, β = 104.020（2）°, V = 1282.52（8） A^3, C14H10O5Zn, Mr= 323.61, Z = 4, Dc = 1.676 g/cm^3,μ = 1.930 mm^-1, F（000） = 656, R = 0.0766 and wR = 0.1871 for 1775 observed reflections （I 〉 2σ（I））. It consists of Zn2（DPHA）2（H2O）2 units, which are further extended into a one-dimensional double helical-chain polymer via Zn-O bonding. The hydrogen bonding interactions extend the helical chains into a two-dimensional layer structure.

Double-layer indium doped zinc oxide for silicon thin-film solar cell prepared by ultrasonic spray pyrolysis

Indium doped zinc oxide （ZnO：In） thin films were prepared by ultrasonic spray pyrolysis on corning eagle 2000 glass substrate. 1 and 2 at.% indium doped single-layer ZnO：In thin films with different amounts of acetic acid added in the initial solution were fabricated. The 1 at.% indium doped single-layers have triangle grains. The 2 at.% indium doped single-layer with 0.18 acetic acid adding has the resistivity of 6.82 × 10^-3 Ω. cm and particle grains. The doublelayers structure is designed to fabricate the ZnO：In thin film with low resistivity （2.58 × 10^-3 Ω. cm） and good surface morphology. It is found that the surface morphology of the double-layer ZnO：In film strongly depends on the substratelayer, and the second-layer plays a large part in the resistivity of the doublewlayer ZnO：In thin film. Both total and direct transmittances of the double-layer ZnO：In film are above 80% in the visible light region. Single junction a-Si：H solar cell based on the double-layer ZnO：In as front electrode is also investigated.

超高料层双层烧结富氧强化及烟气排放行为研究

针对超高料层双层烧结矿强度低的问题,采用富氧方法强化双层烧结。研究富氧浓度和燃料用量对烧结矿产质量的影响,分析普通双层烧结和富氧强化双层烧结的烧结矿主要矿物组成和微观结构,研究两者烧结烟气中O_(2)、CO_(2)和CO的排放行为。研究结果表明:富氧方法能明显强化超高料层双层烧结,大幅度提高烧结矿成品率和转鼓强度;二次点火后对料层进行富氧,氧气体积分数为25%,烧结矿成品率、转鼓强度、利用系数和固体燃耗分别为69.06%、66.40%、2.09t/(m^(2)∙h)和53.79kg/t,与普通双层烧结指标相比,成品率、转鼓强度和利用系数分别提高4.11%、7.73%、0.18t/(m^(2)∙h),固体燃耗降低3.23kg/t;富氧使烧结矿中磁铁矿氧化充分,铁酸钙大量生成,烧结矿结构均质、紧密;富氧增大烧结烟气O_(2)质量分数,可有效解决下部料层缺氧问题,提高燃料燃烧效率,减少CO排放量。

Numerical Analysis of the Structure of High-Strength Double-Layer Steel Plate Concrete Shaft by Drilling Method of Water-Bearing Weak Rock Formation

In order to ensure the safety of coal mine shaft construction, a double-layer steel plate concrete composite shaft wall structure was proposed. However, fewer studies were conducted on this structure, which made engineers too confused to fully recognize its feasibility of this structure. Hence, based on the previous experimental research on the Taohutu mine construction project in Ordos in Inner Mongolia, this research paper aims to provide a widely deep numerical analysis by the usage of the finite element software, in fact, to establish the corresponding numerical analysis model and make a comparison with the experimental data to get the rationality of the verified model. The influence of the composite characteristics of the steel plate and concrete on the ultimate bearing capacity and stress field of the shaft wall structure is studied here through the method of multi-factor analysis. Also, the optimal design scheme of the double-layer steel plate and concrete composite shaft wall structure is proposed in this research paper.

一种套装式子母弹抛撒用燃气发生器的设计研究

为实现子母弹低过载抛撒功能,设计了一种套装式燃气发生器,通过在燃气发生器燃烧室外增加套装壳体形成降压增容辅助室,从而提高抛撒机构的初始作用容积,以达到降低抛撒过载的目的,并通过仿真和试验手段对基于套装式和典型结构燃气发生器的抛撒机构内弹道性能进行了对比研究。结果表明:在相同抛撒速度下,套装式燃气发生器产生的抛撒过载为16.2g,比典型结构燃气发生器的抛撒过载降低了10.4g,降比约39%,过载降低效果明显。本研究为低过载子弹抛撒用燃气发生器设计提供了新的思路。

双层索系柔性光伏支架结构受力性能研究

目的研究双层索系柔性光伏支架结构在风荷载作用下的静力性能与动力响应。方法采用ABAQUS有限元软件开展双层索系柔性光伏支架结构的静力性能、动力特性、动力响应和风振系数分析,探究了跨度、横向连接系间距以及挠度限值等影响因素对支架结构受力性能的影响。结果结构的风振响应随着跨度的增加而增大;结构跨中挠度及上层索索力随横向连接系间距的增大而增大;增大上层索预应力可以减小结构的动力响应,而下层索预应力过大会导致结构的风振响应增大。结论通过研究给出了双层索系柔性光伏支架结构的风振系数取值范围以及上、下层索的初始预拉力设置建议,可以为其结构抗风设计提供参考。

复合材料双层球壳与环板耦合结构振动特性研究

以一阶剪切变形理论为基础,采用谱几何法对不同边界条件下复合材料双层球壳与环板耦合结构振动特性分析模型进行构建,其中采用人工虚拟弹簧技术模拟耦合结构的边界条件。根据耦合处的连接关系,通过布置耦合弹簧模拟器对子结构之间的耦合关系进行模拟。应用哈密顿原理对复合材料双层球壳与环板耦合结构的特征方程进行推导,对耦合结构的固有特性和稳态响应进行求解。将所得结果与有限元结果进行对比,验证了计算的正确性。分析了几何参数、材料参数对复合材料双层球壳与环板耦合结构振动响应的影响。

双层结构对ZnO TFT稳定性的影响

室温下采用射频磁控溅射方法在SiO_(2)/Si衬底上沉积了单层ZnO薄膜和高氧/低氧双层ZnO薄膜,采用电子束蒸发设备蒸镀Al电极,制备单沟道ZnO TFTs和双层沟道ZnO TFTs。比较两种结构ZnO TFTs的各种性能参数,分析双层结构对TFTs产生的影响。实验结果表明,底部高含氧量ZnO层和顶部低含氧量ZnO层构成了DAL同质结且高氧/低氧薄膜存在载流子浓度产差,利用载流子从高浓度向低浓度扩散的性质,可以填补栅介电层和沟道层之间的界面态缺陷,使器件界面类受主陷阱减少,有效降低TFTs的滞回现象。与单有源层TFTs相比,双沟道层TFTs还具有电学调制作用,其电学性能和稳定性均有明显的提高,得到最佳TFTs的开/关电流比达到3.44×10^(9),亚阈值摆幅为0.68 V/dec,阈值电压偏移为1.2 V。

特厚煤层沿空掘巷围岩支卸协同控制技术

针对特厚煤层小煤柱沿空掘巷大范围塑性全煤巷道锚网索的支护难题,以塔山煤矿8204-2小煤柱工作面为工程背景,采用现场实测、理论分析等方法,揭示了锚杆、锚索对沿空大范围塑性全煤巷道的支护机理。锚杆支护主要作用于浅部二次破碎区煤体,形成浅部连续承载结构;锚索主要作用于深部处于三向受力状态的稳定煤体,形成更大范围的连续稳定承载结构;进一步明确了锚杆、锚索有效长度的计算方法,形成了以高预紧力、高强“锚-网-索”支护为基础,以坚硬顶板井下磨料水射流切顶卸压、巷帮大直径钻孔卸压、底板卸压槽卸压为辅的“支卸协同”小煤柱沿空巷道围岩控制技术体系。工程应用结果表明,试验巷道围岩最大变形量小于700 mm,能够满足使用要求。