新型熔融碳酸盐燃料电池阴极的制备及其溶解性的研究

以LiNO_3和Co(NO_3)_2·6H_2O为原料,以柠檬酸为燃料,采用燃烧合成法制备了LiCoO_2包覆的多孔NiO阴极。X射线衍射技术(XRD)、X射线能量散射谱(EDAX)和电子显微镜(TEM和SEM)分析表明,NiO颗粒表面的包覆层是由尺寸小于100纳米的LiCoO_2微粒构成,并与NiO颗粒紧密烧结在一起,有效地减少了NiO与熔融碳酸盐的接触面积,降低了氧化镍的溶解度。     

Nanocomposites of CoO and a mesoporous carbon (CMK-3) as a high performance cathode catalyst for lithium-oxygen batteries

A nanocomposite of CoO and a mesoporous carbon (CMK-3) has been studied as a cathode catalyst for lithium-oxygen batteries in alkyl carbonate electrolytes. The morphology and structure of the as-prepared nanocomposite were characterized by field emission scanning electron microscopy, transmission electron microscopy and high resolution transmission electron microscopy. The electrochemical properties of the mesoporous CoO/CMK-3 nanocomposite as a cathode catalyst in lithium-oxygen batteries were studied using galvanostatic charge-discharge methods. The reaction products on the cathode were analyzed by Fourier transform infrared spectroscopy. The CoO/CMK-3 nanocomposite exhibited better capacity retention than bare mesoporous CMK-3 carbon, Super-P carbon or CoO/Super-P nanocomposite. The synergistic effects arising from the combination of CoO nanoparticles and the mesoporous carbon nanoarchitecture may be responsible for the optimum catalytic performance in lithium-oxygen batteries.      

衬底电极对丝网印刷CNT阴极场发射性能的影响

通过丝网印刷技术,将碳纳米管(carbon nanotube,CNT)浆料直接转移到CrCuCr薄膜衬底电极、掺Sn的In_2O_3(indium tin oxides,ITO)透明导电薄膜衬底电极和Ag浆导电厚膜衬底电极上,高温烧结后得到CNT阴极,并对CNT阴极进行表面形貌和场发射性能的研究.结果表明,不同衬底电极对CNT阴极场发射性能的影响不一样,CrCuCr薄膜衬底电极CNT阴极、ITO透明导电薄膜衬底电极CNT阴极及Ag浆厚膜导电衬底电极CNT阴极场发射的开启电场分别为0.99、2.05和2.46V/μm;当电场为3.0V/μm时,它们的亮度分别为2472、1889、587cd/m~2.CrCuCr薄膜衬底电极CNT阴极的场发射性能最优,ITO透明导电薄膜衬底电极CNT阴极次之,Ag浆厚膜导电衬底电极CNT阴极最差,并根据金属-半导体理论模型分析了原因.     

Interfacial scattering at electrochemically fabricated atom-scale junctions between thin gold film electrodes in a microfluidic channel

Atom-scale junctions were formed between two Au thin-film electrodes by a combination of lithography, microfluidics, and electrochemistry. Two Au thin-film electrodes with a small (0.25-25 microm) gap between them were lithographically defined such that the gap fell in the center of a 100-microm-wide microfluidic channel in poly(dimethylsiloxane). Directional electrodeposition between the Au thin-film electrodes, accomplished by applying a potential between the thin-film electrodes, caused Au to etch from the anode and deposit on the cathode, thereby closing the gap. Current through the gap was monitored continuously, and the directional electrodeposition was terminated when a current near that corresponding to the conductance quantum, G(0) = 2e(2)/h, was reached. To regenerate the device, the atom-scale junction was broken with a potential sweep, the microfluidic channel was rinsed, and the junction was re-formed with a subsequent comparator-terminated directional electrodeposition. Alternating current impedance was measured while hexadecanethiol (HDT) was chemisorbed onto the atom-scale junction. The interfacial scattering from chemisorption of the Lewis base HDT on the atom-scale junction caused a normalized impedance change of 71 +/- 1%, the noise level being equivalent to a population fluctuation of five HDT molecules.     

粉末溅射法制备薄膜充电电池材料

经过长时间的研究和探索,在薄膜制作方法上研究开发了粉末磁控溅射镀膜法。利用这种方法,对全固体薄膜充电电池的多种负极活性物质、固体电解质、正极活性物质进行了薄膜材料的制作,得到了很好的结果。粉末溅射法的成功开发,使我们彻底摆脱了昂贵进口块状靶材的束缚,降低了全固体薄膜充电电池的制作成本,为进一步研究全固体薄膜充电电池奠定了坚实的基础。     

Oxygen Vacancy–Rich In‐Doped CoO/CoP Heterostructure as an Effective Air Cathode for Rechargeable Zn–Air Batteries

An efficient and low‐cost electrocatalyst for reversible oxygen electrocatalysis is crucial for improving the performance of rechargeable metal?air batteries. Herein, a novel oxygen vacancy–rich 2D porous In‐doped CoO/CoP heterostructure (In‐CoO/CoP FNS) is designed and developed by a facile free radicals–induced strategy as an effective bifunctional electrocatalyst for rechargeable Zn–air batteries. The electron spin resonance and X‐ray absorption near edge spectroscopy provide clear evidence that abundant oxygen vacancies are formed in the interface of In‐CoO/CoP FNS. Owing to abundant oxygen vacancies, porous heterostructure, and multiple components, In‐CoO/CoP FNS exhibits excellent oxygen reduction reaction activity with a positive half‐wave potential of 0.81 V and superior oxygen evolution reaction activity with a low overpotential of 365 mV at 10 mA cm^?2. Moreover, a home‐made Zn–air battery with In‐CoO/CoP FNS as an air cathode delivers a large power density of 139.4 mW cm^?2, a high energy density of 938 Wh kg_Zn^?1, and can be steadily cycled over 130 h at 10 mA cm^?2, demonstrating great application potential in rechargeable metal–air batteries.     

Facile synthesis of magnesiated alpha-MoO3 and its electrochemical performance in Li-ion batteries

A facile approach has been developed for the synthesis of layered structure of magnesiated alpha-MoO3 based on the precipitation reaction, in which alpha-MoO3 nanoneedles were prepared as intermediates. The layered magnesiated alpha-MoO3 has been characterized by X-ray powder diffraction (XRD) and scanning electron microscopy (SEM). And the electrochemical performance as cathode materials in Li-ion battery shows that the magnesiated alpha-MoO3 had a capacity of 300 mAh x g(-1) at the first discharge and a fairly good cycle performance at the current density of 200 mA x g(-1). The great improvement indicates that the magnesiation method is an effective way to enhance electrochemical performance for the layered cathode materials.     

镍电极的固相掺杂及在非对称电容中的应用

应用CoO、Zn粉对镍电极进行固相掺杂,电极经若干次充放电循环,Co、Zn元 素在Ni(OH)₂颗粒表层以固溶体的形式富集,可优化活性物质表面的组成和结构,提高活性物 质表层的快速反应能力,从而使镍电极更适用于C／Ni(OH)₂非对称电容器体系.实验结果表 明:在高倍率充放电条件下,掺杂10％CoO的镍电极,其容量为未掺杂电极的2倍;用5％的 Zn粉替代部分导电剂Ni粉,镍电极大电流条件下的循环性能和容量性质将明显改善.     

Synthesis and processing of nanostructured WC-Co materials

In this study a novel approach, termed the integrated mechanical and thermal activation (IMTA) process, was used to synthesize nanostructured WC-Co powder. As a result of the integration of mechanical and thermal activation, nanostructured WC-Co powder was synthesized below 1000°C, starting from WO₃, CoO and graphite powder mixtures. Furthermore, consolidation of the nanostructured WC-Co powder via high velocity oxy-fuel (HVOF) thermal spraying and solid state sintering was investigated. The results demonstrated the feasibility of converting the nanostructured WC-Co powder to coatings and bulk components, the properties of which are either comparable to or better than that of the conventional coarse-grained counterparts.     

Rational Construction of Hollow Core‐Branch CoSe2 Nanoarrays for High‐Performance Asymmetric Supercapacitor and Efficient Oxygen Evolution

Metal selenides have great potential for electrochemical energy storage, but are relatively scarce investigated. Herein, a novel hollow core‐branch CoSe₂ nanoarray on carbon cloth is designed by a facile selenization reaction of predesigned CoO nanocones. And the electrochemical reaction mechanism of CoSe₂ in supercapacitor is studied in detail for the first time. Compared with CoO, the hollow core‐branch CoSe₂ has both larger specific surface area and higher electrical conductivity. When tested as a supercapacitor positive electrode, the CoSe₂ delivers a high specific capacitance of 759.5 F g^?1 at 1 mA cm^?2, which is much larger than that of CoO nanocones (319.5 F g^?1). In addition, the CoSe₂ electrode exhibits excellent cycling stability in that a capacitance retention of 94.5% can be maintained after 5000 charge–discharge cycles at 5 mA cm^?2. An asymmetric supercapacitor using the CoSe₂ as cathode and an N‐doped carbon nanowall as anode is further assembled, which show a high energy density of 32.2 Wh kg^?1 at a power density of 1914.7 W kg^?1, and maintains 24.9 Wh kg^?1 when power density increased to 7354.8 W kg^?1. Moreover, the CoSe₂ electrode also exhibits better oxygen evolution reaction activity than that of CoO.     

LiCoO2正极材料的制备技术及其进展

本文综述了LiCoO2固体和LiCoO2薄膜正极材料的制备技术及其进展,介绍了软溶液制备技术(SSP)用于Li-CoO2正极材料制备的优势及动态,展望了今后LiCoO2正极材料制备技术的方向.     

全固态薄膜锂电池及薄膜电极材料研究进展

对全固态薄膜锂电池及其薄膜电极材料的研究进展进行了综述.分析了薄膜锂电池成为发展热点的客观原因;系统归纳了阴极薄膜、电解质薄膜和阳极薄膜材料及其制备技术研究进展;同时,对薄膜锂电池及其电极材料发展前景进行了展望.     

Nanoparticle Cookies Derived from Metal‐Organic Frameworks: Controlled Synthesis and Application in Anode Materials for Lithium‐Ion Batteries

The capacity of anode materials plays a critical role in the performance of lithium‐ion batteries. Using the nanocrystals of oxygen‐free metal‐organic framework ZIF‐67 as precursor, a one‐step calcination approach toward the controlled synthesis of CoO nanoparticle cookies with excellent anodic performances is developed in this work. The CoO nanoparticle cookies feature highly porous structure composed of small CoO nanoparticles (≈12 nm in diameter) and nitrogen‐rich graphitic carbon matrix (≈18 at% in nitrogen content). Benefiting from such unique structure, the CoO nanoparticle cookies are capable of delivering superior specific capacity and cycling stability (1383 mA h g^?1 after 200 runs at 100 mA g^?1) over those of CoO and graphite.     

Synthesis and Electrochemical Properties of Carbon-Mixed LiEr_(0.02)Fe_(0.98)PO_4 Cathode Material for Lithium-ion Batteries

LiEr0.02Fe0.98PO4/C composite cathode was synthesized by a simple solution method with polyethylene glycol (PEG) as the reductive agent and carbon source. The effect of erbium doping on the electrochemical behavior of LiFePO4 was studied in this paper. The samples were characterized by X-ray powder diffraction and scanning electron microscopy and the electrochemical properties were investigated by the charge-discharge test. An initial discharge capacity of 149 mAh·g-1 was achieved for the LiEr0.02Fe0.98PO4/C composite cathode with a rate of 0.1 C. The electronic conductivity of Er doped LiFePO4/C was measured as 10-2 S·cm-1. The results indicated that erbium doping did not destroy the lattice structure of LiFePO4 and enlarge the lattice volume. These changes are beneficial to the improvement of the electrochemical performance of the LiFePO4 cathode.     

Low-voltage thin-film electroluminescent devices with low-resistivity stacked insulators

The characteristics and mechanism of low-voltage-driven thin-film electroluminescent (TFEL) devices with low-resistivity (10(6)-10(7)-Omega cm) SiO(2)/Ta(2) O(5) and Al(2)O(3)/Ta(2)O(5) stacked insulating films have been studied. At 50-Hz sinusoidal wave voltage excitation, the threshold voltage of devices with a ZnS:Mn emitting layer is below 40 V, and the brightness and luminous efficiency are above 1000 cd/m(2) and 4 lm/W, respectively, with 60 V voltage. The characteristics of brightness versus voltage (B-V) curves, integrated charge versus voltage (Q-V) figures, and luminous efficiency versus voltage (eta-V) characteristics are different from conventional devices. The study of a special semiconductor layer-a thin probe-doped layer located at a different part of the pure ZnS layer-has proved that the excitation efficiency is not homogeneous across the emitting layer in this kind of device, and its value decreases from the anode toward the cathode, which is opposite of that made with TFEL devices with high-resistivity insulators. By offering a model of space-charge-limited current, the mechanism of low-voltage-driven thin-film electroluminescence, its optoelectronic characteristics, and the distribution characteristics of excitation efficiency across the emitting layer can be thoroughly explained.     

Removal and degradation of phenol in a saturated flow by in-situ electrokinetic remediation and Fenton-like process.

In this laboratory study, a sandy loam soil saturated with phenol solution was treated by in-situ electrokinetics-Fenton process incorporated with a permeable reactive wall of scrap iron powder (SIP). The soil was contaminated and saturated with aqueous phenol solution of 90-115 mg/kg in concentration. It was then placed in a soil cell. The soil cell was assembled with an anode reservoir and a cathode reservoir at its ends. A bed of SIP (1.05-32.69 g) was inserted in the soil cell at a distance of 5 cm from the anode reservoir compartment. For the test runs, 0.3% H(2)O(2) was used as the anode reservoir fluid, whereas de-ionized water was used as the cathode reservoir fluid. An electric gradient of 1 V/cm was applied to enhance the saturated flow in the soil cell for a period of 10 days. Experimental results have shown that the electroosmotic (EO) flow quantity decreased as the amount of SIP increased. This phenomenon was in good agreement with the results showing the value of EO permeability increased with a decreasing amount of SIP. Results also showed that throughout the test period the cumulative, consumed mass of H(2)O(2) in the anode reservoir increased as the amount of SIP decreased. On the other hand, the cumulative, increased mass of phenol in the cathode reservoir was found to increase with a decreasing amount of SIP. Meanwhile, the residual phenol concentration in the soil cell was found to decrease with a decreasing amount of SIP. When 1.05 g scrap iron powder was used, an overall removal and destruction efficiency of phenol of 99.7% was obtained. Therefore, it is evident that an in-situ combined technology of electrokinetic remediation and Fenton-like process is capable of simultaneously removing and degrading the phenol in a saturated flow.     

A study on selected properties of La1−xSrxCoO3 and its application in sealed CO2 lasers

Samples in the composition series La1–xSrxCoO3 with x=0–0.8 were synthesized, and their crystal structures, conductivities and catalytic activities were studied. When x<0.6, they have a rhombohedrally distorted perovskite structure. When x=0.3–0.5, their conductivities at room temperature are of the order of 103S m-1. When the temperature is higher than 250°C, the catalytic activities of La1–xSrxCoO3 were very high which reaches a maximum for the sample at x=0.3. Cylindrical samples were made from La1–xSrxCoO3 x=0.3 and used as a cathode in sealed CO2 lasers. Compared to the traditional Ag–Cu alloy cathode, the performance of La0.7Sr0.3CoO3 is better. The maximum output of a 1.0 m length laser tube using the new cathode is 53.1 Wm-1.     

High-performance electronics using dense, perfectly aligned arrays of single-walled carbon nanotubes

Single-walled carbon nanotubes (SWNTs) have many exceptional electronic properties. Realizing the full potential of SWNTs in realistic electronic systems requires a scalable approach to device and circuit integration. We report the use of dense, perfectly aligned arrays of long, perfectly linear SWNTs as an effective thin-film semiconductor suitable for integration into transistors and other classes of electronic devices. The large number of SWNTs enable excellent device-level performance characteristics and good device-to-device uniformity, even with SWNTs that are electronically heterogeneous. Measurements on p- and n-channel transistors that involve as many as approximately 2,100 SWNTs reveal device-level mobilities and scaled transconductances approaching approximately 1,000 cm(2) V(-1) s(-1) and approximately 3,000 S m(-1), respectively, and with current outputs of up to approximately 1 A in devices that use interdigitated electrodes. PMOS and CMOS logic gates and mechanically flexible transistors on plastic provide examples of devices that can be formed with this approach. Collectively, these results may represent a route to large-scale integrated nanotube electronics.     

Material selection for thin-film solar cells using multiple attribute decision making approach

This paper presents a material selection approach for selecting absorbent layer material for thin-film solar cells (TFSCs) using multiple attribute decision making (MADM) approach. In this paper, different possible materials for absorbent layer and their properties like band gap, absorption coefficient, diffusion length, thermodynamic compatibility and recombination velocity is taken into consideration and MADM approach is applied to select the best material for thin-film solar cells. It is observed that Copper Indium Gallium Diselinide (CIGS) is the best material for the absorbent layer in thin-film solar cells out of all possible candidates. It was observed that the proposed result is in accordance with the experimental findings thus justifying the validity of the proposed study.     

Cathode Architectures for Rechargeable Ion Batteries: Progress and Perspectives

To satisfy the rising demand for energy, battery electrodes with higher loading, to simultaneously increase areal energy and power, are necessary. Nevertheless, in conventional thin-film electrodes, there is mutual exclusion between energy (capacity) and power. Increasing the thickness of electrodes alone is not feasible since this will lead to reductions in ion-diffusion efficiency, as well as electrode flexibility. To address this difficulty, 3D electrode architectures, especially cathode architectures, are proposed to pave a new path for the design and optimization of battery devices. Recent research suggests that 3D cathode architectures may optimize the configuration and engineering processes of battery technologies. Herein, the state-of-the-art progress of cathode architectures in various rechargeable-ion-battery technologies is summarized. Emphasis is placed on the different architecture strategies, areal loading, and mechanical understanding of 3D electrodes. Upcoming research directions are further outlined for future development in this field.