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排序方式: 共有920条查询结果,搜索用时 140 毫秒
1.
Jinming Wang Meng Yang Guodong Zou Di Liu Qiuming Peng 《Advanced functional materials》2021,31(21):2101180
Lithium (Li) metal, as an appealing candidate for the next-generation of high-energy-density batteries, is plagued by its safety issue mainly caused by uncontrolled dendrite growth and infinite volume expansion. Developing new materials that can improve the performance of Li-metal anode is one of the urgent tasks. Herein, a new MXene derivative containing pure rutile TiO2 and N-doped carbon prepared by heat-treating MXene under a mixing gas, exhibiting high chemical activity in molten Li, is reported. The lithiation MXene derivative with a hybrid of LiTiO2-Li3N-C and Li offers outstanding electrochemical properties. The symmetrical cell assembling lithiation MXene derivative hybrid anode exhibits an ultra-long cycle lifespan of 2000 h with an overpotential of ≈30 mV at 1 mA cm−2, which overwhelms Li-based anodes reported so far. Additionally, long-term operations of 34, 350, and 500 h at 10 mA cm−2 can be achieved in symmetrical cells at temperatures of −10, 25, and 50 °C, respectively. Both experimental tests and density functional theory calculations confirm that the LiTiO2-Li3N-C skeleton serves as a promising host for Li infusion by alleviating volume variation. Simultaneously, the superlithiophilic interphase of Li3N guides Li deposition along the LiTiO2-Li3N-C skeleton to avoid dendrite growth. 相似文献
2.
3.
A kind of complex additive mainly containing Al, Mg, F, and O was prepared. The synthetical performances of the property-modified prebaked anodes containing additives were tested in laboratory. On the basis of ideal testing results obtained, a large number of industrial prebaked property-modified anodes are prepared in a large-scale aluminum company. Further more, they are all used in 160 kA prebaked anode aluminum electrolysis cells. The statistic result show that, compared with common anodes, the property-modified ones enhance current by 11.6 kg per ton aluminum averagely. 相似文献
4.
P.M De CamposA.V Benedetti L.A De FariaV Cardoso J.F.C Boodts 《Electrochimica acta》2002,47(8):1283-1295
Electrodes of RhxTi(1−x)Oy nominal composition were prepared by thermal decomposition of the chloride or nitrate precursor salts dissolved in strongly acidic medium and applied by brush to both sides of a Ti° support. A systematic study of the influence of calcination temperature and time as well as oxygen flux was conducted. The coatings were characterised by SEM, EDAX, XRD, open circuit potential measurements and cyclic voltammetry (CV). Visible-ultraviolet spectrophotometry was employed to identify the chemical form of the precursor in solution while thermogravimetric analysis (TGA) was used to assess the decomposition temperature ranges. Optimisation of the coating preparation parameters showed coatings obtained from [Rh(H2O)6](NO3)3 precursor dissolved in HNO3 1:2 (v/v) and fired at 430 °C for 2 h in a 5 l min−1 oxygen stream-furnished stable electrodes having the highest electrochemically active surface area. 相似文献
5.
V.V. Pani? V.M. Jovanovi? M.W. Barsoum A.B. Dekanski 《Surface & coatings technology》2007,202(2):319-324
Electroactive oxide coatings on titanium, known in industrial chlorine production as dimensionally stable anodes (DSA), are of limited service life owing to the dissolution of active oxide, but also due to low corrosion stability of titanium, at high anodic potentials and elevated temperatures. In order to improve the anode stability, ternary carbide, Ti3SiC2, could be a promising material for the coating support, since chemical corrosion stability of Ti3SiC2 is significantly higher if compared to Ti. In this work, the possibility of the sol-gel preparation of RuO2-TiO2 coating on Ti3SiC2 is investigated and comparison of the basic characteristics of sol-gel processed oxide coating, Ru0.5Ti0.5O2, applied onto Ti3SiC2 and Ti, is reported. Microscopic investigation of the coating surface showed that considerably less cracked coating is formed onto the Ti3SiC2 support. Slightly higher voltammetric currents are registered for Ti3SiC2-supported coating in H2SO4 and NaCl solution. The activity for chlorine evolution is higher, while the currents of oxygen evolution reaction are lower for Ru0.5Ti0.5O2/Ti3SiC2 anode in comparison to Ru0.5Ti0.5O2/Ti anode. Even though these preliminary results on the basic electrochemical properties of Ru0.5Ti0.5O2/Ti3SiC2 anode and chemical stability of Ti3SiC2 are promising, the accelerated stability test in NaCl solution showed that coated Ti3SiC2 is not anodically stable and lasts considerably shorter than Ru0.5Ti0.5O2/Ti anode prepared and tested under the same conditions. 相似文献
6.
把实型铸造与熔铸技术有机结合提出金属基复合材料颗粒强化新技术。通过在实型铸造的泡沫材料的特定部位,事先将高性能合金进行弥散分布处理,浇铸金属母液,在金属结晶凝固过程中,在保持基体材料成分及性能不变的情况下,一次性获得表层或内表层具有特殊性能的金属基复合材料铸件。复合材料层成分、组织由表层向基体呈梯度分布,厚度可控,可以进行机械后加工。 相似文献
7.
Dong-il Shin François Gitzhofer Christian Moreau 《Journal of Thermal Spray Technology》2007,16(1):118-127
Metal-based thermal barrier coatings (MBTBCs) have been produced using high frequency induction plasma spraying (IPS) of iron-based
nanostructured alloy powders. The study of MBTBCs has been initiated to challenge issues associated with current TBC materials
such as difficult prediction of their “in-service” lifetime. Reliability of TBCs is an important aspect besides the economical
consideration. Therefore, the study of MBTBCs, which should posses higher toughness than the current TBC materials, has been
initiated to challenge the mechanical problems of ceramic-based TBCs (CBTBCs) to create a new generation of TBCs. The thermal
diffusivity (TD) (α) properties of the MBTBCs were measured using a laser flash method, and density (ρ) and specific heat
(C
p) of the MBTBCs were also measured for their thermal conductivity (k) calculation (k = αρ
C
p). 相似文献
8.
Bowen Jin Yuanhui Liu Junya Cui Shimeng Zhang Yu Wu Annan Xu Ming Xu Mingfei Shao 《Advanced functional materials》2023,33(31):2301909
Regarding the complex properties of various cations, the design of aqueous batteries that can simultaneously store multi-ions with high capacity and satisfactory rate performance is a great challenge. Here an amorphization strategy to boost cation-ion storage capacities of anode materials is reported. In monovalent (H+, Li+, K+), divalent (Mg2+, Ca2+, Zn2+) and even trivalent (Al3+) aqueous electrolytes, the capacity of the resulting amorphous MoOx is more than quadruple than that of crystalline MoOx and exceeds those of other reported multiple-ion storage materials. Both experimental and theoretical calculations reveal the generation of ample active sites and isotropic ions in the amorphous phase, which accelerates cation migration within the electrode bulk. Amorphous MoOx can be coupled with multi-ion storage cathodes to realize electrochemical energy storage devices with different carriers, promising high energy and power densities. The power density exceeded 15000 W kg−1, demonstrating the great potential of amorphous MoOx in advanced aqueous batteries. 相似文献
9.
Yi Sun Kuanxin Zhang Run Chai Yueda Wang Xianhong Rui Kang Wang Huaxia Deng Hongfa Xiang 《Advanced functional materials》2023,33(36):2303020
Considered the promising anode material for next-generation high-energy lithium-ion batteries, SiOx has been slow to commercialize due to its low initial Coulombic efficiency (ICE) and unstable solid electrolyte interface (SEI) layer, which leads to reduced full-cell energy density, short cycling lives, and poor rate performance. Herein, a novel strategy is proposed to in situ construct an artificial hybrid SEI layer consisting of LiF and Li3Sb on a prelithiated SiOx anode via spontaneous chemical reaction with SbF3. In addition to the increasing ICE (94.5%), the preformed artificial SEI layer with long-term cycle stability and enhanced Li+ transport capability enables a remarkable improvement in capacity retention and rate capability for modified SiOx. Furthermore, the full cell using Li(Ni0.8Co0.1Mn0.1)O2 and a pre-treated anode exhibits high ICE (86.0%) and capacity retention (86.6%) after 100 cycles at 0.5 C. This study provides a fresh insight into how to obtain stable interface on a prelithiated SiOx anode for high energy and long lifespan lithium-ion batteries. 相似文献
10.
Junmin Ge Cunshuang Ma Yanhua Wan Guochuan Tang Hongliu Dai Shuhui Sun Weihua Chen 《Advanced functional materials》2023,33(47):2305803
Phosphorus exhibits high capacity and low redox potential, making it a promising anode material for future sodium-ion batteries. However, its practical applications are confined by poor durability and sluggish kinetics. Herein, an innovative in-situ electrochemically self-driven strategy is presented to embed phosphorus nanocrystal (≈10 nm) into a Fe-N-C-rich 3D carbon framework (P/Fe-N-C). This strategy enables rapid and high-capacity sodium ion storage. Through a combination of experimental assistance and theoretical calculations, a novel synergistic catalytic mechanism of Fe-N-C is reasonably proposed. In detail, the electrochemical formation of Fe-N-C catalytic sites facilitates the release of fluorine in ester-based electrolyte, inducing Na+-conducting-enhanced solid-electrolyte interphase. Furthermore, it also effectively induces the dissociation energy of the P-P bond and promotes the reaction kinetics of P anode. As a result, the unconventional P/Fe-N-C anode demonstrates outstanding rate-capability (267 mAh g−1 at 100 A g−1) and cycling stability (72%, 10 000 cycles). Notably, the assembled pouch cell achieves high-energy density of 220 Wh kg−1. 相似文献