To further understand the underlying physical mechanisms of dealloying of multiphase alloys and control dissolution processes among different phases, the dealloying behavior of melt-spun Al 40 atom % Cu alloy comprising Al 2 Cu and AlCu intermetallic compounds in a 10 wt % sodium hydroxide ͑NaOH͒ aqueous solution was studied. The microstructure of as-dealloyed samples was characterized using x-ray diffraction, scanning electron microscopy, and energy dispersive x-ray analysis. The experimental results show that the alloy with the amount of Al 2 Cu comparable to that of AlCu can be partially dealloyed, which eventually results in the formation of a unique kind of nanoporous copper/AlCu composite. Additionally, the formation mechanism has been well established to describe the morphology and composition evolutions during the dealloying process based upon kinetic competitions between dissolution of Al atoms and diffusion-rearrangement of Cu atoms, which includes three stages, sequentially, defined as "Al 2 Cu dealloying," "AlCu dealloying," and "coarsening accompanying underlying AlCu re-dealloying." © 2010 The Electrochemical Society. ͓DOI: 10.1149/1.3511771͔ All rights reserved.Manuscript submitted September 13, 2010; revised manuscript received October 13, 2010. Published December 16, 2010 Nanoporous metals with large surface area have recently attracted considerable interest in a wide variety of applications including catalysis, sensors, actuators, fuel cells, microfluidic flow controllers, and so forth.1-4 For a long time, template methods are commonly used to fabricate these materials through the replication of porous alumina or liquid-crystal templates. [5][6][7] Because it has been found that dealloying can be used to yield a broad range of porous metals, during recent decades, a great deal of effort has been directed toward the investigation of nanoporous metals prepared through dealloying. [8][9][10][11] However, most of the previously reported porous metals were fabricated by dealloying from binary/ternary alloy systems with a single-phase solid solubility across all compositions, which refer to selective dissolution of one or more active components out of an alloy, such as Cu-Pt, Ag-Au, Cu-Au, and Au-Ag-Pt. [12][13][14][15] In view of their industrial applications, widespread uses of a dealloying technique to make nanoporous metals are frequently hindered by the high cost of these noble metals and limited alloy systems. Thus, the fabrication of nanoporous materials from alloy families based on common metals with multiple phases urgently needs to be investigated.However, a few substantial researches have so far focused on this topic using an electrochemical/chemical dealloying technique because of the difficulties in clarifying dealloying behavior and controlling the dissolution process among different phases in multiphase alloys. 16 Recently, Qi et al. 17 reported that the uniform nanoporous copper ͑NPC͒ with a pore size of several hundred nanometers can be synthesized from dual-phase Al-Cu alloys with a ...
Well-aligned TiO2 nanotube arrays were fabricated from anodization by a subsequent heat treatment. Rate performance and electrochemical properties of TiO2 nanotube arrays were studied intensively. The electrode exhibits excellent rate capabilities at various rates with an average coulombic efficiency reaching 95.6%. It is obvious that TiO2 nanotube array possesses high rate capability and excellent cycling stability.
Solid polymer electrolytes (SPEs) which were composed of poly (ethylene oxide) (PEO), poly (lithium acrylate) (PLiAA), and LiClO4were prepared in order to investigate the influence of LiClO4content on the ionic conductivity of the electrolyte. All of the membranes were investigated by XRD, DSC, and EIS, et.al. The dependence of SPEs conductivity on temperature was measured, and the maximum ionic conductivity is 5.88×10-6S/cm at 293 K for membrane which is composed of PEO+PLiAA+15wt% LiClO4. The electrochemical stability window of the PEO+PLiAA+15wt% LiClO4is 4.75 V verse Li.
The Li/S polymer secondary batteries presents higher capacity, lower materials cost and much better performance in higher operation temperature. A nano-scale sulfur polymer composite cathode material has been developed for these batteries, and its cycle capacity is over 700mAh/g when the lithium metal is used as the anode; A nano-scale Cu/Sn alloy powder has been synthesized by a novel micro-emulsion process, its cycle capacity is over 300 mAh/g; The performance of PVdF gel electrolyte has been improved through the addition of the nanometer SiO2 synthesized in-situ. The advanced Li/S polymer secondary batteries will be a promising alternative for next generation energy storage system.
Tin nano-spheres film was synthesized by electrodeposition based on the copper-nickel nano-pillars which were prepared by electrochemical method on the copper foil in an aqueous solution containing Cu (II) and Ni (II) at room temperature. The morphology, structure and composition of the as-prepared copper-nickel nano-pillars and tin nano-spheres were characterized by SEM, XRD, and EDS. The tin nano-spheres film anode features the large surface area, good electronic conductivity, and adhesion with the current collector, leading to the enhanced performance in lithium-ion batteries.
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