1. Introduction Metal working industry needs accurate thermo- physical properties of liquid metals and alloys as input data for different simulation routines to im- prove the performance of their products. Within this paper we continue the systematic investigation of the dependence of emissivity of binary alloys on the relative concentration of the constituent elements (for a previous paper see [1]). 2. Experimental method A fast ohmic pulse heating technique is applied to heat metallic wire-s… 相似文献
The interconnecred PtIr alloy nanowires were uniformly deposited on carbon cloth via One-step wet chemistry method, which diameter is averaged to be 5 nm with a length of 50–200 nm. The carbon cloth supported PtIr nanowire assembly (PtIr NA/CC) shows a larger electrochemical active surface area (ECSA) due to its 3D nanostructure and a high CO-resistance as a result from the synergistic effect of PtIr alloy. The PtIr NA/CC exhibits an extremely high mass activity and a reliable long-term stability toward methanol oxidation reaction (MOR). The superior catalytic performance on MOR can match and even surpass those best Pt-based nanowires reported recently in the literature. 相似文献
Aqueous Zinc-ion batteries (ZIBs), using zinc negative electrode and aqueous electrolyte, have attracted great attention in energy storage field due to the reliable safety and low-cost. A composite material comprised of VO2·0.2H2O nanocuboids anchored on graphene sheets (VOG) is synthesized through a facile and efficient microwave-assisted solvothermal strategy and is used as aqueous ZIBs cathode material. Owing to the synergistic effects between the high conductivity of graphene sheets and the desirable structural features of VO2·0.2H2O nanocuboids, the VOG electrode has excellent electronic and ionic transport ability, resulting in superior Zn ions storage performance. The Zn/VOG system delivers ultrahigh specific capacity of 423 mAh·g−1 at 0.25 A·g−1 and exhibits good cycling stability of up to 1,000 cycles at 8 A·g−1 with 87% capacity retention. Systematical structural and elemental characterizations confirm that the interlayer space of VO2·0.2H2O nanocuboids can adapt to the reversible Zn ions insertion/extraction. The as-prepared VOG composite is a promising cathode material with remarkable electrochemical performance for low-cost and safe aqueous rechargeable ZIBs.
Exploring economical, efficient and robust electrocatalysts toward the oxygen evolution reaction (OER) is one of the key issues in water splitting technology. Nanostructure engineering of electrocatalysts and hybridizing active species with a conductive support represent powerful strategies to enhance the electrocatalytic performance. Herein, we report a facile one-step solvothermal method to directly grow 3D CoNi-layered double hydroxide (LDH) flower-like architectures onto porous and conductive Ni foam (NF) substrate (denoted as CoNi-LDH(2:1)@NF hereafter). The flower-like hierarchical architecture of CoNi-LDHs with open configurations endows CoNi-LDH microflowers with sufficient accessible active sites and efficient mass diffusion paths. Moreover, the in situ direct growth manner ensures an intimate contact between the electroactive CoNi-LDHs and NF substrate and thus the charge transfer resistance is reduced. Consequently, the as-formed self-supported and binder-free electrode of CoNi-LDH(2:1)@NF exhibits an outstanding OER performance with a small overpotential of 283 mV at a relatively large current density of 50 mA cm−2 and a remarkable long-term electrochemical durability in 0.1 M KOH solution, holding great promise in practical scale-up water electrolysis. The present study may open a new avenue to design and fabricate cost-effective and high-efficiency electrocatalysts for energy conversion applications. 相似文献
Ni–Ce/γ-Al2O3 catalyst (Ni–Ce-LDH-P) derived from LDHs was synthesized on γ-Al2O3. Plasma technology was employed to its preparation process. Impregnation method and thermal calcination and reduction technology were used to prepare reference catalysts (Ni–Ce-LDH-C, Ni–Ce-P and Ni–Ce-C). CO2 methanation was chosen as the probe reaction. XRD, BET, SEM, TEM and CO2-TPD were used to characterize the microstructure and properties of catalyst. Experimental results showed that Ni–Ce-LDH-P catalyst with smaller Ni size, better Ni dispersion and higher alkalinity exhibited outstanding low-temperature activity at range of 200–350 °C. Characterization results showed that the precursor of Ni–Ce-LDH-P catalyst presented in lamellar shape, inferring the formation of chemical bonds among Ni, Ce and Al (from γ-Al2O3). It is the chemical bonds that improved the dispersion of Ni crystal and the interaction between Ni and γ-Al2O3. Meanwhile, the plasma technology with relatively low temperature prevented the sintering and agglomeration of Ni during the preparation process. Therefore, the excellent performance of Ni–Ce-LDH-P catalyst should be ascribed to the synergy of the unique lamellar structure and the special characteristics of “high energy at relatively low temperature” of plasma technology. 相似文献