BaFe12−x (Mn0.5Cu0.5Zr)x/2O19 hexaferrites with x=1, 2 and 3 were prepared by sol–gel process. The ferrite powders possess hexagonal shape and are well separated from one another. The powders of these ferrites were mixed with polyvinylchloride (PVC) plasticizer to be converted into a microwave absorbing composite ferrite with a thickness of 1.8 mm. X-ray diffractometer (XRD), scanning electron microscope (SEM), ac susceptometer, vibrating sample magnetometer and vector network analyzer were used to analyze its structure, electromagnetic and microwave absorption properties. The results showed that magnetoplumbite structures for all samples were formed. The sample with higher magnetic susceptibility and coercivity exhibits a larger microwave absorbing ability. Also the present investigation demonstrates that a microwave absorber using BaFe12−x(Mn0.5Cu0.5Zr)x/2O19 (x=2 and 3)/PVC with a matching thickness of 1.8 mm can be fabricated for applications over 15 GHz, with reflection loss more than −25 dB for specific frequencies, by controlling the molar ratio of the substituted ions. 相似文献
In this paper, the LiNi0.5Mn1.5O4 cathode materials of lithium-ion batteries are synthesized by a co-precipitation spray-drying and calcining process. The use of a spray-drying process to form particles, followed by a calcination treatment at the optimized temperature of 750 °C to produce spherical LiNi0.5Mn1.5O4 particles with a cubic crystal structure, a specific surface area of 60.1 m2 g?1, a tap density of 1.15 g mL?1, and a specific capacity of 132.9 mAh g?1 at 0.1 C. The carbon nanofragment (CNF) additives, introduced into the spheres during the co-precipitation spray-drying period, greatly enhance the rate performance and cycling stability of LiNi0.5Mn1.5O4. The sample with 1.0 wt.% CNF calcined at 750 °C exhibits a maximum capacity of 131.7 mAh g?1 at 0.5 C and a capacity retention of 98.9% after 100 cycles. In addition, compared to the LiNi0.5Mn1.5O4 material without CNF, the LiNi0.5Mn1.5O4 with CNF demonstrates a high-rate capacity retention that increases from 69.1% to 95.2% after 100 cycles at 10 C, indicating an excellent rate capability. The usage of CNF and the synthetic method provide a promising choice for the synthesis of a stabilized LiNi0.5Mn1.5O4 cathode material.
Graphical Abstract Micro/nanostructured LiNi0.5Mn0.5O4 cathode materials with enhanced electrochemical performances for high voltage lithium-ion batteries are synthesized by a co-precipitation spray-drying and calcining routine and using carbon nanofragments (CNFs) as additive.
Direct para-selective C–H functionalization of arenes remains a daunting challenge and is still significantly restricted to a few scaffolds. Herein, we report an unprecedented pyridine-based para-directing template (DT) assisted, Pd-catalyzed para-C–H alkenylation of three classes of arenes, i.e. phenylpropanoic acids, 2-phenyl benzoic acids and benzyl alcohols, with a series of alkenes including perfluoroalkenes. Notably, the pyridine-based para-DT could be easily synthesized and readily recycled under mild conditions. These results may find application in rapid construction of para-substituted arenes and stimulate the exploration of novel methods for para-C–H functionalization of arenes.An unprecedented pyridine-based para-directing template (DT) assisted, Pd-catalyzed remote para-C–H alkenylation of three classes of arenes is reported herein.相似文献
Vinyl ethylene carbonate (VEC) is investigated as an electrolyte additive to improve the electrochemical performance of LiNi0.4Mn0.4Co0.2O2/graphite lithium-ion battery at higher voltage operation (3.0–4.5 V) than the conventional voltage (3.0–4.25 V). In the voltage range of 3.0–4.5 V, it is shown that the performances of the cells with VEC-containing electrolyte are greatly improved than the cells without additive. With 2.0 wt.% VEC addition in the electrolyte, the capacity retention of the cell is increased from 62.5 to 74.5 % after 300 cycles. The effects of VEC on the cell performance are investigated by cyclic voltammetry(CV), electrochemical impedance spectroscopy(EIS), x-ray powder diffraction (XRD), energy dispersive x-ray spectrometry (EDS), scanning electron microscopy (SEM), and attenuated total reflectance-Fourier transform infrared (ATR-FTIR). The results show that the films electrochemically formed on both anode and cathode, derived from the in situ decomposition of VEC at the initial charge–discharge cycles, are the main reasons for the improved cell performance. 相似文献
Ultrasmall luminescent gold nanoparticles (AuNPs) with excellent capabilities to cross biological barriers offer great promise in designing intelligent model nanomedicines for investigating structure–property relationships at the subcellular level. However, the strict surface controllability of ultrasmall AuNPs is challenging because of their small size. Herein, we report a facile in situ method for precisely controlling DNA aptamer valences on the surface of luminescent AuNPs with emission in the second near-infrared window using a phosphorothioate-modified DNA aptamer, AS1411, as a template. The discrete DNA aptamer number of AS1411-functionalized AuNPs (AS1411-AuNPs, ≈1.8 nm) with emission at 1030 nm was controlled in one aptamer (V1), two aptamers (V2), and four aptamers (V4). It was then discovered that not only the tumor-targeting efficiencies but also the subcellular transport of AS1411-AuNPs were precisely dependent on valences. A slight increase in valence from V1 to V2 increased tumor-targeting efficiencies and resulted in higher nucleus accumulation, whereas a further increase in valence (e.g., V4) significantly increased tumor-targeting efficiencies and led to higher cytomembrane accumulation. These results provide a basis for the strict surface control of nanomedicines in the precise regulation of in vivo transport at the subcellular level and their translation into clinical practice in the future. 相似文献
Strontium ferrite SrFe12O19 (SrM) thick films have been synthesized using a spinning coating sol–gel process. The coating sol was formed from SrFe12O19 powders dispersed in the strontium ferrite raw sol. XRD, TEM, SEM, vibrating sample magnetometer (VSM) and ac susceptometer were employed to evaluate the structure, composition and magnetic properties of SrFe12O19 thick films. The results indicated that a uniform and crack-free coating of Strontium ferrite with ∼15 μm thickness can be produced with a good deal of consistency. The magnetization hysteresis loops were almost the same for magnetic fields both applied in parallel and perpendicular. 相似文献