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101.
Synergistic effect of functional carbon nanotubes and graphene oxide on the anti‐corrosion performance of epoxy coating 下载免费PDF全文
In this work, we reported the synergistic effect of functional carbon nanotubes (CNTs) and graphene oxide (GO) on the anticorrosion performance of epoxy coating. For this purpose, the GO and CNTs were firstly modified by the 3‐aminophenoxyphthalonitrile to realize the nitrile functionalized graphene oxides (GO‐CN) and carbon nanotubes (CNTs‐CN). As modified GO‐CN and CNTs‐CN were characterized and confirmed by Fourier transform infrared spectroscopy, X‐ray photoelectron spectroscopy, and gravimetric analyzer. It was found that about 19 and 24 wt% of 3‐aminophenoxyphthalonitrile were grafted onto the surface of the GO and CNTs, respectively. The electrochemical impedance spectroscopy results showed that the GO‐CN&CNTs‐CN hybrid materials exhibit a remarkable superiority in enhancing the anticorrosion performance of epoxy coatings. Significant synergistic effect of the lamellar structural GO‐CN and CNTs‐CN on the anticorrosion performance of epoxy composite coatings was designed. Besides, the epoxy coating with 1 wt% of the GO‐CN&CNTs‐CN hybrid exhibited the best anticorrosion performance, in which the impedance showed the largest one (immersion in 3.5 wt% of NaCl solution for 168 hr). Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
102.
《Angewandte Chemie (International ed. in English)》2017,56(46):14749-14752
Low‐valent iron centers are critical intermediates in chemical and bio‐chemical processes. Herein, we show the first example of a low‐valent FeI center stabilized in a high‐valent polyoxometalate framework. Electrochemical studies show that the FeIII‐functionalized molecular vanadium(V) oxide (DMA)[FeIIIClVV12O32Cl]3− (DMA=dimethylammonium) features two well‐defined, reversible, iron‐based electrochemical reductions which cleanly yield the FeI species (DMA)[FeIClVV12O32Cl]5−. Experimental and theoretical studies including electron paramagnetic resonance spectroscopy and density functional theory computations verify the formation of the FeI species. The study presents the first example for the seemingly paradoxical embedding of low‐valent metal species in high‐valent metal oxide anions and opens new avenues for reductive electron transfer catalysis by polyoxometalates. 相似文献
103.
近年来,由于锂资源逐渐紧缺而导致其成本增加,锂离子电池发展受到了限制. 作为一个有潜力的替代者,有着相似电化学机制且成本较低的钠离子电池则发展迅速. 但由于钠离子与锂离子相较有着更大半径,在钠离子脱嵌过程中,对大多数电极材料的晶体结构破坏严重. 因此,开发新型电极材料对钠离子电池的进一步发展尤为重要. 其中,层状钒氧化物作为正极材料被广泛研究. 在这项工作中,作者基于钒氧化物,引入钼元素并与碳复合,首次设计合成了一种新型的碳复合钼掺杂的钒氧化物纳米线电极材料,并获得了优良的电化学性能(在50 mA•g-1的电流密度下,最高放电比容量达135.9 mAh•g-1,并在循环75次后仍有82.6mAh•g-1的可逆容量,容量保持率高达71.8%;在1000mA•g-1的高电流密度下循环并回到50mA•g-1后,可逆放电比容量仍能回复至111.5mAh•g-1). 本工作的研究结果证明,这种具有超大层间距的新型碳复合钼掺杂的钒氧化物纳米线是一种非常有潜力的储钠材料,并且我们的工作为钠离子电池的进一步发展提供了一定的理论基础. 相似文献
104.
Erbo Cheng Shoushuang Huang Dayong Chen Ruting Huang Qing Wang Zhangjun Hu Yong Jiang Zhen Li Bing Zhao Zhiwen Chen 《Acta Crystallographica. Section C, Structural Chemistry》2019,75(7):969-978
Metal oxides have a large storage capacity when employed as anode materials for lithium‐ion batteries (LIBs). However, they often suffer from poor capacity retention due to their low electrical conductivity and huge volume variation during the charge–discharge process. To overcome these limitations, fabrication of metal oxides/carbon hybrids with hollow structures can be expected to further improve their electrochemical properties. Herein, ZnO‐Co3O4 nanocomposites embedded in N‐doped carbon (ZnO‐Co3O4@N‐C) nanocages with hollow dodecahedral shapes have been prepared successfully by the simple carbonizing and oxidizing of metal–organic frameworks (MOFs). Benefiting from the advantages of the structural features, i.e. the conductive N‐doped carbon coating, the porous structure of the nanocages and the synergistic effects of different components, the as‐prepared ZnO‐Co3O4@N‐C not only avoids particle aggregation and nanostructure cracking but also facilitates the transport of ions and electrons. As a result, the resultant ZnO‐Co3O4@N‐C shows a discharge capacity of 2373 mAh g?1 at the first cycle and exhibits a retention capacity of 1305 mAh g?1 even after 300 cycles at 0.1 A g?1. In addition, a reversible capacity of 948 mAh g?1 is obtained at a current density of 2 A g?1, which delivers an excellent high‐rate cycle ability. 相似文献
105.
Redox Controllable Switch of Crystalline Phase and Physical Property in SrVO\begin{document}$_{x}$\end{document} Epitaxial Films 下载免费PDF全文
Xue-jiao Gu Zhen-lin Luo Yong-qi Dong Jing-tian Zhou Han Xu Bin Hong Chen Gao 《化学物理学报(中文版)》2019,32(6):727-730
Transition-metal oxides have attracted much attention due to its abundant crystalline phases and intriguing physical properties. However, some of these compounds are difficult to be fabricated directly in film form due to the ease of valence variation of transition-metal elements. In this work, we reveal the reversible structural transition between SrVO\begin{document}$_3$\end{document} and Sr\begin{document}$_2$\end{document} V\begin{document}$_2$\end{document} O\begin{document}$_7$\end{document} films via thermal treatment in oxygen atmosphere or in vacuum. Based on this, Sr\begin{document}$_2$\end{document} V\begin{document}$_2$\end{document} O\begin{document}$_7$\end{document} epitaxial films are successfully synthesized and studied. Property characterizations show that the semitransparent and metallic SrVO\begin{document}$_3$\end{document} could reversibly switch into transparent and insulating Sr\begin{document}$_2$\end{document} V\begin{document}$_2$\end{document} O\begin{document}$_7$\end{document} , implying potential applications in controllable electronic and optical devices. 相似文献
106.
Yaping Chen Dr. Kun Rui Prof. Jixin Zhu Prof. Shi Xue Dou Dr. Wenping Sun 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(3):703-713
Developing clean and sustainable energies as alternatives to fossil fuels is in strong demand within modern society. The oxygen evolution reaction (OER) is the efficiency-limiting process in plenty of key renewable energy systems, such as electrochemical water splitting and rechargeable metal–air batteries. In this regard, ongoing efforts have been devoted to seeking high-performance electrocatalysts for enhanced energy conversion efficiency. Apart from traditional precious-metal-based catalysts, nickel-based compounds are the most promising earth-abundant OER catalysts, attracting ever-increasing interest due to high activity and stability. In this review, the recent progress on nickel-based oxide and (oxy)hydroxide composites for water oxidation catalysis in terms of materials design/synthesis and electrochemical performance is summarized. Some underlying mechanisms to profoundly understand the catalytic active sites are also highlighted. In addition, the future research trends and perspectives on the development of Ni-based OER electrocatalysts are discussed. 相似文献
107.
Mixed iron and molybdenum oxide catalysts supported on nanostructured silica, SBA-15, were synthesized with various Mo/Fe atomic ratios ranging from 0.07/1.0 to 0.57/1.0. Structural characterization of as-prepared MoxOy_FexOy/SBA-15 samples was performed by nitrogen physisorption, X-ray diffraction, and DR-UV-Vis spectroscopy. Adding molybdenum resulted in a pronounced dispersion effect on supported iron oxidic species. Increasing atomic ratio up to 0.21Mo/1.0Fe was accompanied by decreasing species sizes. Strong interactions between iron and molybdenum during the synthesis resulted in the formation of Fe−O−Mo structure units, possibly Fe2(MoO4)3-like species. Reducibility of MoxOy_FexOy/SBA-15 catalysts was investigated by temperature-programmed reduction experiments with hydrogen as reducing agent. The lower reducibility obtained when adding molybdenum was ascribed to both dispersion and electronic effect of molybdenum. Catalytic performance of MoxOy_FexOy/SBA-15 samples was studied in selective gas-phase oxidation of propene with O2 as oxidant. Adding molybdenum resulted in an increased acrolein selectivity and a decreased selectivity towards total oxidation products. 相似文献
108.
109.
Bineta Keita Essadik Abdeljalil François Girard Sophie Gerschwiler Louis Nadjo Roland Contant Christian Haut 《Journal of Solid State Electrochemistry》1999,3(7-8):446-456
New oxide films have been electrodeposited from [P2Mo18O62]6− by potential cycling in mildly acidic aqueous media. To obtain an adherent and persistent film, it is necessary that more
than six electrons/molecule be fixed on the framework of the heteropolyanion. The film is then studied in pure supporting
electrolyte. In this medium, a remarkable current increase is observed during the potential cycling. Whether the film is deposited
on a glassy carbon electrode or on the gold electrode of an electrochemical quartz crystal microbalance (EQCM), exactly the
same steady current increase up to a maximum is obtained in cyclic voltammetric measurements. The EQCM reveals a steady mass
increase during the continuous cycling of the film in the supporting electrolyte. This behaviour is interpreted as featuring
an irreversible water and electrolyte intake into the film, up to a maximum, after which the phenomena observed during reduction
and oxidation processes are taken as featuring intercalation/deintercalation, respectively. This behaviour is much the same
as described in the literature for WO3 and MoO3 bronzes, except that the present films seem very stable and have shown no tendency to dissolve or deactivate.
Received: 2 December 1998 / Accepted: 26 January 1999 相似文献
110.
Bo-Cheng Wang Likey Chen Kuei-Jen Lee Chang-Yuan Cheng 《Journal of Molecular Structure》1999,469(1-3):127-134
The spectral analysis indicates that all isomers of C60O, C70O and C60O2 have an epoxide-like structure (an oxygen atom bridging across a C–C bond). According to the geometrical structure analysis, there are two isomers of fullerene monoxide C60O (the 5,6 bond and the 6,6 bond), eight isomers of fullerene monoxide C70O and eight isomers of fullerene dioxide C60O2. In order to simulate the real reaction conditions at 300 K, the calculation of the different isomers of C60O, C60O2 and C70O fullerene oxides was carried out using the semiempirical molecular dynamics method with two different approaches: (a) consideration of the geometries and thermodynamic stabilities, and (b) consideration of the ozonolysis mechanism. According to the semiempirical molecular dynamic calculation analysis, the probable product of this ozonolysis reaction is C60O with oxygen bridging over the 6–6 bond (C2v). The most probable product in this reaction contains oxygen bridging across in the upper part of C70 (6–6 bond in C70O-2 or C70O-4) an epoxide-like structure. C60O2-1, C60O2-3 and C60O2-5 are the most probable products for the fullerene dioxides. All of these reaction products are consistent with the experimental results. It is confirmed that the calculation results with the semiempirical molecular dynamics method are close to the experimental work. The semiempirical molecular dynamics method can offer both the reaction temperature effect by molecular dynamics and electronic structure, dipole moment by quantum chemistry calculation. 相似文献