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61.
A novel nonlinear optical (NLO) material Na5Sc(CO3)4·2H2O has been synthesized under a subcritical hydrothermal condition. The structure is determined by single-crystal X-ray diffraction and further characterized by TG analyses and UV–vis–NIR diffuse reflectance spectrum. It crystallizes in the tetragonal space group P-421c, with a = b = 7.4622(6) Å, C = 11.5928(15) Å. The Second-harmonic generation (SHG) on polycrystalline samples was measured using the Kurtz and Perry technique, which indicated that Na5Sc(CO3)4·2H2O was a phase-matchable material, and its measured SHG coefficient was about 1.8 times as large as that of d36 (KDP). The results from the UV–vis diffuse reflectance spectroscopy study of the powder samples indicated that the short-wavelength absorption edges of Na5Sc(CO3)4·2H2O is about 220 nm, suggesting that this crystal is a promising UV nonlinear optical (NLO) materials. 相似文献
62.
63.
Core–Shell Carbon‐Coated CuO Nanocomposites: A Highly Stable Electrode Material for Supercapacitors and Lithium‐Ion Batteries 下载免费PDF全文
Dr. Tao Wen Dr. Xi‐Lin Wu Dr. Shouwei Zhang Prof. Xiangke Wang Prof. An‐Wu Xu 《化学:亚洲杂志》2015,10(3):595-601
Herein we present a simple method for fabricating core–shell mesostructured CuO@C nanocomposites by utilizing humic acid (HA) as a biomass carbon source. The electrochemical performances of CuO@C nanocomposites were evaluated as an electrode material for supercapacitors and lithium‐ion batteries. CuO@C exhibits an excellent capacitance of 207.2 F g?1 at a current density of 1 A g?1 within a potential window of 0–0.46 V in 6 M KOH solution. Significantly, CuO electrode materials achieve remarkable capacitance retentions of approximately 205.8 F g?1 after 1000 cycles of charge/discharge testing. The CuO@C was further applied as an anode material for lithium‐ion batteries, and a high initial capacity of 1143.7 mA h g?1 was achieved at a current density of 0.1 C. This work provides a facile and general approach to synthesize carbon‐based materials for application in large‐scale energy‐storage systems. 相似文献
64.
《Journal of Energy Chemistry》2017,26(6):1140-1146
A binder-free Ir-dispersed ordered mesoporous carbon(Ir-OMC) catalytic electrode has been prepared through a designed in-situ carbonization method, which involves coating resorcinol and formaldehyde mixtures with iridium precursors onto the three-dimensional nickel foam framework, followed by insitu calcination in N_2 atmosphere at 800 ℃ for 3 h. This electrode shows a large surface area, ordered mesoporous structure and homogeneous distribution of metal nanoparticles. It presents good activity and stability towards hydrogen evolution reaction, which is attributed to the efficient mass and electron transport from the intimate contact among Ir nanoparticles, ordered mesoporous carbon matrix and 3 D conductive substrate. We hope that this in-situ carbonization synthetic route can also be applied to design more high-performance catalysts for water splitting, fuel cells and other clean energy devices. 相似文献
65.
Rod-shaped mesoporous silica nanoparticles (RMSN) with built-in gold nanoparticles or thin gold nanowires in the pore channels were in situ synthesized via a one-step procedure. The insertion of a hydrophobic gold precursor into the mesopores of RMSN was reached through a micellar solubilization mechanism and gold nanoparticles were achieved through a thermal reduction. The resulting RMSN and Au-RMSN samples were characterized by using X-ray diffraction, transmission and scanning microscopies (TEM and SEM), X-ray photoelectron spectroscopy (XPS), nitrogen physisorption and solid-state Nuclear Magnetic Resonance (NMR). The interaction of Au precursor (a carbene complex) with the thiol group at the silica surface was identified and found to play a crucial role in the dispersion of the uniform metal nanoparticles at the internal surface of RMSN. Moreover, TEM micrographs revealed the absence of large gold particles outside the mesopore network. The shape of Au nanoparticles and their loading amount in the mesoporous silica could be easily tuned by altering the concentration of gold precursor. 相似文献
66.
The physical properties, namely structural, mechanical, and thermodynamic properties, of Pd2Al intermetallic compound were explored through first-principles calculations within the framework of density functional theory. The calculated lattice constants were consistent with the available experimental data. The calculated elastic constants revealed that Pd2Al was mechanically stable. By the predicted elastic constants, several related properties, namely Cauchy pressures, shear anisotropy factors, directional Young's modulus, bulk, shear and Young's moduli, the ratio of K/G, Vickers hardness, sound velocity, and minimum thermal conductivity for Pd2Al were evaluated. According to the calculated results, it was found that Pd2Al possesses a highly anisotropic feature and behaves in a ductile manner with low stiffness. Finally, temperature-dependence of thermodynamic properties, namely Debye temperature and heat capacity, were also evaluated through the quasi-harmonic Debye model. 相似文献
67.
A series of yellow-emitting oxynitride Ca0.65Si10Al2O0.7N15.3:xEu2+ phosphors with α-sialon structure were synthesized. The phase composition and crystal structure were identified by X-ray diffraction and the Rietveld refinement. The excitation and emission spectra, reflectance spectra and thermal stability were investigated in detail, respectively. Results show that Ca0.65Si10Al2O0.7N15.3:0.12Eu2+ phosphors can be efficiently excited by UV-Vis light in the broad range of 290–450 nm and exhibit broad emission spectra peaking at 550–575 nm. The concentration quenching mechanism are discussed in detail and determined to be the dipole-dipole interaction. When the temperature increased to 150 °C, the emission intensity of Ca0.65Si10Al2O0.7N15.3:0.12Eu2+ phosphor is 88.46% of the initial value at room temperature. White LED was fabricated with N-UV LED chip combined with blue Ca3Si2O4N2:Ce3+ and yellow Ca0.65Si10Al2O0.7N15.3:Eu2+ phosphors. The color rendering index and correlated color temperature of this white LED were measured to 78.94 and 6728.12 K, respectively. All above results demonstrate that the as-prepared Ca0.65Si10Al2O0.7N15.3:xEu2+ may serve as a potential yellow phosphor for N-UV w-LEDs. 相似文献
68.
On the basis of the mineral banalsit (BaNa2Al4Si4O16) and the addition of small B2O3 concentrations, transparent glasses were prepared. Furthermore, in order to achieve nucleation, LiF and CaF2 were added. Hexacelsian was formed in bulk crystallized glass samples whereas, monocelsian, as well as small quantities of nepheline and banalsite were crystallized from sintered glass powder. The scanning electron micrographs of the sintered samples show high crystallinity and crystals with sizes from nano to micrometers. The SEM micrographs and the EDX microanalyses show that nano size rods of monocelsian surrounded by micrometer-sized hexagonal nepheline, banalsite or residual glassy phase occur. The coefficient of thermal expansion of the samples sintered at 1000 °C was higher (12.93–9.52 × 10−6 K−1) in hexacelsian containing samples than in monocelsian (2.24–7.35 × 10−6 K−1) containing ones. The samples also showed notably different densities of 2.6424 and 2.4718 g/cm3, respectively. 相似文献
69.
Carbohydrate components in glycoproteins play a critical role in health and disease and specificity of glycoprotein biomarkers can be greatly enhanced by analysis of their sugar components containing frequently different isomers. We show that two glycan isomers, 2,3-sialyllactose and 2,6-sialyllactose (important in cancer), can be distinguished voltammetrically after their modification with osmium(VI) complexes. Using SWV at different frequencies and CV at different scan rates we found conditions for simple discrimination between these isomers at mercury and carbon electrodes. 相似文献
70.
原创药物的研制得益于蛋白质新靶标的发现,而新靶标的发现依赖于高可信度、高通量的药物-蛋白质相互作用分析方法。蛋白质作为生命功能的执行者,其表达量、空间定位与结构差异直接影响药效的发挥。目前,超过85%的蛋白质尚被认为是无法成药的,主要原因是缺少药物分子靶向的空腔以及相应的反应活性位点。因此,基于蛋白质组学层次实现对氨基酸反应活性位点的表征成为原创共价靶向药物设计的关键,也是克服难以成药靶标蛋白问题的关键。近年来,质谱技术的飞速发展极大地推动了基于蛋白质组学技术的药物-靶蛋白相互作用研究。其中基于活性的蛋白质组分析(ABPP)策略是利用活性位点导向的化学探针分子在复杂样品中实现功能状态酶和药物靶标等蛋白质的检测。基于化学探针的开发和质谱定量技术的发展,ABPP技术在氨基酸反应活性表征研究中展现出重要的应用潜力,将助力于药物新靶标的发现和药物先导化合物的开发。ABPP策略主要基于蛋白质的活性特征进行富集,活性探针作为ABPP策略的核心,近年来取得了飞速进展。该文回顾了ABPP策略的发展历程,重点介绍基于广谱活性探针的ABPP技术在多种氨基酸反应活性筛选领域的研究进展,并对其在药物靶点发现中... 相似文献