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Vacuum Ultraviolet Free-Electron Laser Photoionization Mass Spectrometry of Alpha-pinene Ozonolysis 下载免费PDF全文
Xiangyu Zang Zhaoyan Zhang Chong Wang Tiantong Wang Huijun Zheng Hua Xie Jiayue Yang Dongxu Dai Guorong Wu Weiqing Zhang Gang Li Xueming Yang Ling Jiang 《化学物理学报(中文版)》2022,35(2):281-288
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Xiaohong Li Haitian Zhang Jiayue Gao Defeng Guo Cuizhuo Yang Lei Xu Baoting Liu Xiangyi Zhang 《Journal of nanoparticle research》2011,13(12):6563-6568
The structure transition of nanoparticles has a significant effect on their practical applications. In this study, the transition
temperature of CdS nanoparticles with the size of 3–5 nm from sphalerite to wurtzite structure is significantly reduced to
150 °C under a high pressure of 1 GPa, much lower than that 300–400 °C for CdS nanoparticles and 600 °C for bulk CdS under
room pressure. The lower transition temperature leads to an ultrafine grain size d = 5 nm for the formed wurtzite phase as compared with that d = 33 nm yielded under room pressure with a similar transition volume fraction of ~80%. The underlying physical mechanism
is discussed. 相似文献
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比较了未氧化处理与经浓硝酸或混酸(浓硫酸与浓硝酸体积比为1∶1)处理后的不同多壁碳纳米管(MWNTs)为载体的Pd催化剂(Pd/MWNTs)对水合肼氧化的电催化性能. 光谱表征和电化学测试结果表明, MWNTs表面不修饰或修饰程度过大都不利于金属Pd纳米粒子的沉积. 浓硝酸处理使MWNTs表面修饰的含氧基团适中, 能够促进负载的Pd纳米粒子均一分布, 因此提高Pd/MWNTs催化剂对水合肼的电催化性能. 相反, 混酸处理使MWNTs表面产生的含氧基团过多, 导致金属Pd纳米粒子部分聚集, 从而降低Pd/MWNTs催化剂对水合肼的电催化性能. 相似文献
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Hongye Zhang Tianhao Ji Linglong Li Xingyi Qi Yifan Liu Jianwang Cai Haiyan Du Jiayue Sun 《Acta Physico》2008,24(4):607-611
Ni-doped anatase TiO2 nanobelts (NBs) with different Ni2+ contents were simply prepared by combining ion-exchange with hydrothermal treatment. They were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR), and magnetic measurement techniques. The results showed that Ni2+ cations doped into the TiO2 lattice and no metallic nickel clusters or nanoparticles could be found. The magnetic results demonstrated that the prepared Ni-doped TiO2 samples had complex magnetic mechanism including room-temperature ferromagnetic and paramagnetic behaviors, and with the increase of Ni2+ content, the magnetization also increased under the same applied field owing to uniform distribution of Ni2+ ions in TiO2 nanobelts. 相似文献
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Microwave-assisted synthesis of SrFe12O19 hexaferrites 总被引:1,自引:0,他引:1
Wang Zhanyong Zhong Liuming Qian Huichun Fang Yongzheng Xu Jiayue 《Journal of magnetism and magnetic materials》2010,322(18):2782-2785
Ultra-fine and homogeneous SrFe12O19 hexaferrites were synthesized by a microwave-assisted calcination route. The calcined precursors were prepared by a sol-gel auto-combustion method using Fe(NO3)3·9H2O, Sr(NO3)2 and citric acid as starting materials. The structures, powder morphology and magnetic properties of the products were characterized by X-ray diffraction, scanning electron microscope and vibrating sample magnetometer. The results showed that microwaves are helpful to reduce the calcination temperature and shorten the calcination time. The ferrites with saturation magnetization, remanence and intrinsic coercivity of 54.80 emu/g, 29.52 emu/g and 5261 Oe, respectively, were obtained in samples calcined at 800 °C for 80 min. 相似文献
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Min Jin Jiayue Xu Xinhua Li Hui Shen Qingbo He 《Crystal Research and Technology》2008,43(10):1074-1077
Novel relaxor ferroelectric crystal 0.93Pb(Zn1/3Nb2/3)O3‐0.07PbTiO3 (PZNT93/7) with dimensions about Ø40× 70 mm3 was obtained by directional solidification technique. The growth defects of the crystal were investigated. Rocking curve analysis revealed the crystalline quality of PZNT93/7 crystal was not perfect and the FWHM value was measured to be about 0.7°. Some pits and oxide particles in micro‐size were formed in the crystal due to the growth conditions. A series of growth steps parallel to (001) face were observed which were attributed to the growth behavior. Moreover, it was found the average chemical composition of the crystal was deviated slightly to the stoichiometric value of PZNT93/7. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献