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991.
Huang M Jin Y Jiang H Sun X Chen H Liu B Wang E Dong S 《The journal of physical chemistry. B》2005,109(32):15264-15271
Multiple-deposited Pt overlayer modified Pt nanoparticle (MD-Pt overlayer/PtNPs) films were deliberately constructed on glassy carbon electrodes through alternately multiple underpotential deposition (UPD) of Ag followed redox replacement reaction by Pt (II) cations. The linear and regular growth of the films characterized by cyclic voltammetry was observed. Atomic force spectroscopy (AFM) provides the surface morphology of the nanostructured Pt films. Rotating disk electrode (RDE) voltammetry and rotating ring-disk electrode (RRDE) voltammetry demonstrate that the MD-Pt overlayer/PtNPs films can catalyze an almost four-electron reduction of O(2) to H(2)O in air-saturated 0.1 M H(2)SO(4). Thus-prepared Pt films behave as novel nanostructured electrocatalysts for dioxygen reduction and hydrogen evolution reaction (HER) with enhanced electrocatalytic activities, in terms of both reduction peak potential and peak current, when compared to that of the bulk polycrystalline Pt electrode. Additionally, it is noted that after multiple replacement cycles, the electrocatalytic activities improved remarkably, although the increased amount of Pt is very low in comparison to that of pre-modified PtNPs due to the intrinsic feature of the UPD-redox replacement technique. In other words, the electrocatalytic activities could be improved markedly without using very much Pt by the technique of tailoring the catalytic surface. These features may provide an interesting way to produce Pt catalysts with a reliable catalytic performance as well as a reduction in cost. 相似文献
992.
993.
SynthesisandCrystalStructureof(Et_4N)_2[Pd_2(mp)_2(mpH)_2]ShiJi-Cheng;HuangXiao-Ying;WenTing-Bin;DengYu-Heng;ChengChang-Neng;Li?.. 相似文献
994.
CrystalStructureandMolecularAbsoluteConfigurationof(+)-Isocedranol(C_(15)H_(26)O)¥LiuJie;ChenMin-Qin(CenterofAnalysis&Measurem... 相似文献
995.
Xiao-pingYan Bao-linHe JieZhang Han-fanLiua 《高分子科学》2005,(4):393-399
Modification of transition metal cations to polymer-stabilized Pt colloidal clusters modified with cinchonidine was studied in enantioselective hydrogenation of methyl pyruvate. Compared to the enantiomeric excess (e.e.) value (71.4%) obtained without the presence of metal cations, obvious e.e. enhancement (up to 82.5%) was resulted from the addition of Zn^2 but with a certain decrease in activity. The reaction parameters in the presence of Zn^2 were also studied. It was found that the Pt colloidal catalysts in the presence of metal cations performed very differently from that in the absence of metal cations. 相似文献
996.
Li Jiang Fushen Lu Qing Chang Yang Liu Huibiao Liu Yuliang Li Wei Xu Guanglei Cui Junpeng Zhuang Xiaofang Li Shu Wang Yinglin Song Daoben Zhu 《Chemphyschem》2005,6(3):481-486
An ultrathin composite film containing anionic Ag-His complexes (His: L-Histidine) and oppositely charged BH-PPV was fabricated by means of the electrostatic layer-by-layer self-assembly technique. UV/Vis spectra showed a continuous deposition process of Ag-His complexes and BH-PPV. The film structure was characterized by using small-angle X-ray diffraction, AFM, and SEM. The nonlinear optical properties of the ultrathin film were studied by using the Z-scan technique with a laser duration of 8 ns at a wavelength of 532 nm. The film sample exhibited a strong nonlinear saturated absorption, with an alpha2 value of -3.9 x 10(-5) mW(-1) and a self-defocusing effect with an n2 value of -4.78 x 10 (-12) m2W(-1). 相似文献
997.
The 1,3-dipolar cycloaddition reaction of meso-tetraaryl porphyrin with 2,6-dichlorobenzonitrile oxide yielded novel isoxazoline-fused chlorins and two stereoisometric bacteriochlorins. The crystal structure of bacteriochlorin was characterized by X-ray diffraction. 相似文献
998.
铜基催化剂的结构、物性及其对混合碳四选择加氢反应的催化性能 总被引:2,自引:0,他引:2
用XRD,XPS,SEM和H2-TPR等手段研究了铜基负载型催化剂的结\r\n构和物性及其对混合碳四加氢脱炔的催化性能.结果表明,在负载铜催\r\n化剂中加入一定量的Co可提高催化剂的加氢脱炔活性,而Co含量较少时\r\n加入少量的Ce也能提高催化剂的活性和选择性.Cu和Co之间存在着相互\r\n协同作用,使得活性组分在催化剂表面偏析,CuO在催化剂表面呈非晶\r\n相分散状态,催化剂颗粒粒径变小,催化剂更容易被还原,从而改善了\r\n催化剂的催化性能. 相似文献
999.
Analysis of acyclovir by high performance capillary electrophoresis with on-column amperometric detection 总被引:1,自引:0,他引:1
The separation of acyclovir (ACV) by high performance capillary electrophoresis (HPCE) with on-column amperometric detection using alpha-amino-5-mercapto-3,4-dithiazole (AMD) as internal standard is described. The calibration line was linear in the range of 0.5-20 mg/L of ACV. The detection limit was 0.15 mg/L of ACV. Its recovery ranged from 98 to 101% with relative standard deviations (RSDs) from 1.9 to 3.2% (n = 5). This method was successfully used for determining ACV in some pharmaceuticals and human urine. Comparable results with HPCE with ultraviolet (UV) detection and amperometric detection were obtained. 相似文献
1000.
Reaction of the semi-rigid ligand 2,4-bis(1-imidazolylmethyl)-mesitylene (m-bimms) with CdCl2 afforded a boat-like molecular rectangle [Cd(m-bimms)Cl2]2 · 1/2H2O (1), with the orientation of the two imidazolyl arms of the ligand in syn-conformation and bridging chloride ions bisecting the macrocycle. Weak Cl· · ·H—C interations further extended the dimers into 1D infinite chains with nanoscopic channels. An analogous reaction with Cd(NO3)2 gave a 1D coordination polymer [Cd(m-bimms)2(NO3)2]n · 2nH2O (2) composed of nanoscopic metallamacrocycles, where the two imidazolyl arms adopt an anti-conformation. Different anions result in different ligand conformations and thus determine the varied molecular architectures. 相似文献