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流动式单电解槽电结晶制[Co/Pt]_n(n≥200)金属多层膜的研究 被引量:4
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作者 曾绍海 印仁和 +2 位作者 曹为民 黄蓉蓉 胡滢 《功能材料》 EI CAS CSCD 北大核心 2004年第4期460-461,共2页
 采用电化学结晶的方法,在硼酸系流动式单电解槽中成功制得[Co/Pt]200多层膜。通过低角度X射线衍射(LXRD)证实了多层膜结构的存在,中角度X射线衍射(MXRD)则证明了Co Pt界面上有CoPt3化合物的存在,首次确认了用电结晶法所得的[Co/Pt]n...  采用电化学结晶的方法,在硼酸系流动式单电解槽中成功制得[Co/Pt]200多层膜。通过低角度X射线衍射(LXRD)证实了多层膜结构的存在,中角度X射线衍射(MXRD)则证明了Co Pt界面上有CoPt3化合物的存在,首次确认了用电结晶法所得的[Co/Pt]n多层膜中存在CoPt3化合物的事实。 展开更多
关键词 电化学结晶 流动式单电解檀 多层膜 X射线衍射
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(BEDT-TTF)_2HgCl_3·CHCl_2CH_2Cl晶体的合成与结构
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作者 刘陟 于文涛 +6 位作者 方奇 刘志强 王筱梅 任燕 延云兴 于晓强 蒋民华 《人工晶体学报》 EI CAS CSCD 北大核心 2000年第S1期42-,共1页
双亚乙基二硫四硫富瓦烯 (简称BEDT TTF)的盐具有非同寻常的电荷转移性质及超导电性 ,近年来引起人们的浓厚兴趣。我们采用电化学结晶的方法 ,在恒电流I=1 μA的条件下 ,制备了几种BEDT TTF的阳离子盐 ,其中一种新晶体是 (BEDT TTF) 2 H... 双亚乙基二硫四硫富瓦烯 (简称BEDT TTF)的盐具有非同寻常的电荷转移性质及超导电性 ,近年来引起人们的浓厚兴趣。我们采用电化学结晶的方法 ,在恒电流I=1 μA的条件下 ,制备了几种BEDT TTF的阳离子盐 ,其中一种新晶体是 (BEDT TTF) 2 HgCl3 ·CHCl2 CH2 Cl,晶体是以 1 ,1 ,2 三氯乙烷和乙醇 (体积比 9∶1 )的混合溶液作溶剂 ,电解一个月得到的 ,获得的晶体的最大尺寸为 4mm× 3mm×0 .0 8mm。利用‘BrukerP4’单晶衍射仪 ,测定其单晶结构 ,结构参数如下 :化学式 (C10 H8S8) 2 HgCl3 ·CHCl2 CH2 Cl,Mr =1 2 0 9.6 2 ,单斜晶系 ,C2空间群 ,a =3.92 36 ( 5 )nm ,b =0 .6 6 76 0 ( 1 4)nm ,c =1 .4881 ( 3)nm ,β =95 .5 8( 2 )° ,V =3.8794( 1 2 )nm3 ,Z =4,Dx=2 .0 71Mg/M3 ,λ(MoKα) =0 .0 71 0 73nm ,F( 0 0 0 ) =2 35 6 ,T =2 93( 2 )K ,R =0 .0 6 88对 5 799可观测的衍射点。单晶结构显示BEDT TTF分子沿c轴方向形成堆积 ,沿a轴方向肩并肩排列 ,并且BEDT TTF分子堆积沿此方向被HgCl-3 和 1 ,1 ,2 三氯乙烷层分割开。有关导电和磁学性能研究正在进一步进行之中。 展开更多
关键词 有机盐晶体 电化学结晶 晶体结构
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Influence of surface treatment of carbon fiberson electrochemical crystallization of calcium phosphate 被引量:1
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作者 陶可 黄苏萍 周科朝 《Journal of Central South University of Technology》 2005年第2期113-116,共4页
Electrodeposition technique was used to coat calcium phosphate on carbon fiber which can be used to reinforce hydroxyapatite. The differences between fibers treated with and without nitric acid in electrodeposition we... Electrodeposition technique was used to coat calcium phosphate on carbon fiber which can be used to reinforce hydroxyapatite. The differences between fibers treated with and without nitric acid in electrodeposition were evaluated. The X-ray diffractometry results show that CaHPO4·2H2O is obtained as the kind of calcium phosphate coating on carbon fiber. The scanning electron microscopy photographs and deposit kinetic curve indicate that the influences of the functional group attained by nitric acid treatment, the crystal morphology and crystallization of the coating layers on the fiber with and without treatment rate are obviously different. The functional group, especially the acidic group, can act as nucleation centers of electrochemical crystallization. 展开更多
关键词 ELECTRODEPOSITION dicalcium phosphate dihydrate carbon fiber surface treatment
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Influences of substituting Ni with M(M=Cu,Co,Mn)on gaseous and electrochemical hydrogen storage kinetics of Mg_(20)Ni_(10) alloys 被引量:3
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作者 张羊换 杨泰 +3 位作者 翟亭亭 尚宏伟 张国芳 赵栋梁 《Journal of Central South University》 SCIE EI CAS 2014年第5期1705-1713,共9页
In this work,a comprehensive comparison regarding the impacts of M(M=Cu,Co,Mn)substitution for Ni on the structures and the hydrogen storage kinetics of the nanocrystalline and amorphous Mg20Ni10-xMx(M=Cu,Co,Mn; x=0-4... In this work,a comprehensive comparison regarding the impacts of M(M=Cu,Co,Mn)substitution for Ni on the structures and the hydrogen storage kinetics of the nanocrystalline and amorphous Mg20Ni10-xMx(M=Cu,Co,Mn; x=0-4)alloys prepared by melt spinning has been carried out.The analysis of XRD and TEM reveals that the as-spun(M=None,Cu)alloys display an entire nanocrystalline structure,whereas the as-spun(M=Co,Mn)alloys hold a mixed structure of nanocrystalline and amorphous structure when M content x=4,indicating that the substitution of M(M=Co,Mn)for Ni facilitates the glass formation in the Mg2Ni-type alloy.Besides,all the as-spun alloys have a major phase of Mg2Ni but M(M=Co,Mn)substitution brings on the formation of some secondary phases,MgCo2 and Mg phases for M=Co as well as MnNi and Mg phases for M=Mn.Based upon the measurements of the automatic Sieverts apparatus and the automatic galvanostatic system,the impacts engendered by M(M=Cu,Co,Mn)substitution on the gaseous and electrochemical hydrogen storage kinetics of the alloys appear to be evident.The gaseous hydriding kinetics of the alloys first rises and then declines with the growing of M(M=Cu,Co,Mn)content.Particularly,the M(M= Mn)substitution results in a sharp drop in the hydriding kinetics when x=4.The M(M=Cu,Co,Mn)substitution ameliorates the dehydriding kinetics dramatically in the order(M=Co)>(M=Mn)>(M=Cu).The electrochemical kinetics of the alloys visibly grows with M content rising for(M=Cu,Co),while it first increases and then declines for(M=Mn). 展开更多
关键词 Mg2Ni-type alloy element substitution nanocrystalline and amorphous hydrogen storage kinetics
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