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对名义组份为(Bi_(1-x),M_x)Sr_2YCu_2O_y(x=0.6—0.7)的样品,当M=Cd,Ni和Zn时合成了Bi-1212相材料,实验发现Cd占据Bi位,可以稳定单BiO层,高压氧下退火,在32K出现超导转变,而Zn和Ni进入CuO平面,占据Cu位,破坏了材料的超导电性。用Cd稳定单BiO层还能够合成Bi-1222相化合物,它的固溶范围比Bi-1212大,对这一现像进行了结构上的分析。在不同氧压退火处理下的Bi-1222相样品,电阻随氧压增大而变小,但在4.2K以上未观察到超导转变。
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The title complexes were obtained by the reactions of bis(2,4-pentanedionato)oxovanadium VO(Acac)_2 and m-nitrophenylhydrazide m-NO_2PhCONHNH_2 in the media EtOH and MeOH respectively. The compound (Ⅰ) crystallizes in the space group PT with unit cell dimensions a=8.123(2), b=10.409(5), c=10.822(4), α=65.78(3)°, β=85.50(3)°,γ=89.04(3)°. The compound (Ⅱ) crystallizes in the space group P2_1/a with unit cell dimensions a=7.745(2), b=19.164(5), c=10.787(4), β=107.87(2)°. The resuhs of structural analyses show that the two compounds have the same characteristics: the tridentate ligand formed by condensation occupies three of the four equatorial positions of vanadium and the rest equatorial position is occupied by alkoxy group RO~-. As RO~-group also bridges the sixth coordinated position of each vanadium atom, it brings about the formation of the new type binuclear complexes of vanadium. 相似文献
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ELECTRONIC STRUCTURE OF THE T*-TYPE SUPERCONDUCTORS (Bi0.5Sr1.5)(Y,Ce)2Cu2Oy STUDIED BY PHOTOELECTRON SPECTROSCOPY 下载免费PDF全文
The electronic structure of T*-type compounds (Bi0.5Sr1.5)(Y2-xCex)Cu2Oy has been studied by X-ray photoelectron spectroscopy. From analysis of the results, it was found that cation deficiency in Ce4+ introduced holes to conduction planes in the T* phase as in the p-type infinite layer compounds. Some Cu ions in the sample without cation-deficiency contained two-oxygen coordination, which resulted in the incompleteness of the CuO2 sheets. Bi ions in the T* phase cuprates take exact valence of 3+, Pb ions cannot replace them due to the too large an ionic radius of Pb2+/Pb4+. 相似文献
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用光电子能谱研究了(Bi.Cd)Sr_2(Ln,Ce)_(?)Cu_2O_y的电子结构,以及其与铝之间的反应.芯能级结果表明:(Bi,Cd)Sr_2(Ln,Ce)_(?)Cu_2O_y系列中n=1,2和3三种材料的结果基本一致,并且类似其它超导材料中相同元素的芯能级结果.在(Bi,Cd)Sr_2(Ln,Ce)_(?)Cu_2O_y与铝的界面处,铝与(Bi,Cd)Sr_2(Ln,Ce)_(?)Cu_2O_y中的元素发生强烈反应,Bi—O,Sr—O和Cu—O键受到破坏,铜的价态从+2变为+1,并且同时伴随着超
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常压下Hg系1201相超导铜氧化合物的合成 总被引:1,自引:0,他引:1
本首次报道常压下Hg系1201相超导铜氧化合物的制备,方法简便,制备样品质量较好,超导转变温度达94K。作还进行一步讨论了1201相常压下制备的最佳成相条件及其物相的稳定性。 相似文献
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以二乙酰丙酮氧钒VO(Acac)_2与间硝基苯甲酰肼m-NO_2PhCONHNH_2分别在乙醇和甲醇中反应,得[VO(C_(12)H_(12)N_3O_4)(C_2H_5O)]_2(Ⅰ)和[VO(C_(12)H_(12)N_3O_4)(CH_3O)]_2(Ⅱ)两种晶体。晶体(Ⅰ)属空间群P(?),晶胞参数a=8.123(2),b=10.409(5),c=10.822(4),α=65.78(3)°,β=85.50(3)°,r=89.04(3)°。晶体(Ⅱ)属空间群P2_1/a,a=7.745(2),b=19.164(5),c=10.787(4),β=107.87(2)°。两个晶体均具有共同的结构特征:通过缩合形成的三齿配体占据四个赤道配位位置中的三个,男一个赤道配位位置由醇氧基RO~-所补充而RO~-中的氧原子又兼作桥氧向另一个钒原子的第六位配位,从而导致文献中未报道过的新型双核钒配合物的形成。 相似文献
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ELECTRONIC STRUCTURE OF THE T*-TYPE SUPERCONDUCTORS (Bi0.5Sr1.5)(Y, Ce)2Cu2Oy STUDIED BY PHOTOELECTRON SPECTROSCOPY 下载免费PDF全文
The electronic structure of T*-type compounds (Bi0.5Sr1.5)(Y2-xCex)Cu2Oy has been studied by X-ray photoelectron spectroscopy. From analysis of the results, it was found that cation deficiency in Ce4+ introduced holes to conduction planes in the T* phase as in the p-type infinite layer compounds. Some Cu ions in the sample without cation-deficiency contained two-oxygen coordination, which resulted in the incompleteness of the CuO2 sheets. Bi ions in the T* phase cuprates take exact valence of 3+, Pb ions cannot replace them due to the too large an ionic radius of Pb2+/Pb4+. 相似文献
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SYNTHESIS AT AMBIENT PRESSURE AND SUPERCONDUCTIVITY OF Hg-DOPED TI-BASED DOUBLE [(T1, Hg)-O]-LAYERED CDPHATES 下载免费PDF全文
The Hg-doped T1-based 2201 and 2212 phase layered cuprates have been successfully syn-thesized at ambient pressure and identified by X-ray powder diffraction and electron diffraction analysis. Compared with pure T1-based 2212 phase compound, there are indications that the corresponding Hg-doped T1-based compound (T11.8Hg0.2)Ba2CaCu2Oz exhibits much higher Tc (> 132K). 相似文献