Abstract The (Fe x Co 1−x ) 3 B (x = 0.0, 0.1, 0.2, 0.3) compounds have been prepared by induction melting with subsequent annealing. All of the compounds form in the orthorhombic Fe 3 C-type structure and exhibit ferromagnetic behaviour: the Curie temperature increases from 750 K for x = 0.0 to 923 K for x = 0.3. Magnetic domain images obtained by Kerr microscopy reveal the presence of uniaxial magnetocrystalline
摘要 (Fe x Co 1-x ) 3 B (x = 0.0, 0.1, 0.2, 0.3) 化合物已通过感应熔炼和随后的退火制备。所有化合物均以正交 Fe 3 C 型结构形式形成并表现出铁磁行为:居里温度从 x = 0.0 时的 750 K 增加到 x = 0.3 时的 923 K。通过克尔显微镜获得的磁畴图像揭示了单轴磁晶各向异性的存在。已确定磁取向细粒的磁晶各向异性能量和各向异性场。Co 3 B (x = 0.0) 获得了651 kJm -3 的各向异性能量,发现各向异性能量随着Fe含量的增加而降低,x = 0.3时达到507 kJm -3 的值。
Efficient photocatalytic CO<sub>2</sub> reduction mediated by transitional metal borides: metal site-dependent activity and selectivity
The Oxygen evolution reaction on cobalt borides and composite cobalt borides was investigated in a 6M KOH solution (1 M=1 mol dm−3) using the factor of the magnetic properties. In the system of cobalt borides (Co:B=3:1) prepared at various sintering temperatures, the boride having a higher saturation magnetization revealed a higher activity of the oxygen evolution reaction. In the system of composite cobalt borides which have various magnetic moments, μB, a clear correlation between the activity of the oxygen evolution reaction and the saturation magnetization (or magnetic moment, μB) was observed for several composite cobalt boride species (i.e., Co–Fe–B, Co–Ni–B, Co–Mn–B, and Co–B). Among the composite cobalt boride species, the cobalt iron boride (Co:Fe:B=1:2:1) sintered at 450 °C showed the highest activity of oxygen evolution reaction in a 6 M KOH solution. The conditions of oxide formation on Co–Fe–B(1:2:1) and on Co–B(3:1) in a 6 M KOH solution were compared with those on cobalt by means of voltammetry and chronopotentiometry. It was concluded that the ease and stability of oxide films in higher oxidation states are strongly correlated to the activity of the oxygen evolution reaction which occurs on more highly oxidized oxide films.
在6M KOH溶液(1 M=1 mol dm−3)中,利用磁性质因子研究了钴硼化物和复合钴硼化物中的氧析出反应。在各种烧结温度下制备的钴硼化物(Co:B=3:1)体系中,具有更高饱和磁化的硼化物显示出更高的氧析出反应活性。在具有不同磁矩μB的复合钴硼化物体系中,观察到几种复合钴硼化物(即Co–Fe–B、Co–Ni–B、Co–Mn–B和Co–B)的氧析出反应活性与饱和磁化强度(或磁矩μB)之间存在明显的相关性。在复合钴硼化物中,在450 °C下烧结的钴铁硼化物(Co:Fe:B=1:2:1)在6 M KOH溶液中显示出最高的氧析出反应活性。通过伏安法和恒电位法,将6 M KOH溶液中Co–Fe–B(1:2:1)和Co–B(3:1)的氧化物形成条件与钴的氧化物形成条件进行了比较。结果表明,高氧化态下氧化物膜的易形成性和稳定性与氧析出反应
Two Borides with the Cementite Structure
作者:STIG RUNDQVIST
DOI:10.1038/181259a0
日期:1958.1
AN investigation by X-ray powder methods of the nickelâboron and the cobaltâboron systems has revealed the existence of two isomorphous borides, Ni3B and Co3B. A nickel boride with a boron content about 25 atom per cent has previously been reported by Andersson and Kiessling1, but no reports on Co3B seem to have been published.
Photoemission and electronic structure of crystalline Co3B and amorphous Co - P - B
作者:A. Amamou、G. Krill
DOI:10.1016/0038-1098(79)90011-5
日期:1979.9
Abstract We present an XPS and UPS study of crystallineCo, Co 3 B and Co 78 P 14 B 8 glassy metal. For Co 3 B the electronic distribution curves (EDC) of the valence band and the previous specific heat and magnetic results are interpreted in a qualitative model where : i) the s-p cobalt-boron bonding states lie in the low part of the band, the upper levels being mainly cobalt d states and ii) a large
摘要 我们介绍了晶体 Co、Co 3 B 和 Co 78 P 14 B 8 玻璃态金属的 XPS 和 UPS 研究。对于 Co 3 B,价带的电子分布曲线 (EDC) 和先前的比热和磁结果在定性模型中解释,其中: i) sp 钴-硼键合状态位于带的低部,上能级主要是钴 d 态和 ii) 大部分自旋带的大密度态存在于费米能级。对于非晶 Co 78 P 14 B 8 ,EDC 显示 EF 位于高态密度区域,建议磷 p 态 ae 集中在 7.5 eV。光电发射和磁性结果也可以在先前模型的框架中进行解释。