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作 者:徐静[1,2] 齐伟华[1] 纪登辉[1,3] 李壮志[1] 唐贵德[1] 张晓云 尚志丰 朗莉莉
机构地区:[1]河北省新型薄膜材料实验室,河北师范大学物理科学与信息工程学院,石家庄050024 [2]河北工程大学理学院,邯郸056038 [3]六盘水师范学院物理与电子科学系,六盘水553004
出 处:《物理学报》2015年第1期309-319,共11页Acta Physica Sinica
基 金:国家自然科学基金(批准号:11174069);河北省教育厅青年基金(批准号:QN20131008)资助的课题~~
摘 要:采用固相反应法制备了系列样品TixNi1-xFe2O4(x=0.0,0.1,0.2,0.3,0.4).室温下的X射线衍射谱表明样品全部为(A)[B]2O4型单相立方尖晶石结构,属于空间群Fdˉ3m.样品的晶格常数随Ti掺杂量的增加而增大.样品在10 K温度下的比饱和磁化强度σS随着Ti掺杂量x的增加逐渐减小.研究发现,当Ti掺杂量x 0.2时,磁化强度σ随温度T的变化曲线出现两个转变温度TL和TN.当温度低于TN时,磁化强度明显减小;当温度达到TL时,dσ/d T具有最大值.σ-T曲线的这些特征表明,由于Ti掺杂在样品中出现了附加的反铁磁结构.这说明样品中的Ti离子不是无磁性的+4价离子,而是以+2和+3价态存在,其离子磁矩的方向与Fe和Ni离子的磁矩方向相反.利用本课题组提出的量子力学方势垒模型拟合样品在10 K温度下的磁矩,得到了Ti,Fe和Ni三种阳离子在(A)位和[B]位的分布情况,并发现在所有掺杂样品中,80%的Ti离子以+2价态占据尖晶石结构的[B]位.Spinel ferrite samples TixNi1?xFe2O4(x=0.0,0.1,0.2,0.3,0.4) were prepared using conventional solid reaction method. The sample exhibit a single-phase cubic spinel structure with a space group obtained Fd3m. The lattice parameter a increases with the increase of Ti doping level x. But the specific saturation magnetizations, as, gradually decrease with increasing Ti doping level x at 10 K and 300 K. It is interesting that when the doping level x ≥0.2, two transition temperatures, TL and TN, are found: when the temperature is lower than TN, the magnetization is obviously decreased, while at the temperature TL, dσ/dT reaches a maximum value. This phenomenon indicates that an additional antiferromagnetic structure arises in the traditional spinel phase of ferrites which results from Ti doping, that Ti ions will show the form of Ti3+ and Ti2+ cations which have magnetic moments, and that the magnetic moments of the Ti cations are opposite to those of the Fe and Ni cations. The dependence of the magnetic moments of the samples on the Ti doping level x at 10 K was fitted successfully using the quantum-mechanical potential barrier model proposed earlier by our group. In the fitting process, the distributions of Ti, Ni and Fe cations in the samples are obtained. It is found that 80% of the Ti cations will occupy the [B] sites in Ti2+ form.
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