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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >First-Principles Bottom-Up Study of 1D to 3D Magnetic Transformation in the Copper Pyrazine Dinitrate S = 1/2 Antiferromagnetic Crystal
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First-Principles Bottom-Up Study of 1D to 3D Magnetic Transformation in the Copper Pyrazine Dinitrate S = 1/2 Antiferromagnetic Crystal

机译:吡嗪铜S = 1/2反铁磁晶体中1D到3D磁转换的第一性原理自下而上的研究

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On the basis of magnetic susceptibility and heat capacity data, copper pyrazine dinitrate crystal [abbreviated CuPz(NO3)2] has long been considered a good prototype for S = 1/2 antiferromagnetic (AFM) Heisenberg chain behavior down to 0.05 K. However, a recent muon-spin rotation experiment indicated the presence of a previously unnoticed 1D to 3D magnetic transition below 0.107 K. Our aim in this work is to perform a rigorous quantitative study of the mechanism of this 1D-3D magnetic transformation, by doing a first-principles bottom-up study of the CuPz(NO3)2 crystal at 158 K, where the magnetic properties are clearly 1D, and at 2 K, at which the neutron structure (reported in this work) is considered nearly identical with that below 0.1 K (due to small thermal effects). A change in the magnetic topology is found between these two structures: at 158 K, there are isolated AFM spin chains (Jintra = -5.23 cm-1),while at 2 K, the magnetic chains (Jintra = -5.96 cm-1) weakly interact (the largest of the Jinter parameters is -0.09 cm-1). This change is caused by thermal contraction upon cooling (no crystallographic phase transition is detected down to 2 K, and one will not likely occur below that temperature). The computed and experimental magnetic susceptibility χ(T) curves are nearly identical. The calculated heat capacity Cp(T) curve has a maximum at 6.92 K, close to the 5.20 K maximum found in the experimental curve at zero external field. In spite of the 3D magnetic topology of the crystal at low temperature, the magnetic susceptibility and heat capacity curves behave as a pure 1D AFM chain in all regions because of the large Jintra/Jinter ratio (66.2 in absolute value) and the effect of including the Jinter interactions will not be easily appreciated in any of these experiments. The impact of the presence of odd- and evenmembered regular AFM finite chains in the CuPz(NO3)2 crystal has also been evaluated. Odd-membered interacting chains produce an increase in both χ(T) and Cp(T) curves when the temperature is very close to zero, in agreement with the experimental observations, while even-membered chains produce a small shoulder in the Cp(T) curve between 0.8 and 5 K. No changes are seen in the remaining regions. Concerning the spin gap, odd-membered chains present a quasi-zero gap but the finite even-membered chains still have a sizable one. Finally, the effect of increasing the magnitude of Jinter was investigated by fixing the value of Jintra to that found for the 2 K CuPz(NO3)2 crystal. The magnetic susceptibility and heat capacity curves remain practically unchanged.
机译:根据磁化率和热容数据,长期以来人们一直认为重氮化吡嗪铜酸铜晶体[缩写为CuPz(NO3)2]是S = 1/2反铁磁(AFM)Heisenberg链行为(低至0.05 K)的良好原型。最近的muon-spin旋转实验表明,存在低于0.107 K的先前未被察觉的1D到3D磁跃迁。我们的工作目标是通过首先进行1D-3D磁跃迁的机理进行严格的定量研究。原理对CuPz(NO3)2晶体在158 K时的自下而上的研究,该处的磁性明显为一维,而在2 K时,认为中子结构(在这项工作中报道)与在0.1 K以下的中子结构几乎相同K(由于较小的热效应)。在这两个结构之间发现了磁拓扑的变化:在158 K处,存在孤立的AFM自旋链(金特拉= -5.23 cm-1),而在2 K时,磁链(Jintra = -5.96 cm-1)弱交互(Jinter参数的最大值为-0.09 cm-1)。这种变化是由冷却时的热收缩引起的(在低至2 K时未检测到结晶相变,在该温度以下不太可能发生结晶相变)。计算和实验的磁化率χ(T)曲线几乎相同。计算出的热容量Cp(T)曲线的最大值为6.92 K,接近于在零外部电场下在实验曲线中找到的最大值5.20K。尽管晶体在低温下具有3D磁性拓扑,但由于较大的Jintra / Jinter比(绝对值为66.2),并且磁化率和热容曲线在所有区域均表现为纯1D AFM链,因此其影响在任何这些实验中,Jinter交互都不容易理解。还评估了CuPz(NO3)2晶体中奇数和偶数规则AFM有限链的存在的影响。当温度非常接近于零时,奇数相互作用的链会同时增加χ(T)和Cp(T)曲线,这与实验观察结果一致,而奇数相互作用的链在Cp(T )曲线在0.8至5 K之间。其余区域则看不到任何变化。关于自旋间隙,奇数元链呈现准零间隙,而有限的偶数链仍具有相当大的间隙。最后,通过将Jintra的值固定为2 K CuPz(NO3)2晶体的值,研究了提高Jinter幅度的效果。磁化率和热容曲线实际上保持不变。

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