Norberg Nick S, Kittilstved Kevin R, Amonette James E, Kukkadapu Ravi K, Schwartz Dana A, Gamelin Daniel R
Department of Chemistry, University of Washington, Seattle, Washington 98195-1700, USA.
J Am Chem Soc. 2004 Aug 4;126(30):9387-98. doi: 10.1021/ja048427j.
We report the synthesis of colloidal Mn(2+)-doped ZnO (Mn(2+):ZnO) quantum dots and the preparation of room-temperature ferromagnetic nanocrystalline thin films. Mn(2+):ZnO nanocrystals were prepared by a hydrolysis and condensation reaction in DMSO under atmospheric conditions. Synthesis was monitored by electronic absorption and electron paramagnetic resonance (EPR) spectroscopies. Zn(OAc)(2) was found to strongly inhibit oxidation of Mn(2+) by O(2), allowing the synthesis of Mn(2+):ZnO to be performed aerobically. Mn(2+) ions were removed from the surfaces of as-prepared nanocrystals using dodecylamine to yield high-quality internally doped Mn(2+):ZnO colloids of nearly spherical shape and uniform diameter (6.1 +/- 0.7 nm). Simulations of the highly resolved X- and Q-band nanocrystal EPR spectra, combined with quantitative analysis of magnetic susceptibilities, confirmed that the manganese is substitutionally incorporated into the ZnO nanocrystals as Mn(2+) with very homogeneous speciation, differing from bulk Mn(2+):ZnO only in the magnitude of D-strain. Robust ferromagnetism was observed in spin-coated thin films of the nanocrystals, with 300 K saturation moments as large as 1.35 micro(B)/Mn(2+) and T(C) > 350 K. A distinct ferromagnetic resonance signal was observed in the EPR spectra of the ferromagnetic films. The occurrence of ferromagnetism in Mn(2+):ZnO and its dependence on synthetic variables are discussed in the context of these and previous theoretical and experimental results.
我们报道了胶体锰(II)掺杂氧化锌(Mn(2+):ZnO)量子点的合成以及室温铁磁纳米晶薄膜的制备。Mn(2+):ZnO纳米晶体是在大气条件下于二甲基亚砜中通过水解和缩合反应制备的。通过电子吸收光谱和电子顺磁共振(EPR)光谱监测合成过程。发现醋酸锌(Zn(OAc)(2))能强烈抑制O(2)对Mn(2+)的氧化,从而使Mn(2+):ZnO的合成可在有氧条件下进行。使用十二烷基胺从制备好的纳米晶体表面去除Mn(2+)离子,以得到高质量的内部掺杂Mn(2+):ZnO胶体,其形状接近球形且直径均匀(6.1 +/- 0.7 nm)。对高分辨率X波段和Q波段纳米晶体EPR光谱的模拟,结合磁化率的定量分析,证实锰以Mn(2+)的形式替代掺入ZnO纳米晶体中,其形态非常均匀,与块状Mn(2+):ZnO的区别仅在于D应变的大小。在纳米晶体的旋涂薄膜中观察到了强铁磁性,300 K时的饱和磁矩高达1.35 μB/Mn(2+),居里温度T(C) > 350 K。在铁磁薄膜的EPR光谱中观察到了明显的铁磁共振信号。结合这些以及之前的理论和实验结果,讨论了Mn(2+):ZnO中铁磁性的出现及其对合成变量的依赖性。