Wang Zeyan, Huang Baibiao, Yu Lin, Dai Ying, Wang Peng, Qin Xiaoyan, Zhang Xiaoyang, Wei Jiyong, Zhan Jie, Jing Xiangyang, Liu Haixia, Whangbo Myung-Hwan
State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, People's Republic of China.
J Am Chem Soc. 2008 Dec 3;130(48):16366-73. doi: 10.1021/ja807030v.
Mn/C-codoped GaN nanostructures were synthesized by carbothermal nitridation with active charcoal as the carbon source. Nanostructures such as zigzag nanowires and nanoscrews were observed by varying the reaction time and the C/Ga molar ratio of the starting material used for the synthesis. The structures and morphologies of the as-grown samples were characterized by X-ray diffraction, scanning electron microscopy, and high-resolution transmission electron microscopy measurements. The doping of both Mn and C in the GaN matrix was confirmed by X-ray photoelectron spectroscopy measurements, and the ferromagnetic properties of Mn/C-codoped GaN samples were confirmed by room-temperature magnetization measurements. The saturation magnetization of Mn/C-codoped GaN increases steadily with increasing C/Ga molar ratio of the starting material at a rate of approximately 0.023 emu/g per C/Ga molar ratio, and the ferromagnetism of Mn/C-codoped GaN can be stronger than that of Mn-doped GaN by a factor of approximately 40. A plausible growth mechanism was proposed, and the role of carbon codoping in tuning the morphology and ferromagnetic property was discussed. Our work suggests that carbon doping in the GaN matrix favors the N sites over the Ga sites, Mn/C-codoping in the GaN matrix is energetically favorable, and the C-codoping strongly enhances the preference of the FM coupling to the AFM coupling between the two doped Mn sites. These suggestions were probed on the basis of first-principles density functional theory electronic structure calculations for a number of model doped structures constructed with a 32-atom 2 x 2 x 2 supercell.
通过以活性炭为碳源的碳热氮化法合成了锰/碳共掺杂的氮化镓纳米结构。通过改变反应时间和合成所用起始材料的碳/镓摩尔比,观察到了锯齿形纳米线和纳米螺旋等纳米结构。通过X射线衍射、扫描电子显微镜和高分辨率透射电子显微镜测量对生长态样品的结构和形貌进行了表征。通过X射线光电子能谱测量证实了锰和碳在氮化镓基体中的掺杂,通过室温磁化测量证实了锰/碳共掺杂氮化镓样品的铁磁性能。锰/碳共掺杂氮化镓的饱和磁化强度随着起始材料碳/镓摩尔比的增加而稳步增加,速率约为每碳/镓摩尔比0.023emu/g,锰/碳共掺杂氮化镓的铁磁性比锰掺杂氮化镓的铁磁性强约40倍。提出了一种合理的生长机制,并讨论了碳共掺杂在调节形貌和铁磁性能方面的作用。我们的工作表明,氮化镓基体中的碳掺杂更倾向于氮位点而非镓位点,氮化镓基体中的锰/碳共掺杂在能量上是有利的,并且碳共掺杂强烈增强了两个掺杂锰位点之间铁磁耦合相对于反铁磁耦合的偏好。基于第一性原理密度泛函理论电子结构计算,对由32个原子的2×2×2超晶胞构建的一些模型掺杂结构进行了探究,得出了这些结论。