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Manipulating coupling state and magnetism of Mn-doped ZnO nanocrystals by changing the coordination environment of Mn via hydrogen annealing

机译:通过氢退火改变Mn的配位环境来控制Mn掺杂ZnO纳米晶的耦合态和磁性

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摘要

Mn-doped ZnO nanocrystals are synthesized by a wet chemical route and treated in H2/Ar atmosphere with different H2/Ar ratios. It is found that hydrogen annealing could change the coordination environment of Mn in ZnO lattice and manipulate the magnetic properties of Mn-doped ZnO. Mn ions initially enter into interstitial sites and a Mn3+O6 octahedral coordination is produced in the prepared Mn-doped ZnO sample, in which the nearest neighbor Mn3+ and O2 ions could form a Mn3+-O2--Mn3+ complex. After H2 annealing, interstitial Mn ions can substitute for Zn to generate the Mn2+O4 tetrahedral coordination in the nanocrystals, in which neighboring Mn2+ ions and H atoms could form a Mn2+-O2--Mn2+ complex and Mn-H-Mn bridge structure. The magnetic measurement of the as-prepared sample shows room temperature paramagnetic behavior due to the Mn3+-O2--Mn3+ complex, while the annealed samples exhibit their ferromagnetism, which originates from the Mn-H-Mn bridge structure and the Mn-Mn exchange interaction in the Mn2+-O2--Mn2+ complex.
机译:Mn掺杂的ZnO纳米晶体是通过湿化学方法合成的,并在H2 / Ar气氛中以不同的H2 / Ar比进行处理。发现氢退火可以改变ZnO晶格中Mn的配位环境,并控制Mn掺杂的ZnO的磁性。 Mn离子最初进入间隙位,在制备的Mn掺杂ZnO样品中产生Mn3 + O6八面体配位,其中最邻近的Mn3 +和O2离子可形成Mn3 + -O2--Mn3 +络合物。经过H2退火后,间隙中的Mn离子可以代替Zn在纳米晶体中生成Mn2 + O4四面体配位,其中相邻的Mn2 +离子和H原子可以形成Mn2 + -O2--Mn2 +配合物和Mn-H-Mn桥结构。所制备样品的磁性测量结果显示,由于Mn3 + -O2--Mn3 +络合物,室温下的顺磁行为,而退火后的样品则表现出其铁磁性,这是由Mn-H-Mn桥结构和Mn-Mn交换引起的Mn2 + -O2--Mn2 +配合物中的相互作用。

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