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Control of crystallite orientation and size in Fe and FeCo nanoneedles

机译:Fe和FeCo纳米针的微晶取向和尺寸控制

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摘要

Uniform magnetic nanoneedles have been prepared by hydrogen reduction of elongated nanoarchitectures. These precursors are as-prepared or cobalt-coated aggregates of highly oriented haematite nanocrystals (5nm). The final materials are flattened nanoneedles formed by chains of assembled Fe or FeCo single-domain nanocrystals. The microstructural properties of such nanoneedles were tailored using renewed and improved synthetic strategies. In this fashion, the needle elongation and composition, the crystallite size (from 15 up to 30nm), the nanocrystal orientation (with the 110 or 001 directions roughly along the long axis of the nanoneedle) and their type of arrangement (single chains, frustrated double chains and double chains) were controlled by modifying the reduction time, the axial ratio of the precursor haematite and the presence of additional coatings of aluminum or yttrium compounds. The values of the coercivity H _C found for these nanoneedles are compared with the values predicted by the chain of spheres model assuming a symmetric fanning mechanism for magnetization reversal.
机译:已经通过氢还原细长的纳米结构制备了均匀的磁性纳米针。这些前体是高度取向的赤铁矿纳米晶体(5nm)的制备或钴涂层聚集体。最终材料是由组装的Fe或FeCo单畴纳米晶体链形成的扁平纳米针。使用更新和改进的合成策略来定制此类纳米针的微观结构特性。以这种方式,针的伸长率和组成,微晶尺寸(从15到30nm),纳米晶体的取向(大致沿着纳米针的长轴具有110或001方向)及其排列方式(单链受挫)通过改变还原时间,前体赤铁矿的轴向比例以及铝或钇化合物的附加涂层的存在来控制双链和双链)。将这些纳米针的矫顽力H _C的值与球链模型所预测的值进行比较,并假设对称的扇形磁化反转机制。

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