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Design, synthesis characterization of precursors for chemical vapor deposition of oxide-based electronic materials

机译:基于氧化物电子材料的化学气相沉积前体的设计,合成表征

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Ferroelectric and other high dielectric constant metal oxides currently are sought-after for a variety of applications in the electronics industry. To meet the demand of preparation of these interesting materials in a manner compatible with traditional silicon-based fabrication procedures, chemical vapor deposition routes are desired for film growth. Compounds displaying high vapor phase stability are necessary as precursors for these applications. Additionally, in general, it is preferred to utilize compounds in a liquid state, due to the more rapid re-establishment of equilibrium at a liquid-vapor interface, compared to that present at a solid-vapor interface. This combination of desired molecular properties, in turn, presents a great challenge to the coordination chemist. Several of the metals of interest for these uses reside in groups 2-5. Common design features are emerging for the ligands best suited for attachment to these metals for subsequent utilization in the deposition of metal oxides. In order to achieve coordinative saturation of the relatively high ionic radii exhibited by most of these elements, multidentate, monoanionic ligands are relied upon. In the past, most often, homoleptic ligand sets have been employed, thereby reducing the chance for ligand scrambling to occur during the growth process. Such disproportionation processes have been credited, in previous work, with the observation of a temporal decay in vapor pressure of heteroleptic compounds. In some interesting new developments, it has been found that heteroleptic compounds possess sufficient vapor phase integrity to permit their evaluation as CVD precursors. These, and related, results are presented herein.
机译:目前在电子工业中寻求铁电和其他高介电常数金属氧化物。为了满足以与传统的基于硅制造程序相容的方式制备这些有趣材料的需求,需要化学气相沉积途径对薄膜生长。显示高气相稳定性的化合物是这些应用的前体必需的。另外,通常优选利用液态的化合物,其由于在固体 - 蒸汽界面处存在于液体蒸汽界面处的平衡越快地建立平衡。反过来,这种所需分子特性的这种组合对协调化学家呈现出巨大挑战。这些使用的几金金属均为2-5组。对于最适合于附着于这些金属的配体,常见的设计特征是为了随后利用金属氧化物的沉积而产生的。为了实现大多数这些元素呈现的相对高离子半径的协调饱和,依赖于多型单甘蔗酸酯配体。在过去,最常见的是,已经采用了经络配体组,从而减少了在生长过程中发生配体争吵的机会。在以前的工作中,这种歧化过程已经归功于观察异常衰减的异料化合物的蒸气压。在一些有趣的新发展中,已经发现异常化合物具有足够的气相完整性,以允许将其评价为CVD前体。这些和相关的结果在此提出。

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