论文标题

部分可观测时空混沌系统的无模型预测

Unusual phase formation in reactively sputtered La-Co-O perovskite thin films

论文作者

Piotrowiak, Tobias H., Zehl, Rico, Suhr, Ellen, Banko, Lars, Kohnen, Benedikt, Rogalla, Detlef, Ludwig, Alfred

论文摘要

基于LA的钙钛矿是一种多功能的材料类别,可用于固体氧化物燃料电池和电催化水分裂。在制造成分的过程中,观察到了一种不寻常的催化材料的基于LA-CO的氧化物系统的材料库,观察到了一种异常的相形形成现象:代替了预期的连续成分梯度,而是具有同质组成和单相结构(LA2O3或stoichieChiotion La-perovskite la-perovskite)的区域。这种现象发生在反应性共同分解过程中,并取决于O2-Flux和底物温度,该温度从室温至700 c进行了研究,并且与使用的底物无关。它可以描述为一种自组织的生长,在该生长中,过量的过渡金属不能纳入生长的膜和形成的单相区域。假设,由于LA和LA2O3和La-Perovskites的高反应性以及显着较低的形成能,基于LA的氧化物膜的反应性溅射可以转变为膜的生长,变成部分CVD样过程,从而导致单相区域的异常自组织生长。可以利用这种现象来探索多毛钙钛矿薄膜库,其中La-perovskites的B点原子是系统地取代的。

La-based perovskites are a versatile class of materials that are of interest for solid oxide fuel cells and electrocatalytic water splitting. During fabrication of composition spread materials libraries of La-Co-based oxide systems for the discovery of new catalytic materials, an unusual phase formation phenomenon was observed: instead of the expected continuous composition gradient, regions with homogeneous composition and single-phase structure (La2O3 or stoichiometric La-perovskite) form. This phenomenon occurs during reactive co-sputtering and is dependent on O2-flux and substrate temperature, investigated from room temperature up to 700 C and is independent of the used substrate. It can be described as a self-organized growth, where excess transition metal cannot be incorporated into the growing film and the forming single-phase regions. It is hypothesized that due to the high reactivity of La and the significantly low formation energies of La2O3 and La-perovskites, the reactive sputter deposition of La-based oxide films can turn, regarding film growth, into a partial CVD-like process which results in the unusual self-organized growth of single-phase regions. This phenomenon can be leveraged for the exploration of multinary perovskite thin film libraries, where the B-site atoms of La-perovskites are systematically substituted.

扫码加入交流群

加入微信交流群

微信交流群二维码

扫码加入学术交流群,获取更多资源