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首页> 外文期刊>Nanoscale >Bulk and surface exsolution produces a variety of Fe-rich and Fe-depleted ellipsoidal nanostructures in La0.6Sr0.4FeO3 thin films
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Bulk and surface exsolution produces a variety of Fe-rich and Fe-depleted ellipsoidal nanostructures in La0.6Sr0.4FeO3 thin films

机译:体积和表面脱溶产生各种各样的Fe-rich和Fe-depleted椭圆形在La0.6Sr0.4FeO3纳米结构薄膜

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The past several years have seen a resurgence in the popularity of metal exsolution as an approach to synthesize advanced materials proposed for novel catalytic, magnetic, optical, and electrochemical properties. Whereas most studies to-date have focused on surface exsolution (motivated by catalysis), we instead report on the diversity of nanostructures formed in La0.6Sr0.4FeO3 thin films during sub-surface or so-called ‘bulk’ exsolution, in addition to surface exsolution. Bulk exsolution is a promising approach to tuning the functionality of materials, yet there is little understanding of the nanostructures exsolved within the bulk and how they compare to those exsolved at gas–solid interfaces. This work combines atomic- and nano-scale imaging and spectroscopy techniques applied using a state-of-the-art aberration-corrected scanning transmission electron microscope (STEM). In doing so, we present a detailed atomic-resolution study of a range of Fe-rich and Fe-depleted nanostructures possible via exsolution, along with qualitative and quantitative chemical analysis of the exsolved nanostructures and oxide phases formed throughout the film. Local structural changes in the perovskite matrix, coinciding with nanostructure exsolution, are also characterized with atomic-resolution STEM imaging. Fe exsolution is shown to create local A-site rich domains of Ruddlesden–Popper phase, and some stages of this phase formation have been demonstrated in this work. In particular, phase boundaries are found to be the primary nucleation sites for bulk and surface exsolution, and the exsolved particles observed here tend to be ellipsoidal with shape factor of 1.4. We report a range of nanostructure types (core–shell, bulk core–shell, adjacent, and independent particles), revealing several possible avenues of future exploration aimed to understand the formation mechanism of each exsolution type and to develop their functionality. This work is thus relevant to materials scientists and engineers motivated to understand and utilize exsolution to synthesize materials with predictable nanostructures.
机译:过去几年中复苏金属脱溶的流行方法提出了合成先进的材料新颖的催化、磁性、光学和电化学性质。她们都集中在表面脱溶(出于催化),我们报告纳米结构形成的多样性在地下或La0.6Sr0.4FeO3薄膜所谓的“散装”脱溶,除了表面脱溶。有前途的方法来调优的功能材料,但几乎没有理解内的纳米结构exsolved散装如何比较那些在气固exsolved吗接口。纳米成像技术和光谱技术应用使用最先进的aberration-corrected扫描透射电子显微镜(杆)。提供一个详细的原子水平的研究Fe-rich和Fe-depleted纳米结构可能通过脱溶和定性和定量化学分析exsolved纳米结构和氧化阶段形成的整个电影。钙钛矿矩阵,与纳米结构的出溶作用,也为特征与原子水平抑制成像。脱溶显示创建本地网站丰富域的Ruddlesden-Popper阶段,和一些这一阶段形成的阶段在这项工作。边界发现初级成核网站的体积和表面脱溶,exsolved粒子倾向于观察到这里椭球形状系数为1.4。各种纳米结构类型(核壳、散装核壳、毗邻和独立的粒子),揭示未来的几种可能途径探索旨在理解形成每个出溶作用类型和发展的机制它们的功能。材料科学家和工程师动机理解和利用脱溶合成材料和可预测的nanostructures。

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