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首页> 外文期刊>Physical chemistry chemical physics: PCCP >Low energy electron-induced decomposition of (eta(5)-Cp)Fe(CO)(2)Mn(CO)(5), a potential bimetallic precursor for focused electron beam induced deposition of alloy structures
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Low energy electron-induced decomposition of (eta(5)-Cp)Fe(CO)(2)Mn(CO)(5), a potential bimetallic precursor for focused electron beam induced deposition of alloy structures

机译:低能量电子诱导的(ETA(5)-CP)Fe(CO)(2)Mn(Co)(Co)(5)的分解,聚焦电子束诱导合金结构的潜在双金属前体

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摘要

The production of alloyed nanostructures presents a unique problem in focused electron beam induced deposition (FEBID). Deposition of such structures has historically involved the mixing of two or more precursor gases in situ or via multiple channel gas injection systems, thereby making the production of precise, reproducible alloy compositions difficult. Promising recent efforts to address this problem have involved the use of multi-centred, heterometallic FEBID precursor species. In this vein, we present here a study of low-energy electron interactions with cyclopentadienyl iron dicarbonyl manganese pentacarbonyl ((eta(5)-Cp)Fe(CO)(2)Mn(CO)(5)), a bimetallic species with a polyhapto ligand (Cp) and seven terminal carbonyl ligands. Gas phase studies and coupled cluster calculations of observed low-energy electron-induced reactions were conducted in order to predict the performance of this precursor in FEBID. In dissociative electron attachment, we find single CO loss and cleavage of the Fe-Mn bond, leading to the formation of [Mn(CO)(5)](-), to be the two dominant channels. Contributions through further CO loss from the intact core and the formation of [Mn(CO)(4)](-) are minor channels. In dissociative ionization (DI), the fragmentation is significantly more extensive and the DI spectra are dominated by fragments formed through the loss of 5 and 6 CO ligands, and fragments formed through cleavage of the Fe-Mn bond accompanied by substantial CO loss. The gas phase fragmentation channels observed are discussed in relation to the underlying processes and their energetics, and in context to related surface studies and the likely performance of this precursor in FEBID.
机译:合金纳米结构的生产在聚焦电子束诱导沉积(Febid)中具有独特的问题。这种结构的沉积历史上涉及原位或通过多通道气体喷射系统的两种或更多种前体气体的混合,从而使得生产精确,可再现的合金组合物难以。有希望解决这一问题的努力涉及使用多居中,异常的Febid前体物种。在该静脉中,我们在此提出了一种与环戊二烯基铁二羰基二羰基苯基的低能量电子相互作用(((5)-CP)Fe(CO)(2)Mn(Co)(5)),一种双金属物种多耐托乙酰乙烷配体(CP)和7末端羰基配体。进行了观察到的低能量电子诱导反应的气相研究和耦合簇计算,以预测Febid的这种前体的性能。在解离电子附件中,我们发现Fe-Mn键的单一CO损耗和切割,导致形成[Mn(CO)(5)]( - ),是两个主导通道。通过完整的核心进一步丧失和[Mn(CO)(4)]( - )的贡献是次要通道的贡献。在离灭电离(DI)中,碎片显着更广泛,DI光谱由通过5和6 Co配体的损失形成的片段来支配,并且通过伴随Fe-Mn键形成的片段伴随着实质性的Co损失。观察到的气相碎片通道是关于潜在的过程及其能量学,以及在仅特2例中的相关表面研究和该前体的可能性能。

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