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Exploring surface science and restructuring in reactive atmospheres of colloidally prepared bimetallic CuNi and CuCo nanoparticles on SiO2in situ using ambient pressure X-ray photoelectron spectroscopy

机译:使用环境压力X射线光电子能谱法在SiO2上原位研究在SiO2上胶态制备的双金属CuNi和CuCo纳米粒子的反应科学中的表面科学和重组

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摘要

Bimetallic nanoparticles (∼11 nm diameter) of CuNi and CuCo were prepared by a new synthetic route and the 1 :1 atomic ratio of their constituent elements confirmed using STEM-EDS at a single particle level. These nanoparticles, supported on the native oxide layer of a silicon wafer, were studied in situ in a series of reactive gas atmospheres (H2 → CO or CO/H2 → O2 → H2) using ambient pressure X-ray photoelectron spectroscopy (AP-XPS). Despite the deliberate similarity of nickel and cobalt with respect to copper, their restructuring behaviour is different. CuNi nanoparticles were found to surface segregate nickel in H2, but copper in O2 reversibly, while CuCo nanoparticles were found to surface segregate copper irreversibly when exposed to O2, such that the surface remains copper rich when re-exposed to H2. Both systems also restructure in opposition to the behaviour predicted by the surface free energies and enthalpies of oxide formation of the elements from which they are comprised-factors that are seen to control restructuring and surface segregation in many similar systems. © 2013 The Royal Society of Chemistry.
机译:通过新的合成路线制备了CuNi和CuCo的双金属纳米粒子(直径约11 nm),并使用STEM-EDS在单个粒子水平上证实了其构成元素的原子比为1:1。使用环境压力X射线光电子能谱(AP-XPS)在一系列反应性气体气氛(H2→CO或CO / H2→O2→H2)中原位研究了负载在硅片天然氧化物层上的这些纳米颗粒)。尽管镍和钴在铜方面有故意相似性,但它们的重组行为却有所不同。发现CuNi纳米颗粒使H2中的镍表面偏析,但O2中的铜可逆地偏析,而发现CuCo纳米颗粒在暴露于O2时不可逆地偏析铜,因此当再次暴露于H2时,表面仍富含铜。两种系统的结构也与表面自由能和构成它们的元素的氧化物形成的焓所预测的行为相反,在许多相似的系统中,这些因素被认为可控制结构和表面偏析。 ©2013皇家化学学会。

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