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First-principles study of the products of CO_2 dissociation on nickel-based alloys: Trends in energetics with alloying element

机译:镍基合金上CO_2分解产物的第一性原理研究:含合金元素的高能态趋势

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Oxidation and corrosion of nickel and Ni-based alloys are a problem for many industrial applications, such as power plants that use supercritical CO2 as the working fluid. In supercritical CO2 environments, CO2 dissociates on the surface forming adsorbed CO and 0, which can oxidize the surface. The adsorbed CO can further breakdown via direct CO dissociation or via the Boudouard reaction to form adsorbed C, which can in turn carburize the surface. Understanding how the adsorbed species interact with different Ni-based alloys can help guide the design of future alloys. The interactions of adsorbed 0, C, and CO on the (100) and (111) facets of pure Ni and Ni individually alloyed with AI, Co, Cr, Cu, Fe, Mn, Mo, Nb, Ti, V, and W are examined using density functional theory. We find that the binding of CO is energetically similar across all alloy surfaces and both facets, while 0 binding varies strongly with different metals added to nickel and C binding varies between the different facets but only slightly for different metals alloyed to nickel. The binding of 0 is weaker on pure Ni and Ni alloyed with Cu, Co, Fe, Al, or Mn and stronger on Ni alloyed with Nb, Cr, Mo, Ti, V, or W, while the binding of C is weaker on the (111) facet than the (100) facet. The difference in the binding energies of the adsorbates across the different alloy surfaces is due mainly to the ensemble effect, rather than the ligand effect. The thermodynamics of CO breakdown are also studied and we find that the breakdown of CO via direct CO dissociation is endothermic on the (111) facet and exothermic on the (100) facet, with the alloy surfaces that bind 0 strongly having the most exothermic reaction energies. The breakdown of CO via the Boudouard reaction has similar reaction energies across the different alloy surfaces of a single facet and is endothermic on both facets, with the (111) facet being most endothermic. This comprehensive study presents a summary of the current literature as well as a well-rounded view of the products of CO2 breakdown on Ni surfaces alloyed with the most common alloying elements used in industrial applications.
机译:镍和镍基合金的氧化和腐蚀对于许多工业应用都是一个问题,例如使用超临界CO2作为工作流体的发电厂。在超临界CO2环境中,CO2在表面解离,形成吸附的CO和0,这会氧化表面。吸附的CO可以通过直接的CO解离或通过Boudouard反应进一步分解,形成吸附的C,从而使表面渗碳。了解被吸附物质如何与不同的镍基合金相互作用将有助于指导未来合金的设计。纯Ni和分别与AI,Co,Cr,Cu,Fe,Mn,Mo,Nb,Ti,V和W合金化的纯Ni和Ni的(100)和(111)面上的吸附的0,C和CO的相互作用使用密度泛函理论进行检验。我们发现,在所有合金表面和两个小平面上,CO的结合在能量上都相似,而0结合随添加到镍中的不同金属而变化很大,而C的结合在不同小面之间变化,但对于与镍合金化的不同金属仅略有变化。在纯的Ni和与Cu,Co,Fe,Al或Mn合金化的Ni上,0的结合较弱,而在与Nb,Cr,Mo,Ti,V或W合金化的Ni上的0的结合较弱,而C的在C的结合上较弱(111)面比(100)面。跨越不同合金表面的被吸附物结合能的差异主要是由于整体效应而不是配体效应。还研究了CO击穿的热力学,我们发现通过直接CO分解引起的CO击穿在(111)面上是吸热的,而在(100)面上是放热的,结合0的合金表面放热反应最强能量。通过Boudouard反应分解的CO在单面的不同合金表面上具有相似的反应能,并且在两个面上都是吸热的,(111)面上的吸热最大。这项全面的研究提供了最新文献的摘要,以及对与工业应用中最常见的合金元素合金化的Ni表面上的CO2分解产物的全面了解。

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