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Extended Brewer hypo-hyper-d-interionic bonding theory II. Strong metal-support interaction grafting of composite electrocatalysts

机译:扩展的Brewer次-d-超离子键合理论II。复合电催化剂的强金属-载体相互作用接枝

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The extended Brewer interactive interionic bonding theory (EBIIBT) to show the equivalence of interatomic and interionic bonding features, as the prerequisite for selective strong metal-support interactive (SMSI) grafting of metallic nanostructured catalyst upon active center of individual and composite hypo-d-electronic oxide supports was presented in the preceding part of the same study (Int. J. Hydrogen Energy). SMSI of both individual and composite, prevailingly hyper-d-electronic metallic electrocatalysts upon individual and/or composite, usually hypo-d-electronic oxide substrates, has been employed to create and graft (anchor) bifunctional electrocatalysts for simultaneous anodic hydrogen and CO oxidation in low temperature PEM (polymer exchange membrane) fuel cells (LT PEM FC), or at least for advanced CO tolerance. The selective interionic bonding method upon predestined active centers of hypo-d-electronic oxide supports has been adapted to graft (anchor) directly a priori defined nanosized intermetallic phases and synergetic bifunctional electrocatalysts from decomposition of corresponding stoichiometric mixtures of various individual or intermetallic acetylacetonates (2, 4-pentanedionates). An adapted TG method based on TPR has been properly used to test, define, control and stimulate the homogeneity of the intermetallic crystal cluster bonding and growth of nanostructured composite catalysts, mostly composed of rather extra stable Brewer type Laves fcc phases, formerly being grafted as interactive composite mixtures of 2,4-pentanedionate nanosized precursors upon proper SMSI hypo-d-interelectronic oxide supports. Their resulting bifunctional electrocatalytic properties are displayed and discussed. Thus, it has been pointed out that the term SMSI has primarily a broader hypo-hyper-d-interelectronic interactive sense in both the bonding effectiveness and bifunctional catalytic meaning, and in fact stays in the core of such extended Brewer interionic bonding theory.
机译:扩展的Brewer相互作用离子间键合理论(EBIIBT)证明了原子间键合和离子间键合特征的等效性,这是在单个和复合低d-d-活性中心上进行金属纳米结构催化剂的选择性强金属-载体相互作用(SMSI)接枝的先决条件在同一研究的前一部分中介绍了电子氧化物载体(Int。J. Hydrogen Energy)。在单个和/或复合材料(通常为次d-电子氧化物)底物上的单个和复合(主要是超d电子金属)电催化剂的SMSI已用于创建和接枝(锚定)双功能电催化剂,以同时进行阳极氢和CO氧化在低温PEM(聚合物交换膜)燃料电池(LT PEM FC)中使用,或至少用于提高CO耐受性。在预定的次电子氧化物载体的预定活性中心上的选择性离子键合方法已被适配为直接将先验定义的纳米级金属间相和协同双功能电催化剂从各种单独的或金属间的乙酰丙酮化物的相应化学计量混合物的分解接枝(锚定)(2 ,4-戊二酸酯)。一种基于TPR的改进的TG方法已被正确地用于测试,定义,控制和促进金属间晶体簇键合的均质性以及纳米结构复合催化剂的生长,这些催化剂主要由相当稳定的Brewer型Laves fcc相组成,以前被接枝为适当的SMSI hypo-d-inter-interelectronic氧化物载体上的2,4-戊二酮酸酯纳米尺寸前体的交互式复合混合物。显示并讨论了它们产生的双功能电催化性能。因此,已经指出,术语SMSI在键合效力和双功能催化意义上都主要具有较宽泛的hyper-d-d-电子相互作用的含义,并且实际上仍然是这种扩展的Brewer离子键理论的核心。

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