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Solid frustrated-Lewis-pair catalysts constructed by regulations on surface defects of porous nanorods of CeO2

机译:根据CeO2多孔纳米棒表面缺陷的规定构造的固态沮丧-刘易斯对催化剂

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摘要

Identification on catalytic sites of heterogeneous catalysts at atomic level is important to understand catalytic mechanism. Surface engineering on defects of metal oxides can construct new active sites and regulate catalytic activity and selectivity. Here we outline the strategy by controlling surface defects of nanoceria to create the solid frustrated Lewis pair (FLP) metal oxide for efficient hydrogenation of alkenes and alkynes. Porous nanorods of ceria (PN-CeO2) with a high concentration of surface defects construct new Lewis acidic sites by two adjacent surface Ce3+. The neighbouring surface lattice oxygen as Lewis base and constructed Lewis acid create solid FLP site due to the rigid lattice of ceria, which can easily dissociate H–H bond with low activation energy of 0.17 eV.
机译:在原子水平上鉴定多相催化剂的催化位点对于理解催化机理很重要。金属氧化物缺陷的表面工程可以构建新的活性位点,并调节催化活性和选择性。在这里,我们概述了通过控制纳米二氧化铈的表面缺陷以创建固体沮丧的路易斯对(FLP)金属氧化物来有效加氢烯烃和炔烃的策略。具有高浓度表面缺陷的氧化铈多孔纳米棒(PN-CeO2)通过两个相邻的表面Ce 3 + 构成新的Lewis酸性位点。相邻的表面晶格氧(作为路易斯碱)和构造的路易斯酸由于二氧化铈的刚性晶格而形成了固态FLP位点,可以很容易地以0.17 eV的低活化能使H-H键解离。

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