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Atomic-scale engineering of indium oxide promotion by palladium for methanol production via CO2 hydrogenation

机译:钯通过CO2氢化甲醇生产氧化铟促进原子尺度工程

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Metal promotion is broadly applied to enhance the performance of heterogeneous catalysts to fulfill industrial requirements. Still, generating and quantifying the effect of the promoter speciation that exclusively introduces desired properties and ensures proximity to or accommodation within the active site and durability upon reaction is very challenging. Recently, Insub2/subOsub3/sub was discovered as a highly selective and stable catalyst for green methanol production from COsub2/sub. Activity boosting by promotion with palladium, an efficient Hsub2/sub-splitter, was partially successful since palladium nanoparticles mediate the parasitic reverse water-gas shift reaction, reducing selectivity, and sinter or alloy with indium, limiting metal utilization and robustness. Here, we show that the precise palladium atoms architecture reached by controlled co-precipitation eliminates these limitations. Palladium atoms replacing indium atoms in the active Insub3/subOsub5/sub ensemble attract additional palladium atoms deposited onto the surface forming low-nuclearity clusters, which foster Hsub2/sub activation and remain unaltered, enabling record productivities for 500?h.
机译:广泛应用金属促销以增强异质催化剂的性能以满足工业要求。仍然,产生和量化启动子形态的效果专门引入所需性质并确保在活性位点内的接近或在反应时耐久性非常具有挑战性。最近,在<亚> 2 O 3 中被发现为来自CO 2 的绿色甲醇生产的高选择性和稳定的催化剂。通过促进钯,一种有效的H 2 -splitter,促进促进的活性促进,因为钯纳米粒子介导寄生反转水 - 气体移位反应,减少选择性和烧结剂或用铟,限制金属利用和鲁棒性。在这里,我们表明受控共沉淀达到的精确钯原子架构消除了这些限制。钯原子替代活性的铟原子在 3 O 5 集合中吸引沉积在表面形成低核簇上的额外钯原子,这使得H 2 激活并保持不变,使得能够为500?h的记录产品。

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