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Interfacial Effects in Iron-Nickel Hydroxide-Platinum Nanoparticles Enhance Catalytic Oxidation

This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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Abstract

该研究工作是在郑南峰教授的领导下,由校内外、国内外多个课题组共同努力,历时三年完成。郑南峰、傅钢、陈明树等三个课题组紧密协作负责催化剂的合成、表征、性能测试以及催化机理研究;中国科学院物理研究所谷林研究员主要负责纳米颗粒的亚埃级球差校正高分辨透射电子显微研究;加拿大达尔豪斯大学化学系的张鹏教授课题组和台湾同步辐射研究中心李志甫研究员等参与催化剂的同步辐射X-射线吸收光谱研究。 该工作受到了国家自然科学基金委、科技部、厦门大学、固体表面物理化学国家重点实验室、能源材料化学协同创新中心以及醇醚酯化工清洁生产国家工程实验室的资助与支持。 ; Hybrid metal nanoparticles can allow separate reaction steps to occur in close proximity at different metal sites and accelerate catalysis. We synthesized iron-nickel hydroxide–platinum (transition metal-OH-Pt) nanoparticles with diameters below 5 nanometers and showed that they are highly efficient for carbon monoxide (CO) oxidation catalysis at room temperature. We characterized the composition and structure of the transition metal–OH-Pt interface and showed that Ni2+ plays a key role in stabilizing the interface against dehydration. Density functional theory and isotope-labeling experiments revealed that the OH groups at the Fe3+-OH-Pt interfaces readily react with CO adsorbed nearby to directly yield carbon dioxide (CO2) and simultaneously produce coordinatively unsaturated Fe sites for O2 activation. The oxide-supported PtFeNi nanocatalyst rapidly and fully removed CO from humid air without decay in activity for 1 month.