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通过控制尺寸和位置将金属纳米粒子固定在金属有机骨架上,以优化催化性能。

Immobilizing metal nanoparticles to metal-organic frameworks with size and location control for optimizing catalytic performance.

机构信息

National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka 563-8577, Japan.

出版信息

J Am Chem Soc. 2013 Jul 17;135(28):10210-3. doi: 10.1021/ja403330m. Epub 2013 Jul 2.

Abstract

AuNi alloy nanoparticles were successfully immobilized to MIL-101 with size and location control for the first time by double solvents method (DSM) combined with a liquid-phase concentration-controlled reduction strategy. When an overwhelming reduction approach was employed, the uniform 3D distribution of the ultrafine AuNi nanoparticles (NPs) encapsulated in the pores of MIL-101 was achieved, as demonstrated by TEM and electron tomographic measurements, which brings light to new opportunities in the fabrication of ultrafine non-noble metal-based NPs throughout the interior pores of MOFs. The ultrafine AuNi alloy NPs inside the mesoporous MIL-101 exerted exceedingly high activity for hydrogen generation from the catalytic hydrolysis of ammonia borane.

摘要

首次通过双溶剂法(DSM)结合液相浓度控制还原策略,成功地将 AuNi 合金纳米颗粒固定在 MIL-101 上,实现了尺寸和位置的控制。当采用压倒性的还原方法时,通过 TEM 和电子断层扫描测量,实现了封装在 MIL-101 孔中的超细 AuNi 纳米颗粒(NPs)的均匀 3D 分布,这为在 MOFs 的内部孔中制造超细非贵金属基 NPs 带来了新的机遇。介孔 MIL-101 内的超细 AuNi 合金 NPs 在氨硼烷催化水解制氢反应中表现出极高的活性。

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