催化作用
材料科学
煅烧
纳米颗粒
惰性气体
惰性
金属
化学工程
苯乙烯
氧化物
无机化学
纳米技术
有机化学
冶金
化学
共聚物
聚合物
工程类
复合材料
作者
Shiguang Mo,Wentong Jing,Weijie Zhang,Kunlong Liu,Binghui Wu,Ruixuan Qin,Nanfeng Zheng
标识
DOI:10.1007/s40843-022-2429-6
摘要
Supported ultrafine metal nanoparticles display outstanding catalytic performance in heterogeneous catalysis. Nevertheless, there are limited convenient and practical approaches for synthesizing supported ultrafine metal nanoparticle catalysts, despite the development of advanced fabrication methods. High-temperature reduction is often required for the preparation of metal catalysts for catalytic hydrogenation. However, the use of reductants, such as H2, easily leads to the aggregation of nanoparticles during catalyst preparation. In this work, we developed an effective self-reduction strategy using Pd precursors with organic ligands to prepare supported ultrafine Pd catalysts. Simple calcination under an inert atmosphere leads to the formation of uniform and ultrafine Pd nanoparticles (∼1 nm). These Pd precursors were reduced following the reaction between the −CHx groups on ligands and surface hydroxyl species on oxide supports. CO and oxygen vacancies generated in situ both contributed to the stabilization of ultrafine Pd nanoparticles. The as-prepared ultrafine Pd nanoparticles were highly stable even after the high-temperature treatment at 600°C. The catalysts displayed a turnover frequency as high as 26,910 h−1 for styrene hydrogenation and maintained the catalytic activity for at least 5 test cycles.
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