贵金属
材料科学
纳米颗粒
透射电子显微镜
扫描透射电子显微镜
金属
乙炔
惰性气体
色散(光学)
碳纤维
纳米技术
化学工程
化学物理
分析化学(期刊)
化学
冶金
复合材料
工程类
有机化学
物理
光学
复合数
色谱法
作者
Shengjie Wei,Ang Li,Jincheng Liu,Zhi Li,Wenxing Chen,Yue Gong,Qinghua Zhang,Weng‐Chon Cheong,Yu Wang,Lirong Zheng,Hai Xiao,Chen Chen,Dingsheng Wang,Qing Peng,Lin Gu,Xiaodong Han,Jun Li,Yadong Li
标识
DOI:10.1038/s41565-018-0197-9
摘要
Single noble metal atoms and ultrafine metal clusters catalysts tend to sinter into aggregated particles at elevated temperatures, driven by the decrease of metal surface free energy. Herein, we report an unexpected phenomenon that noble metal nanoparticles (Pd, Pt, Au-NPs) can be transformed to thermally stable single atoms (Pd, Pt, Au-SAs) above 900 °C in an inert atmosphere. The atomic dispersion of metal single atoms was confirmed by aberration-corrected scanning transmission electron microscopy and X-ray absorption fine structures. The dynamic process was recorded by in situ environmental transmission electron microscopy, which showed competing sintering and atomization processes during NP-to-SA conversion. Further, density functional theory calculations revealed that high-temperature NP-to-SA conversion was driven by the formation of the more thermodynamically stable Pd-N4 structure when mobile Pd atoms were captured on the defects of nitrogen-doped carbon. The thermally stable single atoms (Pd-SAs) exhibited even better activity and selectivity than nanoparticles (Pd-NPs) for semi-hydrogenation of acetylene.
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