催化作用
八面体
化学
Atom(片上系统)
扫描电子显微镜
扫描透射电子显微镜
同种类的
光谱学
透射电子显微镜
结晶学
能量色散X射线光谱学
材料科学
物理化学
晶体结构
纳米技术
有机化学
热力学
量子力学
计算机科学
复合材料
嵌入式系统
物理
作者
Zhe Tan,Masaaki Haneda,Hiroshi Kitagawa,Bo Huang
标识
DOI:10.1002/anie.202202588
摘要
This study provided an effective strategy to construct dual-atom sites by solid-solution alloying. A slow synthesis methodology was established for the solid-solution preparations as dual-atom-site catalysts. The atomic-level homogeneous Pdx Rh1-x dual-atom-site catalysts were successfully synthesized over the whole composition range, as evidenced by X-ray powder diffraction and scanning transmission electron microscope energy-dispersive X-ray spectroscopy mapping measurements. The challenging morphology formation in the immiscible alloys was achieved by an energy-controlling process as the octahedral Rh-rich alloys. The Pd0.3 Rh0.7 dual-atom-site catalyst had unique surface states to activate the key reactants of CO and NO in the complex three-way catalytic reactions, and it performed significantly better than pure Rh.
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