催化作用
材料科学
化学工程
比例(比率)
纳米技术
化学
有机化学
量子力学
物理
工程类
作者
Baojian Zhang,Rui Liu,Liangwei Li,Weihong Guo,Biluan Zhang,Bosheng Chen,Weidong Yuan,Pan Li,Shaowen Zhang,Jinlong Wang,Ji Yang,Zhu Luo,Yanbing Guo
标识
DOI:10.1038/s41467-025-63112-y
摘要
Platinum-group metals (Pt) commonly used in thermal catalytic processes often suffer from catalyst deactivation, such as Pt sintering, Pt overoxidation, and Pt loss under high-temperature conditions. To address these, we present a novel PtSA/CeZrO2 catalyst, featuring isolated Pt single atoms (PtSA) on a Ce0.8Zr0.2O2 support with an ordered macroporous (OM) structure. Firstly, Zr-stabilized dynamic low-coordinated PtSA releases more free d-electrons by reducing Pt-O bond occupation, thereby preserving peroxide activity at high temperatures and enhancing propane C-H activation. Additionally, the OM structure prevents Pt loss and reduces Pt loading to 0.4 gPt/L, compared with 0.9 gPt/L in commercial diesel oxidation catalysts. As a result, the PtSA/CeZrO2 maintains 92% conversion at 450 °C even after 50 h aging at 800 °C with 10 vol.% H2O. Finally, the catalyst is integrated into a 3.4-liter commercial cordierite monolith for developing and scaling robust catalytic converters.
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