Author
Listed:
- Baojian Zhang
(Central China Normal University
Central China Normal University
Wuhan Institute of Photochemistry and Technology)
- Rui Liu
(Central China Normal University
Central China Normal University
Wuhan Institute of Photochemistry and Technology)
- Liangwei Li
(Central China Normal University
Central China Normal University
Wuhan Institute of Photochemistry and Technology)
- Weihong Guo
(Central China Normal University
Central China Normal University
Wuhan Institute of Photochemistry and Technology)
- Biluan Zhang
(Central China Normal University
Central China Normal University)
- Bosheng Chen
(Central China Normal University
Central China Normal University)
- Weidong Yuan
(Central China Normal University
Central China Normal University)
- Pan Li
(Central China Normal University
Central China Normal University
Wuhan Institute of Photochemistry and Technology)
- Shaowen Zhang
(Central China Normal University
Central China Normal University)
- Jinlong Wang
(Central China Normal University
Central China Normal University
Wuhan Institute of Photochemistry and Technology)
- Ji Yang
(Central China Normal University
Central China Normal University
Wuhan Institute of Photochemistry and Technology)
- Zhu Luo
(Central China Normal University
Central China Normal University
Wuhan Institute of Photochemistry and Technology)
- Yanbing Guo
(Central China Normal University
Central China Normal University
Wuhan Institute of Photochemistry and Technology)
Abstract
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.
Suggested Citation
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, 2025.
"Ultra-stable low-coordinated PtSA/CeZrO2 ordered macroporous structure integrated industrial-scale monolithic catalysts for high-temperature oxidation,"
Nature Communications, Nature, vol. 16(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63112-y
DOI: 10.1038/s41467-025-63112-y
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