催化作用
钴
化学
选择性
混合(物理)
化学工程
聚合物
组合化学
甲烷
纳米技术
多相催化
材料科学
作者
Wei Fang,Yu Hui,Yuhui Chen,Jindi Duan,Hangjie Li,Yuqiu Deng,Chijin Zhang,G. Leendert Bezemer,Peter Munnik,Songqiang Zhu,Weiming Teng,Zhangmin Wang,Yifeng Zhu,Shengqi Chu,Du Guo-Hao,Lina Li,Siyu Yao,Wentao Yuan,Zuwei Liao,Ying Jiang
标识
DOI:10.1038/s41467-026-76571-8
摘要
Cobalt catalysts have been widely studied for Fischer-Tropsch synthesis, yet they gradually deactivate under water-rich reaction conditions. Current stabilization strategies rely on complex catalyst compositions or even use noble-metal promoters. Here, we demonstrate that cobalt deactivation can be effectively hindered by physically regulating water diffusion. By physical mixing of a classical Co/SiO2 catalyst with hydrophobic polydivinylbenzene, a microenvironment is created that promotes directional water transport away from the cobalt. As a result, stable Fischer-Tropsch operation is achieved for 1200 hours, maintaining high activity with 88-90% selectivity toward C5+ hydrocarbons, minimal methane and CO2 production. Mechanistic investigations suggest that the combination of hydrophobic polymer could promote directional water removal from the catalyst surface. These findings demonstrate a practical strategy for stabilizing highly water-sensitive catalysts. Cobalt catalysts are widely used for Fischer–Tropsch synthesis but gradually deactivate under water-rich reaction conditions. Here, the authors demonstrate a practical strategy to stabilize these water-sensitive catalysts by regulating water diffusion.
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