脱氢
丙烷
催化作用
化学
铂金
类型(生物学)
无机化学
有机化学
生态学
生物
作者
Longkang Zhang,Xinyu Chen,Yue Ma,Shaojia Song,Hao Xu,Yejun Guan,Weiyu Song,Jiangwei Zhang,Peng Wu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-06-07
卷期号:14 (12): 9431-9439
被引量:8
标识
DOI:10.1021/acscatal.4c02091
摘要
Single atom catalysts have been widely studied due to their high metal dispersity and remarkable catalytic performance. However, stabilizing single-atom metals remains challenging because of the high surface free energy. In this work, framework Fe atom-stabilized single atom Pt were successfully confined into MWW zeolite (Pt@Fe-MWW) by a one-pot synthesis strategy. The isolated skeleton Fe served as anchoring site and promoter to stabilize the single atom Pt via Pt–O–Fe coordination as identified by the in situ CO-IR spectra and XAFS analysis, enabling Pt@Fe-MWW with satisfied activity for the PDH reaction with trace Pt content (<0.01 wt %). A linear relationship between the quantities of Pt–O–Fe coordinated species and the propylene formation rate further confirmed the synergistic catalysis of Pt and skeleton Fe species. A recorded propylene formation rate of Pt (FRC3H6/Pt) of 1100 mol/gPt/h was achieved with a Pt content of 0.006 wt %. DFT calculations revealed that the formation of Pt–O–Fe species reduced the dissociation energy of the C–H bonds and facilitated the desorption of H2, enabling efficient propane dehydrogenation.
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