格式化
催化作用
化学
吸收(声学)
傅里叶变换红外光谱
光化学
材料科学
化学工程
有机化学
工程类
复合材料
作者
Guangjun Ji,Cunyao Li,Benhan Fan,Guoqing Wang,Zhao Sun,Miao Jiang,Lei Ma,Yan Li,Yunjie Ding
标识
DOI:10.1021/acscatal.3c05214
摘要
Hydrogenation of CO2, an abundant C1 resource, into formate, is one of the most charming utilization routes of CO2. Herein, a series of single Ru–P site catalysts coupling N sites (denoted as Ru/P&N-POPs) were designed and applied in the highly effective hydrogenation of CO2 to formate. The Ru (II) ions were firmly anchored and finely regulated by P sites in the polymeric skeleton, while the original N species surrounding single Ru–P active sites enriched and activated CO2. Besides, 13C{1H} R-type RF irradiation and two-dimensional separated local field (2D R-SLF) experiments proved the good flexibility of P&N-POPs frameworks, which were beneficial for optimizing the orientation of functional sites and the synergy of abundant Ru–P active species and N species. As a result, a ca. 2000 h–1 TOF of CO2 and at least 5 recycles were achieved in the formate synthesis under 393 K and 6.0 MPa (CO2/H2 = 1:1). Multiple characterization methods including mass nuclear magnetic resonance, extended X-ray absorption fine structure, scanning transmission electron microscopy, in situ Fourier transform infrared, etc. were employed to reveal the mechanism for the catalytic performance of Ru/P&N-POPs.
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