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Boosting CO2 hydrogenation of Fe-based monolithic catalysts via 3D printing technology-induced heat/mass-transfer enhancements

催化作用 传质 材料科学 解吸 化学工程 制作 吸附 纳米技术 选择性 化学 有机化学 医学 替代医学 色谱法 病理 工程类
作者
Yang Wang,Shiyuan Lin,Meng Li,Chuanyong Zhu,Hao Yang,Pei Dong,Mingjie Lu,Wenhang Wang,Jianlin Cao,Qiang Liu,Xiang Feng,Han Hu,Noritatsu Tsubaki,Mingbo Wu
出处
期刊:Applied Catalysis B-environmental [Elsevier]
卷期号:340: 123211-123211 被引量:30
标识
DOI:10.1016/j.apcatb.2023.123211
摘要

The direct transformation of CO2 into valuable chemicals with the aid of sustainable energy-generated H2 has attracted enormous interest owing to the integrated functions of carbon elimination and non-fossil fuel-derived products supply. As one of the most promising catalysts for CO2 hydrogenation, the chemical properties of Fe-based catalysts, such as electronic structure and coordination environment, have been widely studied. However, the mass/heat transfer effects in Fe-based catalysts are also crucial to the targeted product selectivity and catalytic stability, but have been rarely investigated due to the lack of facile fabrication protocols. Herein, we precisely fabricate and tailor the architecture of the Fe-based monolithic catalysts by a direct ink writing (DIW)-type three-dimensional (3D) printing technology under the guidance of the computationally controlled printing procedure. The Fe-based monolithic catalyst with spiral-type architecture delivers extremely high light olefins selectivity (52.6%) and space time yield (STY, 451.8 gCH2 kgcat−1 h−1) from CO2 hydrogenation. Based on the mass-transfer simulation, the spiral-structured channels in the Fe-based monolithic catalyst lower the coverage of intermediates and products on the catalytic interface due to the optimal mass-transfer effect, thus maximizing the utilization of active sites and timely terminating the carbon-chain growth. More in-depth, the density functional theoretical (DFT) simulations verify that the relatively electron-rich catalytic interface with low intermediate coverage could facilitate the desorption of olefins and decelerate the C-C coupling step, which synergistically guarantee the enhanced light olefins synthesis performance. Furthermore, the enhanced heat-transfer effect endowed by the 3D architecture prolongs the life-time of catalyst by avoiding undesirable active site aggregation and carbon deposition. The powerful strategy for catalyst fabrication not only provides a new concept of regulating the CO2 hydrogenation performance of Fe-based catalysts but also holds a great promise to spread into other catalytic systems for targeted synthesis.
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