Fu Yufang, Zhu Ziqian, Chen Yunhong, Liu Chuang, Wang Ganping, Rong Youqi, Liang Kun, Mei Bingbao, Fang Jian, Zhao Jihua
School of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, 730000, PR China.
Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201800, PR China.
Chemistry. 2025 Feb 17;31(10):e202403624. doi: 10.1002/chem.202403624. Epub 2025 Jan 26.
Dual single-atom catalysts have attracted considerable research interest due to their higher metal atom loading and more flexible active sites compared to single-atom catalysts (SACs). We pioneered the one-step synthesis of sheets copper-cobalt graphitic carbon nitride dual single-atom (S-Cu/Co-g-CN) using folding fan-shaped aluminum foil as a template, and used them as catalysts in the epoxidation of styrene respectively. Through XAFS (X-ray Absorption Fine Structure) and other characterizations, it is found that Cu and Co single atoms are stabilized separately on g-CN via coordination with nitrogen (N), hindered the ordered growth of sheets, and formed more pore structures, which not only increased more catalytically active sites, but also effectively prevented the flakes re-aggregate during the catalytic process. And the synergistic effect between Cu and Co changes the energy band structure of the material and facilitates electron transfer during catalysis, hence an excellent catalytic effect of 89 % styrene conversion and 85 % styrene oxide selectivity was achieved when S-Cu/Co-g-CN-1 : 1 was applied in the epoxidation of styrene. Furthermore, the mechanisms of the epoxidation of styrene with S-Cu/Co-g-CN-1 : 1 was probed by the density functional theory (DFT) based on the slab model.
与单原子催化剂(SACs)相比,双单原子催化剂因其更高的金属原子负载量和更灵活的活性位点而引起了广泛的研究兴趣。我们率先以折扇状铝箔为模板,一步合成了片状铜钴石墨相氮化碳双单原子催化剂(S-Cu/Co-g-CN),并将其分别用作苯乙烯环氧化反应的催化剂。通过X射线吸收精细结构(XAFS)等表征发现,Cu和Co单原子通过与氮(N)配位分别稳定在g-CN上,阻碍了片层的有序生长,并形成了更多的孔结构,这不仅增加了更多的催化活性位点,还有效防止了薄片在催化过程中重新聚集。而且Cu和Co之间的协同作用改变了材料的能带结构,促进了催化过程中的电子转移,因此当S-Cu/Co-g-CN-1:1用于苯乙烯环氧化反应时,实现了89%的苯乙烯转化率和85%的环氧苯乙烷选择性的优异催化效果。此外,基于平板模型,利用密度泛函理论(DFT)探究了S-Cu/Co-g-CN-1:1催化苯乙烯环氧化反应的机理。