Facile functionalization iron in zeolitic imidazole framework-67 under solvent-free conditions for enhancing CO 2 fixation reaction

被引:2
|
作者
Ma, Dandan [1 ,2 ]
Cheng, Zhonghan [3 ,4 ]
Yuan, Ye [3 ]
Chaemchuen, Somboon [3 ,5 ]
机构
[1] Changzhi Med Coll, Dept Pharm, Changzhi 046000, Shanxi, Peoples R China
[2] Changzhi Med Coll, Stem Cell & Tissue Engn Res Ctr, Changzhi 046000, Shanxi, Peoples R China
[3] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[4] Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Peoples R China
[5] Mahidol Univ, Fac Engn, Dept Chem Engn, Nakhon Pathom 73170, Thailand
关键词
Heterometal; ZIFs; Solid-state thermal method; CO2; cycloaddition; In-situ thermal metho; METAL-ORGANIC FRAMEWORKS; EFFICIENT HETEROGENEOUS CATALYST; PHOTOCATALYTIC DEGRADATION; CHEMICAL FIXATION; CRYSTAL-GROWTH; ZIF-67;
D O I
10.1016/j.micromeso.2024.113161
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The heterometal functionalization on zeolitic-imidazole frameworks (ZIFs) is a strategy to modify properties over the homometal ZIFs. A green strategy for simultaneously functionalized iron atoms during the crystal formation of ZIF-67 (Fe@ZIF-67) through the solid -solid thermal (SST) method is newly developed. The single-step process and absent solvent conditions are beneficial advantages of this SST method over the early reported synthetic methods. The results show that the iron is well -dispersed and homogeneously coordinated in the structure of Fe@ZIF-67. Moreover, the optimal iron-functionalized ZIF-67 (20Fe@ZIF-67) significantly enhances the catalytic performance of CO 2 cycloaddition epoxide by 2.3 times compared to pristine ZIF-67 under mild reaction conditions. The DFT calculation reveals that the iron atom induces the unsaturated sites or defect structure on the Fe@ZIF-67 catalyst, providing more reactive sites for the catalytic activity of the reaction.
引用
收藏
页数:10
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