硅醇
沸石
微型多孔材料
介孔材料
化学
热稳定性
烷基
分子筛
化学工程
钙长石
硅酸铝
分子
结晶学
介孔有机硅
混合材料
纳米技术
催化作用
MCM-41
X射线晶体学
插层(化学)
晶体结构
密度泛函理论
金属有机骨架
电子衍射
粉末衍射
热处理
衍射
复合数
结晶度
材料科学
上部结构
作者
Aimin Gong,Chenyang Nie,Haodi Ding,Cailing Chen,Qiang Zhang,Guangyuan He,Xilin Jia,Nairui Liu,Tianpeng Li,Yecheng Li,Zijiang Jiang,Donghai Mei,Yu Han,Peng Guo,Fengqian Chen,Jihong Yu
摘要
Expanding the pore size of zeolites beyond the microporous regime has long been constrained by conventional organic structure-directing agents (OSDAs). Here we report JU-69, a mesoporous pure-silica zeolite featuring one-dimensional 36-ring channels, which represent the largest apertures observed in any tetrahedral framework, and an ultralow framework density (9.53 T/1000 Å3). A surfactant-like phosphonium OSDA, combining bulky head groups with a long alkyl chain, directs the formation of columnar assemblies that template long-range-ordered mesoporous walls. Three-dimensional electron diffraction reveals a trigonal framework constructed from three composite building units (CBUs), including two previously unknown CBUs that generate chiral clover motifs and circular 36-ring pores. JU-69 shows outstanding stability up to 900 ℃ and hosts periodically arranged silanol groups ideal for metal anchoring, exemplified by active Pd/JU-69 hydrogenation catalysts. This work establishes a new pathway for designing crystalline mesoporous zeolites with unprecedented structural openness.
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