1] Inorganic and Structural Chemistry, Department of Materials and Environmental Chemistry, Stockholm University, SE-106 91 Stockholm, Sweden [2] Berzelii Centre EXSELENT on Porous Materials, Stockholm University, SE-106 91 Stockholm, Sweden.
Centre for Ordered Nanoporous Materials Synthesis, School of Environmental Science and Engineering, POSTECH, Pohang 790-784, South Korea.
Nature. 2015 Aug 6;524(7563):74-8. doi: 10.1038/nature14575. Epub 2015 Jul 15.
The prediction and synthesis of new crystal structures enable the targeted preparation of materials with desired properties. Among porous solids, this has been achieved for metal-organic frameworks, but not for the more widely applicable zeolites, where new materials are usually discovered using exploratory synthesis. Although millions of hypothetical zeolite structures have been proposed, not enough is known about their synthesis mechanism to allow any given structure to be prepared. Here we present an approach that combines structure solution with structure prediction, and inspires the targeted synthesis of new super-complex zeolites. We used electron diffraction to identify a family of related structures and to discover the structural 'coding' within them. This allowed us to determine the complex, and previously unknown, structure of zeolite ZSM-25 (ref. 8), which has the largest unit-cell volume of all known zeolites (91,554 cubic ångströms) and demonstrates selective CO2 adsorption. By extending our method, we were able to predict other members of a family of increasingly complex, but structurally related, zeolites and to synthesize two more-complex zeolites in the family, PST-20 and PST-25, with much larger cell volumes (166,988 and 275,178 cubic ångströms, respectively) and similar selective adsorption properties. Members of this family have the same symmetry, but an expanding unit cell, and are related by hitherto unrecognized structural principles; we call these family members embedded isoreticular zeolite structures.
新晶体结构的预测和合成能够有针对性地制备具有所需性质的材料。在多孔固体中,这已经在金属有机骨架中实现,但在更广泛应用的沸石中尚未实现,在沸石中,通常使用探索性合成来发现新材料。尽管已经提出了数百万种假设的沸石结构,但对其合成机制的了解还不够,无法制备任何给定的结构。在这里,我们提出了一种将结构解析与结构预测相结合的方法,并启发了新的超复杂沸石的靶向合成。我们使用电子衍射来识别一系列相关结构,并发现其中的结构“编码”。这使我们能够确定沸石 ZSM-25 的复杂且以前未知的结构(8),它具有所有已知沸石中最大的晶胞体积(91,554 立方 ångströms),并表现出选择性 CO2 吸附。通过扩展我们的方法,我们能够预测该家族中其他越来越复杂但结构相关的沸石成员,并在该家族中合成另外两种更复杂的沸石 PST-20 和 PST-25,其晶胞体积更大(分别为 166,988 和 275,178 立方 ångströms),并且具有相似的选择性吸附特性。这个家族的成员具有相同的对称性,但晶胞膨胀,由迄今为止尚未被认识到的结构原理联系在一起;我们将这些家族成员称为嵌入式等孔沸石结构。