无定形固体
介孔材料
材料科学
纳米材料
纳米技术
多孔性
纳米结构
比表面积
金属有机骨架
三元运算
各向异性
结晶学
化学
催化作用
计算机科学
复合材料
有机化学
吸附
物理
量子力学
程序设计语言
作者
Minchao Liu,Cheng Shang,Tiancong Zhao,Hongyue Yu,Yufang Kou,Zirui Lv,Mengmeng Hou,Fan Zhang,Qiaowei Li,Dongyuan Zhao,Xiaomin Li
标识
DOI:10.1038/s41467-023-36832-2
摘要
As an important branch of anisotropic nanohybrids (ANHs) with multiple surfaces and functions, the porous ANHs (p-ANHs) have attracted extensive attentions because of the unique characteristics of high surface area, tunable pore structures and controllable framework compositions, etc. However, due to the large surface-chemistry and lattice mismatches between the crystalline and amorphous porous nanomaterials, the site-specific anisotropic assembly of amorphous subunits on crystalline host is challenging. Here, we report a selective occupation strategy to achieve site-specific anisotropic growth of amorphous mesoporous subunits on crystalline metal-organic framework (MOF). The amorphous polydopamine (mPDA) building blocks can be controllably grown on the {100} (type 1) or {110} (type 2) facets of crystalline ZIF-8 to form the binary super-structured p-ANHs. Based on the secondary epitaxial growth of tertiary MOF building blocks on type 1 and 2 nanostructures, the ternary p-ANHs with controllable compositions and architectures are also rationally synthesized (type 3 and 4). These intricate and unprecedented superstructures provide a good platform for the construction of nanocomposites with multiple functionalities and understanding of the structure-property-function relationships.
科研通智能强力驱动
Strongly Powered by AbleSci AI