微型多孔材料
材料科学
超级电容器
制作
金属有机骨架
结晶
纳米技术
碳纤维
化学工程
电容
复合材料
电极
有机化学
物理化学
复合数
化学
替代医学
吸附
病理
工程类
医学
作者
Qian Li,Zhaowei Dai,Jiabin Wu,Wei Liu,Tuo Di,Rui Jiang,Xue Zheng,Weizhe Wang,Xinxin Ji,Pan Li,Zheheng Xu,Xiaopeng Qu,Zhimou Xu,Jun Zhou
标识
DOI:10.1002/aenm.201903750
摘要
Abstract Because of their good performance in diffusion‐limited processes, ordered macro‐microporous single‐crystalline metal‐organic frameworks (MOFs) have potential for use in various fields. However, there are still very few reports of the synthesis of such MOFs. A general synthesis methodology for ordered macro‐microporous single‐crystalline MOFs is highly desired. Here, a novel strategy is reported for synthesizing single‐crystalline ordered macro‐microporous MOFs by monodentate‐ligand‐induced in situ crystallization within a 3D ordered hard template in a double‐solvent system. A space‐confined growth model is proposed to clarify the shaping effect of the template; the role of the monodentate ligand is also analyzed. Moreover, a carbon material derived from the macro‐microporous MOF inherits the ordered interconnected macroporous structure. The improved diffusion and lower resistance, as well as the structural robustness, endow the derivative carbon material with superior rate performance and excellent cycling stability when prepared as electrodes for a supercapacitor. It is anticipated that the method will provide new paths to the synthesis of such macro‐microporous materials for applications in energy‐related fields and beyond.
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