四方晶系
结晶学
晶体生长
形态学(生物学)
化学
双锥
合理设计
各向异性
Crystal(编程语言)
羧酸盐
材料科学
各向同性
立体化学
水热合成
五角双锥分子几何
晶体结构
钙
吸附
单晶
晶体工程
纳米技术
摩尔比
纵横比(航空)
微观结构
热液循环
微型多孔材料
作者
Junya Arashima,Tetsuya Yamada,Haruka Yoshikawa,Hiroh Miyagawa,Kunio Yubuta,Fumitaka Hayashi,Takeshi Hagio,Hideki Tanaka,Katsuya Teshima
标识
DOI:10.1021/acs.cgd.6c00035
摘要
The morphological control of crystals is a critical design strategy for maximizing the functional performance of metal–organic frameworks (MOFs). Herein, we focus on modulating the crystal growth of a calcium squarate (Ca-squarate) MOF, chemically formulated as Ca(C 4 O 4 )· x H 2 O─a promising candidate for CO 2 capture. This MOF typically crystallizes in a needle-like morphology (aspect ratio (width/length) range: 0.1–0.3) due to preferential growth along the c -axis of its tetragonal lattice; however, effective strategies to control its morphology are lacking. We report a novel approach to systematically tune its morphology using carboxylate additives. We demonstrate that α-hydroxy carboxylates specifically induced a morphological transition from an anisotropic needle-like form to a more isotropic cubic-like one─a truncated tetragonal bipyramidal crystal growth. With the addition of α-hydroxy carboxylates, the average aspect ratio significantly increased to a maximum of 0.73. Combined experimental and theoretical analyses revealed that this morphological evolution was driven by a “molecular mimicry” mechanism, where the additive mimicked the coordination geometry of the squarate ligand. This mimicry led to a site-selective competitive adsorption on the (001) and high-index facets, effectively suppressing the intrinsic anisotropic growth. These findings provide new guidelines for the rational design of MOF morphologies to enhance material properties.
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