化学
金属有机骨架
同位素
Crystal(编程语言)
晶体结构
金属
动力学同位素效应
环境化学
结晶学
放射化学
无机化学
有机化学
氘
物理
吸附
量子力学
计算机科学
程序设计语言
作者
Lixi Chen,Junhao Lu,Xiaoqi Li,Ni Luan,Yiting Song,Shenghai Yang,Mengjia Yuan,Haoming Qin,Hui‐Fang Zhu,Xue Dong,Kai Li,Duo Zhang,Long Chen,Xing Dai,Yanlong Wang,Yaxing Wang,Chao Xu,Zhifang Chai,Shuao Wang
摘要
Synthesizing large metal-organic framework (MOF) single crystals has garnered significant research interest, although it is hindered by the fast nucleation kinetics that gives rise to numerous small nuclei. Given the different chemical origins inherent in various types of MOFs, the development of a general approach to enhancing their crystal sizes presents a formidable challenge. Here, we propose a simple isotopic substitution strategy to promote size growth in MOFs by inhibiting nucleation, resulting in a substantial increase in the crystal volume ranging from 1.7- to 165-fold. Impressively, the crystals prepared under optimized conditions by normal approaches can be further enlarged by the isotope effect, yielding the largest MOF single crystal (2.9 cm × 0.48 cm × 0.23 cm) among the one-pot synthesis method. Detailed in situ characterizations reveal that the isotope effect can retard crystallization kinetics, establish a higher nucleation energy barrier, and consequently generate fewer nuclei that eventually grow larger. Compared with the smaller crystals, the isotope effect-enlarged crystal shows 33% improvement in the X-ray dose rate detection limit. This work enriches the understanding of the isotope effect on regulating the crystallization process and provides inspiration for exploring potential applications of large MOF single crystals.
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