Baxter Samuel J, Schneemann Andreas, Ready Austin D, Wijeratne Pavithra, Wilkinson Angus P, Burtch Nicholas C
Sandia National Laboratory , Livermore , California 94550 , United States.
J Am Chem Soc. 2019 Aug 14;141(32):12849-12854. doi: 10.1021/jacs.9b06109. Epub 2019 Jul 31.
Several metal-organic frameworks are known to display negative thermal expansion (NTE). However, unlike traditional NTE material classes, there have been no reports where the thermal expansion of a MOF has been tuned continuously from negative to positive through the formation of single-phase solid solutions. In the system Zn-DMOF-TM, Zn[(bdc)(TM-bdabco)][dabco], the introduction of increasing amounts of TM-bdc, with four methyl groups decorating the benzene dicarboxylate linker, leads to a smooth transition from negative to positive thermal expansion in the - plane of this tetragonal material. The temperature at which zero thermal expansion occurs evolves from ∼186 K for the Zn-DMOF parent structure ( = 0) to ∼325 K for Zn-DMOF-TM ( = 1.0). The formation of mixed linker solid solutions is likely a general strategy for the control of thermal expansion in MOFs.
已知几种金属有机框架显示出负热膨胀(NTE)。然而,与传统的NTE材料类别不同,尚无报道表明通过形成单相固溶体,金属有机框架(MOF)的热膨胀能从负向连续调节到正向。在Zn-DMOF-TM体系,即Zn[(bdc)(TM-bdabco)][dabco]中,引入越来越多带有四个甲基修饰苯二甲酸酯连接体的TM-bdc,会导致这种四方材料在其平面内从负热膨胀向正热膨胀平稳转变。发生零热膨胀的温度从Zn-DMOF母体结构( = 0)时的约186 K演变为Zn-DMOF-TM( = 1.0)时的约325 K。混合连接体固溶体的形成可能是控制MOF热膨胀的通用策略。