Structure-Property Relationship of Piezoelectric Properties in Zeolitic Imidazolate Frameworks: A Computational Study

Metal-organic frameworks (MOFs) are a class of nanoporous crystalline materials with very high structural tunability. They possess a very low dielectric permittivity epsilon r due to their porosity and hence are favorable for piezoelectric energy harvesting. Even though they have huge potential as piezoelectric materials, a detailed analysis and structure-property relationship of the piezoelectric properties in MOFs are lacking so far. This work focuses on a class of cubic non-centrosymmetric MOFs, namely, zeolitic imidazolate frameworks (ZIFs) to rationalize how the variation of different building blocks of the structure, that is, metal node and linker substituents affect the piezoelectric constants. The piezoelectric tensor for the ZIFs is computed from ab initio theoretical methods. From the calculations, we analyze the different contributions to the final piezoelectric constant d14, namely, the clamped ion (e140 ) and the internal strain (e14 int) contributions and the mechanical properties. For the studied ZIFs, even though e14 (e140 + e14int) is similar for all ZIFs, the resultant piezoelectric coefficient d14 calculated from piezoelectric constant e14 and elastic compliance constant s44 varies significantly among the different structures. It is the largest for CdIF-1 (Cd2+ and -CH3 linker substituent). This is mainly due to the higher elasticity or flexibility of the framework. Interestingly, the magnitude of d14 for CdIF-1 is higher than II-VI inorganic piezoelectrics and of a similar magnitude as the quintessential piezoelectric polymer polyvinylidene fluoride.

Automated summary

This study focuses on the piezoelectric properties of a class of cubic non-centrosymmetric MOFs called zeolitic imidazolate frameworks (ZIFs). Through calculations and analysis of different structures, it was found that CdIF-1 (Cd2+ and -CH3 linker substituent) has the highest piezoelectric coefficient, comparable to that of the quintessential piezoelectric polymer.