Effect of Transition Metal Substitution on the Flexibility and Thermal Properties of MOF-Based Solid-Solid Phase Change Materials.

A series of azobenzene-loaded metal-organic frameworks were synthesized with the general formula M(BDC)(DABCO)(AB) (M = Zn, Co, Ni, and Cu; BDC = 1,4-benzenedicarboxylate; DABCO = 1,4-diazabicyclo[2.2.2]octane; and AB = azobenzene), herein named ⊃AB. Upon occlusion of AB, each framework undergoes guest-induced breathing, whereby the pores contract around the AB molecules forming a narrow-pore () framework. The loading level of the framework is found to be very sensitive to the synthetic protocol and although the stable loading level is close to ⊃AB, higher loading levels can be achieved for the Zn, Co, and Ni frameworks prior to vacuum treatment, with a maximum composition for the Zn framework of ⊃AB. The degree of pore contraction upon loading is modulated by the inherent flexibility of the metal-carboxylate paddlewheel unit in the framework, with the ⊃AB showing the biggest contraction of 6.2% and the more rigid ⊃AB contracting by only 1.7%. Upon heating, each composite shows a temperature-induced phase transition to an open-pore () framework, and the enthalpy and onset temperatures of the phase transition are affected by the framework flexibility. For all composites, UV irradiation causes → isomerization of the occluded AB molecules. The population of -AB at the photostationary state and the thermal stability of the occluded -AB molecules are also found to correlate with the flexibility of the framework. Over a full heating-cooling cycle between 0 and 200 °C, the energy stored within the metastable -AB molecules is released as heat, with a maximum energy density of 28.9 J g for ⊃AB. These findings suggest that controlled confinement of photoswitches within flexible frameworks is a potential strategy for the development of solid-solid phase change materials for energy storage.