Mihael Gerkman and Prof. Grace Han in the Department of Chemistry report the first demonstration of redox-induced energy release from molecular solar thermal (MOST) compounds in condensed phases, in collaboration with a team of Prof. Matthew Fuchter at Imperial College London. MOST compounds that utilize light-induced chemical isomerization for harnessing solar photon energy have emerged as an alternative to photovoltaics and artificial photosynthesis, enabling a closed-system solar photon energy storage and controlled release. Despite the discovery of various photoswitch systems that show improved photon energy storage efficiencies, the efficient and complete energy release from such photoswitches has remained a major challenge.
This work describes electrochemically-induced switching of arylazopyrazole-based photoswitches. The switching itself is electrocatalytic, requiring only a substoichiometric amount of charge, and its efficiency is improved by over an order of magnitude in the condensed phase compared to in solution. Moreover, electrochemically-induced switching affords a significantly higher completeness of switching than what could be achieved photochemically, which addresses the critical limitation of various azoheteroarene-based MOST materials. We envision that this work will promote exploration of the use of an electrical trigger for MOST material applications for a wide variety of photoswitches.
Jake L. Greenfield‡, Mihael A. Gerkman‡, Rosina S. L. Gibson, Grace G. D. Han*, and Matthew J. Fuchter* J. Am. Chem. Soc. 2021, 143, 37, 15250–15257. (‡ equal contributions) Publication Date: September 14, 2021.
