Reactivity of Bioinspired Magnesium-Organic Networks under CO2 and O-2 Exposure
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Date
2019-06-30Author
Hurtado Salinas, Daniel Eduardo
Sarasola Iñiguez, Ane
Stel, Bart
Cometto, Fernando P.
Kern, Klaus
Lingenfelder, Magalí Alejandra
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ACS Omega 4(6) : 9850-9859 (2019)
Abstract
Photosynthesis is the model system for energy conversion. It uses CO2 as a starting reactant to convert solar energy into chemical energy, i.e., organic molecules or biomass. The first and rate-determining step of this cycle is the immobilization and activation of CO2, catalyzed by RuBisCO enzyme, the most abundant protein on earth. Here, we propose a strategy to develop novel biomimetic two-dimensional (2D) nanostructures for CO2 adsorption at room temperature by reductionist mimicking of the Mg-carboxylate RuBisCO active site. We present a method to synthesize a 2D surface-supported system based on Mg2+ centers stabilized by a carboxylate environment and track their structural dynamics and reactivity under either CO2 or O-2 exposure at room temperature. The CO2 molecules adsorb temporarily on the Mg2+ centers, producing a charge imbalance that catalyzes a phase transition into a different configuration, whereas O-2 adsorbs on the Mg2+ center, giving rise to a distortion in the metal-organic bonds that eventually leads to the collapse of the structure. The combination of bioinspired synthesis and surface reactivity studies demonstrated here for Mg-based 2D ionic networks holds promise for the development of new catalysts that can work at room temperature.