動的硫酸グアニジニウム塩による負圧屈曲を伴う選択的二酸化炭素吸着

Hydrogen bonds' flexible distances and moderate strength entitle compounds to dynamic properties under external stimuli. Here we report multiple phase transitions and counter-intuitive CO₂ adsorption behavior of dynamic guanidinium sulfate (GS) salt assembled via hydrogen-bonds. Exploration based on the energy landscape generated by crystal structure prediction (CSP) reveals three porous GS phases with stability of α > β > γ and the inverse order of porosity, agreeing with experimental results. Transformations among polymorphs via heating or compressing involve ion rearrangement. Adsorption isotherms of β-GS indicate that CO₂ firstly enters the isolated cavities at a low gating pressure, and further increasing CO₂ pressure leads to the continuous gas uptake but reduced pressure at a critical point and thus an unexpected negative pressure inflexion (NPI), followed by the final adsorption saturation. Theoretical calculations demonstrate that the NPI behavior stemmed from the GS structural transition from β to more porous γ-phase, with the γ-GS phase becoming more energy-favorable as CO₂ uptake increases. Specific supramolecular interactions ensure CO₂ selectivity and easy regeneration. With a CO₂ uptake of 4.2 mmol g^-1 (273 K, 100 kPa), GS salt exhibits great promise for CO₂ capture and transport, demonstrating the potential of simple hydrogen-bonded salts as adaptive materials.