Shan Dai, Longzhang Dong, Yinlin Chen, Jiangnan Li, Justyna Rogacka, Yuhang Yang, Zi Wang, Benjamin J. Moore, Daniel Lee, Yongqiang Cheng, Svemir Rudić, Bogdan Kuchta, Mark D. Frogley, Lucy Saunders, Martin Schröder, S M Yang
The desulfurization of flue gas requires sorbents capable of selective and reversible SO 2 capture. However, top-performing materials operate through either strong binding sites or the use of narrow pores, leading to difficulties in desorption and materials regeneration. Here, we report the efficient capture of trace SO 2 using a robust and scalable aluminum-based metal–organic framework, MIL-120, which shows an exceptional SO 2 uptake of 2.1 mmol g –1 at 2500 ppm and 298 K, coupled with optimal heats of adsorption (19–42 kJ mol –1 ) and fully reversible desorption at room temperature. Direct visualization of adsorbed SO 2 molecules reveals host–guest and guest–guest interactions, collectively affording an SO 2 packing density of 1.92 g cm –3, formally surpassing that of solid SO 2 (1.62 g cm –3 ). Breakthrough experiments demonstrate that MIL-120 exhibits remarkable trace SO 2 capture in the presence of dry or wet NO 2 (another corrosive gas present in flue gas) with a record dynamic selectivity of 124, confirming the potential for MIL-120 to separate SO 2 /NO 2 mixtures. This work sets a new benchmark for sorbent materials for reversible trace SO 2 capture and separation.