Molecular Crystal Sponge for Extraordinary NH 3 Capture

化学 海绵 氢键 分子 羧酸 Crystal(编程语言) 晶体工程 晶体结构 结晶学 类金刚石 衍射 无机化学 蓝图 单晶 X射线晶体学 胺气处理 立体化学 粉末衍射
作者
Xiangyu Gao,Yijin Wang,Wei Chen,Dong Fan,Pengfu Gao,Yunbo Bi,Xiyu Song,Chen Wang,Yuehua Chen,Guillaume Maurin,Dongyuan Zhao,Wei Gong,Banglin Chen,Peng Li
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:148 (20): 20951-20958 被引量:1
标识
DOI:10.1021/jacs.6c04962
摘要

Ammonia is a chemical commodity in high demand that is produced primarily via the Haber–Bosch process. The low equilibrium single-pass conversion of this over 100-year-old process necessitates the refrigeration condensation removal of ammonia to increase the overall hydrogen yield, which has consumed a massive amount of energy. Developing highly efficient ammonia adsorbents to replace the condensation process is the key to realizing sustainable ammonia synthesis. Here, we report a soft hydrogen-bonded molecular crystal built solely from a very simple, easily available, and economical molecule of benzene-1,2,4,5-tetracarboxylic acid. This material exhibits an unusual sponge-like stoichiometric sorption behavior to capture ammonia with extraordinary performances with respect to low concentration uptake capacity (15.1 mmol g –1 at 10 mbar and 298 K), long-term stability, and industrial practicability, outperforming those of reported materials for this purpose. Breakthrough experiments confirm the excellence of this material for recovering captured NH 3 with ultrahigh purity (≥99.9998%) under both dry and wet conditions. Detailed single-crystal and in situ powder X-ray diffraction (PXRD) analyses, coupled with modeling, unequivocally decipher the charge-assisted hydrogen bonding between ammonia and carboxylic acid moieties in driving stepwise pore expansion. This work thus provides a conceptual blueprint of engineering soft molecular crystals for driving selective ammonia capture and energy-efficient ammonia production.
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