TY - JOUR
T1 - Molecular Crystal Sponge for Extraordinary NH3 Capture
AU - Gao, Xiangyu
AU - Wang, Yijin
AU - Chen, Wei
AU - Fan, Dong
AU - Gao, Pengfu
AU - Bi, Yunbo
AU - Song, Xiyu
AU - Wang, Chen
AU - Chen, Yongwei
AU - Maurin, Guillaume
AU - Zhao, Dongyuan
AU - Gong, Wei
AU - Chen, Banglin
AU - Li, Peng
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/5/27
Y1 - 2026/5/27
N2 - 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 NH3 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.
AB - 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 NH3 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.
UR - https://www.scopus.com/pages/publications/105040553506
U2 - 10.1021/jacs.6c04962
DO - 10.1021/jacs.6c04962
M3 - 文章
C2 - 42118570
AN - SCOPUS:105040553506
SN - 0002-7863
VL - 148
SP - 20951
EP - 20958
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 20
ER -