Boosting C2H6/C2H4 separation via the precise electrostatic modulation of synthetic 1D channel at atomic level

• Published in: Nano research 2024-11, Vol.17 (11), p.10083-10087
• Main Authors: Ainiwaner, Salamanti, Huang, Hengcong, Zheng, Jia-Jia, Li, Fengting, Yang, Xue-Tong, Guo, Yang-Yang, Yuan, Fangli, Yao, Ming-Shui, Gu, Yifan
• Format: Article
• Language: English
• Subjects: Atomic/Molecular Structure and Spectra; Biomedicine; Biotechnology; Chemical separation; Chemistry and Materials Science; Condensed Matter Physics; Electrostatic properties; Ethane; Materials Science; Metal-organic frameworks; Mixtures; Modulation; Nanotechnology; Porous materials; Research Article; Sorption; Surface charge
• ISSN: 1998-0124; 1998-0000
• DOI: 10.1007/s12274-024-6883-z

The regulation of gas sorption via simple pore modification is crucial to molecular recognition and chemical separation. Herein, a rational pore surface electrostatic modulation in synthetic one dimensioned (1-D) channel is demonstrated to boost ethane/ethylene (C 2 H 6 /C 2 H 4 ) selectivity for one-step extraction of C 2 H 4 from C 2 H 6 /C 2 H 4 mixtures. Through the precise modulation of the surface charge arrangement with negatively charged moieties in the 1-D channel of a metal—organic framework (MOF), enhanced C 2 H 6 —host framework and decreased C 2 H 4 —host framework electrostatic interactions were obtained, which resulted in an obvious improvement in adsorption selectivity. Furthermore, the breakthrough separation performance rendered the obtained MOF an efficient adsorbent for C 2 H 4 purification from C 2 H 6 /C 2 H 4 mixture. The combined detail theoretical studies prove that the gas sorption selectivity is remarkably sensitive to framework electrostatic change even in the case of pore surface modification at the atomic level. These results are of fundamental importance to the design of porous materials for challenging separation tasks.