化学
物理吸附
沸石
膜
选择性
纳米孔
气体分离
分离(统计)
化学工程
纳米技术
工作(物理)
分子筛
渗透
原子轨道
膜技术
化学物理
半透膜
分子
分离法
机制(生物学)
磁导率
作者
Xiaoming Yu,Tongwen Yu,Minghui Chu,Kun Li,Yihua Cai,Ming Xue,Haijiao Xie,Weishen Yang
摘要
A single atom, with maximized atomic utilization and a tailored electronic structure, serves as a promising selective site for achieving ultrahigh selectivity in separation membranes. However, single-atom synthesis within membrane pores with the required chemical specificity for separation remains challenging. Here, we demonstrate single-atom gas separation using Ni single atoms confined in the 10-membered ring channels of (h0h)-oriented MFI zeolite membranes, which serve as intrinsic ultraselective sites for CO 2 . At an ultralow Ni loading of 0.037 wt %, the membrane achieves an ultrahigh H 2 /CO 2 separation factor of 596, along with excellent H 2 permeability of 1924 Barrer, while maintaining stable operation for over 200 h. This performance compares favorably with that of state-of-the-art membranes. Mechanistic studies reveal that hybridization of Ni–O orbitals preferentially interacts with CO 2, in contrast to the weak physisorption of H 2 . This work establishes an atomic-level recognition mechanism in nanoporous architectures and offers new design principles for energy-critical gas separations.
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