渗透
材料科学
气体分离
石墨烯
膜
选择性
化学工程
氧化物
位阻效应
纳米技术
多孔性
多孔介质
纳米
渗透
膜技术
空气分离
氧气
限制
热的
胺气处理
氮气
GSM演进的增强数据速率
作者
Kuang‐Jung Hsu,Marina Micari,Yueqing Shen,Shaoxian Li,Shuqing Song,Kumar Varoon Agrawal
标识
DOI:10.1002/adma.202519645
摘要
Graphene with angstrom-scale, zero-dimensional pores offers a promising platform for gas separations due to its exceptional permeance and potential for molecular sieving. Herein, we demonstrate a dynamic strategy to tune N-functionalized graphene pores, achieving selective oxygen (O2) separation from nitrogen (N2), a particularly challenging separation due to their similar kinetic diameters. We exploit the heterogeneity of functional groups at the pore edge to tune the pore limiting diameter (PLD). By facile thermal annealing, we convert primary amine groups at the pore edge to lattice-incorporated nitrogen. Temperature-dependent extent of conversion allows to tune the steric hindrance from amine-CO2 complex, and therefore, PLD for O2/N2 separation in favor of O2 permeation. The resulting membranes exhibit attractive O2/N2 separation performance, with O2 permeance near 2500 GPU with O2/N2 selectivity above 10, significantly outperforming the state-of-the-art membranes. This is attractive for energy-efficient and modular production of O2 from air and can cut down fuel consumption in natural gas-fired furnaces in the chemical industry by 60%.
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