Soon Hyeong So, Sunwoo Kim, Minsu Kim, Donghyun Kim, Donghyun Kim, Taehwan Kim, Kiwon Eum, Yun Ho Kim, Junghwan Kim, Dae Woo Kim, Dae Woo Kim
We report the application of mixed-matrix membranes for high-temperature hydrogen separation. To enhance hydrogen selectivity, graphene nanoribbons (GNRs) were incorporated into ZIF-8 fillers, forming a physically confined structure conducive to hydrogen transport. The metal-organic framework (MOF)/GNR filler embedded into a polyimide (PI) matrix yielded a much higher H 2 permeability (298 Barrer, +40%) and H 2 /N 2 selectivity (15, +25%) than the neat PI membrane. In particular, the as-prepared asymmetric membrane achieved a H 2 permeance of 212 ± 45 Gas Permeation Unit (GPU) and H 2 /N 2 selectivity of 19 ± 2 at 35°C. Remarkably, at 300°C, the H 2 permeance rose to 775 ± 139 GPU while maintaining a H 2 /N 2 selectivity of 13 ± 1, outperforming polymer-based membranes. A techno-economic analysis of an NH 3 cracking process demonstrated that this high permeance reduces membrane area requirements by 68.2% and lowers H 2 separation costs by 35.1% compared with operation at 35°C, leading to a 9.8% reduction in the levelized cost of hydrogen.