期刊
SCIENCE ADVANCES
卷 5, 期 11, 页码 -出版社
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.aax9171
关键词
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资金
- Science Foundation Ireland [13/RP/B2549, 16/IA/4624]
- National Science Foundation [DMR-1607989]
- Major Research Instrumentation Program [CHE1531590]
- XSEDE [TG-DMR090028]
- American Chemical Society Petroleum Research Fund grant [ACS PRF 56673-ND6]
CO2 accumulation in confined spaces represents an increasing environmental and health problem. Trace CO2 capture remains an unmet challenge because human health risks can occur at 1000 parts per million (ppm), a level that challenges current generations of chemisorbents (high energy footprint and slow kinetics) and physisorbents (poor selectivity for CO2, especially versus water vapor, and/or poor hydrolytic stability). Here, dynamic breakthrough gas experiments conducted upon the ultramicroporous material SIFSIX-18-Ni-beta reveal trace (1000 to 10,000 ppm) CO2 removal from humid air. We attribute the performance of SIFSIX-18-Ni-beta to two factors that are usually mutually exclusive: a new type of strong CO2 binding site and hydrophobicity similar to ZIF-8. SIFSIX-18-Ni-beta also offers fast sorption kinetics to enable selective capture of CO2 over both N-2 (S-CN) and H2O (S-CW), making it prototypal for a previously unknown class of physisorbents that exhibit effective trace CO2 capture under both dry and humid conditions.
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