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Ionic Pairs-Engineered Fluorinated Covalent Organic Frameworks Toward Direct Air Capture of CO 2
Ist Teil von
Small (Weinheim an der Bergstrasse, Germany), 2024-05, Vol.20 (36), p.e2401798
Ort / Verlag
Germany: Wiley Blackwell (John Wiley & Sons)
Erscheinungsjahr
2024
Quelle
Wiley Online Library - AutoHoldings Journals
Beschreibungen/Notizen
The covalent organic frameworks (COFs) possessing high crystallinity and capability to capture low-concentration CO
(400 ppm) from air are still underdeveloped. The challenge lies in simultaneously incorporating high-density active sites for CO
insertion and maintaining the ordered structure. Herein, a structure engineering approach is developed to afford an ionic pair-functionalized crystalline and stable fluorinated COF (F-COF) skeleton. The ordered structure of the F-COF is well maintained after the integration of abundant basic fluorinated alcoholate anions, as revealed by synchrotron X-ray scattering experiments. The breakthrough test demonstrates its attractive performance in capturing (400 ppm) CO
from gas mixtures via O─C bond formation, as indicated by the in situ spectroscopy and operando nuclear magnetic resonance spectroscopy using
C-labeled CO
sources. Both theoretical and experimental thermodynamic studies reveal the reaction enthalpy of ≈-40 kJ mol
between CO
and the COF scaffolds. This implies weaker interaction strength compared with state-of-the-art amine-derived sorbents, thus allowing complete CO
release with less energy input. The structure evolution study from synchrotron X-ray scattering and small-angle neutron scattering confirms the well-maintained crystalline patterns after CO
insertion. The as-developed proof-of-concept approach provides guidance on anchoring binding sites for direct air capture (DAC) of CO
in crystalline scaffolds.
Sprache
Englisch
Identifikatoren
ISSN: 1613-6810
eISSN: 1613-6829
DOI: 10.1002/smll.202401798
Titel-ID: cdi_osti_scitechconnect_2345828
Format
–
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