Oxygen-rich carbon-anchored NH2-MIL series MOFs for room-temperature catalytic adsorption of gaseous formaldehyde and optimization through tuning hybrid composition

Catalytic adsorption is a light-free, energy-independent approach to remediate hazardous gasous compounds, such as formaldehyde (FA), by synergistically combining high adsorption capacity with intrinsic catalytic oxidation activity in the dark at room temperature (DRT). Accordingly, a design principle that couples oxygen-rich activated carbons (C-X: X = A [acid-oxidized] or P [permanganate-oxidized]) and amino functionalized MIL type metal organic frameworks (NH 2 -MIL MOFs) with different metal centers (M-Y: Y = F [Fe], A [Al], or T [Ti]) is implemented to screen composite pairs for synergistic FA conversion under DRT, ambient conditions. The optimal pairing, C-A with M-T, is then formulated as CM-Z, where Z is the C-A/M-T weight ratio (in %). The air purifier (AP) constructed with CM-50 honeycomb filter exhibits superior performance against a wide range of FA concentrations (1–100 ppm). For dry FA (5 ppm), CM-50 demonstrates a clean air delivery rate of 6.92 L min − 1 with sustained mineralization capability (~ 60% CO 2 yield) over five consecutive cycles at DRT. Mechanistically, the enhanced performance arises from an emergent, interface-enabled reaction pathway rather than a simple synergistic effect of adsorption and catalysis. Density functional theory reveals that the Ti containing NH 2 MIL (M-T) stabilizes and activates FA at Ti–O and –NH 2 sites, while the oxygen rich carbon (C-A) facilitates proton transfer across the interface. This cooperative activation is corroborated by the detection of intermediates (e.g., CH 2 O 2 , HCOO⁻, CO 3 2− , H 2 O, and CO 2 ) and by the evolution of surface elemental states in CM-50 during the filtration at DRT. This interface-enabled catalytic adsorption mechanism supports sustained FA conversion and partial mineralization without external energy input. The results position CM-basedcatalytic adsorbents as a viable, energy-independent platform for indoor air quality management.

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Journal
Advanced Composites and Hybrid Materials
Published
2026-06-12
DOI
https://doi.org/10.1007/s42114-026-01881-w
Primary Topic
Metal-Organic Frameworks: Synthesis and Applications
Type
article
Field-Weighted Citation Impact
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article

Oxygen-rich carbon-anchored NH2-MIL series MOFs for room-temperature catalytic adsorption of gaseous formaldehyde and optimization through tuning hybrid composition

Sherif A. Younis, Xueli He, Ki-Hyun Kim, Danil. W. Boukhvalov
Advanced Composites and Hybrid Materials
Metal-Organic Frameworks: Synthesis and Applications
article

Oxygen-rich carbon-anchored NH2-MIL series MOFs for room-temperature catalytic adsorption of gaseous formaldehyde and optimization through tuning hybrid composition

Sherif A. Younis, Xueli He, Ki-Hyun Kim, Danil. W. Boukhvalov
article en

Abstract

Catalytic adsorption is a light-free, energy-independent approach to remediate hazardous gasous compounds, such as formaldehyde (FA), by synergistically combining high adsorption capacity with intrinsic catalytic oxidation activity in the dark at room temperature (DRT). Accordingly, a design principle that couples oxygen-rich activated carbons (C-X: X = A [acid-oxidized] or P [permanganate-oxidized]) and amino functionalized MIL type metal organic frameworks (NH 2 -MIL MOFs) with different metal centers (M-Y: Y = F [Fe], A [Al], or T [Ti]) is implemented to screen composite pairs for synergistic FA conversion under DRT, ambient conditions. The optimal pairing, C-A with M-T, is then formulated as CM-Z, where Z is the C-A/M-T weight ratio (in %). The air purifier (AP) constructed with CM-50 honeycomb filter exhibits superior performance against a wide range of FA concentrations (1–100 ppm). For dry FA (5 ppm), CM-50 demonstrates a clean air delivery rate of 6.92 L min − 1 with sustained mineralization capability (~ 60% CO 2 yield) over five consecutive cycles at DRT. Mechanistically, the enhanced performance arises from an emergent, interface-enabled reaction pathway rather than a simple synergistic effect of adsorption and catalysis. Density functional theory reveals that the Ti containing NH 2 MIL (M-T) stabilizes and activates FA at Ti–O and –NH 2 sites, while the oxygen rich carbon (C-A) facilitates proton transfer across the interface. This cooperative activation is corroborated by the detection of intermediates (e.g., CH 2 O 2 , HCOO⁻, CO 3 2− , H 2 O, and CO 2 ) and by the evolution of surface elemental states in CM-50 during the filtration at DRT. This interface-enabled catalytic adsorption mechanism supports sustained FA conversion and partial mineralization without external energy input. The results position CM-basedcatalytic adsorbents as a viable, energy-independent platform for indoor air quality management.

Advanced Composites and Hybrid Materials
Nanjing Forestry University (CN), Satbayev University (KZ), Hanyang University (KR), Egyptian Petroleum Research Institute (EG), Anyang University (KR)
National Research Foundation of Korea
Openalex Percentile: Top 14%
Metal-Organic Frameworks: Synthesis and Applications
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