Unperturbed π‐Methyl Electrostatic Interactions Enable Efficient Toluene Adsorption on Graphdiyne Under High Humidity

S Shaowen Zhang Z Ze Xu (Department of Physics) S Siyi Song H Haitao Shi (Institute of Environmental and Applied Chemistry College of Chemistry Central China Normal University Wuhan People's Republic of China) B Biluan Zhang X Xiaofeng Qiu B Baojian Zhang E En Liang (Institute of Environmental and Applied Chemistry College of Chemistry Central China Normal University Wuhan People's Republic of China) M Meiqi Yao (Institute of Environmental and Applied Chemistry College of Chemistry Central China Normal University Wuhan People's Republic of China) L Lei Gui (Institute of Environmental and Applied Chemistry College of Chemistry Central China Normal University Wuhan People's Republic of China) J Ji Yang (New Cornerstone Science Laboratory, State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, and National & Local Joint Engineering Research Center of Preparation Technology of Nanomaterials, College of Chemistry and Chemical Engineering) J Junbo Li Y Yanbing Guo (Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, Ministry of Education, College of Chemistry)

Abstract

ABSTRACT The efficiency of volatile organic compounds (VOCs) abatement in humid industrial streams is critically hindered by competitive moisture adsorption and the structural vulnerability of conventional adsorbents. Here, we show that a highly hydrophobic graphdiyne (GDY) framework provides a robust platform for sustained VOC capture under highly humid conditions. Dynamic breakthrough measurements demonstrate that GDY maintains > 98% of its toluene uptake (102.5 mg/g) at 50% relative humidity (RH) with excellent cyclic stability, whereas conventional carbonaceous adsorbents usually undergo severe capacity loss. Combined experimental characterization and molecular simulations reveal that the sp‐C linkages induce electron density redistribution, fostering π‐methyl electrostatic interactions that stabilize toluene adsorption. Meanwhile, the highly delocalized π‐electron structure of sp‐hybridized carbon suppresses dipole interactions with water molecules and hinders hydrogen bond formation at the adsorbent surface, thereby suppressing competitive adsorption of water. Our study sheds light on the origin of GDY's moisture tolerance and offers practical guidance for the rational design of hydrophobic adsorbents for industrial gas purification.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 24, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

S

Shaowen Zhang

Z

Ze Xu

Department of Physics

S

Siyi Song

H

Haitao Shi

Institute of Environmental and Applied Chemistry College of Chemistry Central China Normal University Wuhan People's Republic of China

B

Biluan Zhang

X

Xiaofeng Qiu

B

Baojian Zhang

E

En Liang

Institute of Environmental and Applied Chemistry College of Chemistry Central China Normal University Wuhan People's Republic of China

M

Meiqi Yao

Institute of Environmental and Applied Chemistry College of Chemistry Central China Normal University Wuhan People's Republic of China

L

Lei Gui

Institute of Environmental and Applied Chemistry College of Chemistry Central China Normal University Wuhan People's Republic of China

J

Ji Yang

New Cornerstone Science Laboratory, State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, and National & Local Joint Engineering Research Center of Preparation Technology of Nanomaterials, College of Chemistry and Chemical Engineering

J

Junbo Li

Y

Yanbing Guo

Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, Ministry of Education, College of Chemistry