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In an NMR sample, precise measurement of the absolute absorption frequencies of nuclei is difficult. A standard internal reference compound is added, and the frequency difference between the reference signal and sample signals is measured.
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Dynamic Imaging of Solvent Exchange-Induced Interlayer Shifting in Single Two-Dimensional Covalent Organic

Xiaojuan Li1, Qiongyao Ning2, Jiaqi Yao2

  • 1School of Materials and Chemistry, Southwest University of Science and Technology, Mianyang 621010, P. R. China.

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|July 24, 2025
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Researchers visualized solvent exchange-induced interlayer shifting in single 2D covalent organic frameworks (COFs). This dynamic imaging reveals particle heterogeneity and solvent effects, advancing understanding of COF properties.

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Chemical Engineering

Background:

  • Interlayer shifting in 2D covalent organic frameworks (COFs) significantly impacts their sorption and catalytic performance.
  • Existing analytical methods provide static, averaged data from bulk samples, limiting insight into dynamic interlayer processes in individual COFs.

Purpose of the Study:

  • To develop and apply a real-time imaging technique for observing solvent exchange-induced interlayer shifting in single 2D COFs.
  • To investigate the dynamics, heterogeneity, and influencing factors of interlayer shifting in response to solvent exchange.

Main Methods:

  • Utilized in situ dark-field optical microscopy (DFM) for real-time dynamic imaging of individual 2D COFs.
  • Employed grayscale intensity analysis of DFM images to quantify interlayer shifting and pore size changes.
  • Performed theoretical simulations to elucidate the governing factors and thermodynamic pathways of interlayer shifting.

Main Results:

  • Successfully visualized solvent exchange-induced interlayer shifting in triphenylbenzene (TPB)-based COFs.
  • Observed an increase in pore size (from quasi-AB to AA stacking) facilitating guest molecule accommodation and increased scattering intensity.
  • Demonstrated significant particle-to-particle heterogeneity in shifting dynamics, influenced by solvent viscosity and interlayer interaction strength.

Conclusions:

  • The developed DFM imaging methodology enables direct observation of dynamic interlayer shifting in single 2D COFs.
  • Solvent exchange triggers interlayer shifting, altering pore size and impacting COF functionality.
  • Theoretical simulations confirm that stacking energies and thermodynamic preferences govern the shifting process during solvent exchange.