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Eliminating Fatigue in Surface-Bound Spiropyrans.

Sumit Kumar1,2, Saurabh Soni1,2, Wojciech Danowski1,2

  • 1Zernike Institute for Advanced Materials, Nijenborgh 4, 9747 AG Groningen, The Netherlands.

The Journal of Physical Chemistry. C, Nanomaterials and Interfaces
|November 2, 2019
PubMed
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Researchers developed a method to prevent photochromic compound fatigue on surfaces. Mixed monolayers with hexanethiol enable reversible switching over 100 cycles under dry conditions, crucial for device functionality.

Area of Science:

  • Materials Science
  • Surface Chemistry
  • Photochemistry

Background:

  • Surface-bound spiropyrans suffer from limited reversibility and fatigue due to molecular proximity.
  • Photochromic compounds on surfaces lose functionality rapidly, hindering device applications.

Purpose of the Study:

  • To investigate methods for eliminating the loss of reversibility in surface-bound spiropyrans.
  • To enhance the stability and switching cycles of photochromic compounds on surfaces.

Main Methods:

  • Utilized photoelectron spectroscopy and tunneling current measurements to characterize spiropyran and merocyanine forms.
  • Fabricated self-assembled monolayers (SAMs) of pure spiropyrans and mixed SAMs with hexanethiol.
  • Investigated the effect of relative humidity on the performance of mixed SAMs.

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Main Results:

  • Pure spiropyran SAMs degraded rapidly.
  • Mixed SAMs with hexanethiol showed reversible switching over 100 cycles under dry conditions.
  • Under humid conditions, mixed SAMs exhibited irreversible switching without degradation.
  • Lack of solvation in dry conditions was identified as key to suppressing degradation and irreversibility.

Conclusions:

  • Mixed monolayers effectively suppress fatigue and irreversibility in surface-bound photochromic compounds.
  • Environmental factors, particularly humidity, significantly influence the switching behavior and stability.
  • This approach enables the extraction of device-relevant functionality from surface-bound switches.