4.5 Article

Light-induced Photoswitching of 4-(Phenylazo)benzoic Acid on Au(111)

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CHEMPHYSCHEM
卷 24, 期 17, 页码 -

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.202300160

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azo compounds; molecular switches; photoisomerization; pulse deposition; scanning probe microscopy

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Photochromic molecules can transform between two isomeric forms upon exposure to external stimuli, making them potential photoswitches for molecular electronic devices. Understanding the photoisomerization process on surfaces and its dependence on the local chemical environment is crucial for their efficient use in these applications.
Photochromic molecules can undergo a reversible conversion between two isomeric forms upon exposure to external stimuli such as electromagnetic radiation. A significant physical transformation accompanying the photoisomerization process defines them as photoswitches, with potential applications in various molecular electronic devices. As such, a detailed understanding of the photoisomerization process on surfaces and the influence of the local chemical environment on switching efficiency is essential. Herein, we use scanning tunneling microscopy to observe the photoisomerization of 4-(phenylazo)benzoic acid (PABA) assembled on Au(111) in kinetically constrained metastable states guided by pulse deposition. Photoswitching is observed at low molecular density and is absent in tight-packed islands. Furthermore, switching events were noted in PABA molecules coadsorbed in a host octanethiol monolayer, suggesting an influence of the surrounding chemical environment on photoswitching efficiency.

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