Reversible friction regulation is of long-standing great interest in the fields of both industry and scientific research, so some materials and theories have been developed aiming to solve this problem. Light-sensitive materials are promising because of the easy controllable switching of the properties and structures. Here, a reversible light-controlled macrolubrication was realized by regulating the performance of nanoscale light-sensitive molecules adsorbed on contact surfaces. In this work, symmetric diarylethene and asymmetric diarylethene had been designed and synthesized as functional materials. The friction forces were found to be obviously increased upon exposure to ultraviolet light and decayed to the initial value under visible light. In addition, the friction coefficient changed alternately with ultraviolet and visible illumination. According to the results of experiments and simulation of material properties, the behavior was suggested to be attributed to the difference in shear stiffness of the nanoscale diarylethene molecule adsorption layer triggered by two wavelength lights. This work not only provides a new lubrication regulation technology but also develops intelligent engineering materials.

A new fluorescent chemosensor based on a diarylethene was designed and synthesized for sequential recognition of Fe3+ and cysteine.

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Nowadays, reversible friction regulation has become the focus of scientists in terms of the flexible regulatory structure of photosensitive materials and theories since this facilitates rapid development in this field. Meanwhile, as an external stimulus, light possesses great potential and advantages in spatiotemporal control and remote triggering. In this work, we demonstrated two photo-isomerized organic molecular layers, tetra-carboxylic azobenzene (NN4A) and dicarboxylic azobenzene (NN2A), which were selected to construct template networks on the surface of the highly oriented pyrolytic graphite (HOPG) to study the friction properties, corresponding to the arrangement structure of self-assembled layers under light regulation. First of all, the morphology of the self-assembled layers were characterized by a scanning tunneling microscope (STM), then the nanotribological properties of the template networks were measured by atomic force microscope (AFM). Their friction coefficients are respectively changed by about 0.6 and 2.3 times under light control. The density functional theory (DFT) method was used to calculate the relationship between the force intensity and the friction characteristics of the self-assembled systems under light regulation. Herein, the use of external light stimulus plays a significant role in regulating the friction properties of the interface of the nanometer, hopefully serving as a fundamental basis for further light-controlling research for the future fabrication of advanced on-surface devices.

A diarylethene bearing a triazole-linked rhodamine B unit was synthesized. Its fluorescent emission was significantly enhanced in the presence of protons or Cu due to transformation from the pirocyclic form to open-ring form. The fluorescence was quenched sequentially upon irradiation with 297 nm light based on the intramolecular fluorescence resonance energy transfer mechanism. In an acetonitrile: water binary solvent (1: 1 v/v), the compound showed significant fluorescent enhancement for Cu compared with a wide range of tested metal ions with a fast response and a limit of detection of 2.86 × 10 mol L . Using Cu and UV light as the chemical inputs, and fluorescence intensity at 597 nm as the output, a logic gate was developed at the molecular level. Moreover, the compound can be used with a high accuracy to detect Cu in a natural water sample.