Smart Responsive Azo-Copolymer with Photoliquefaction for Switchable Adhesive Application.

The development and utilization of switchable adhesives are considered to be an essential target to solve the problems of their separation and recycling in some specific service environments, such as the preparation or repair process of electronic devices. Intelligent materials with controllable phase transition are utilized to fabricate switchable adhesives because of the significantly diverse adhesion strengths in different phase states. Photoresponsive azobenzene and its derivatives usually possess different melting temperatures (Tm) or/and glass transition temperatures (Tg) of the cis-trans isomers, which are beneficial to making the photoinduced solid-liquid phase transition for switchable adhesive application possible. Here, a novel three-component azo-copolymer (PNIM-Azo) with fast and reversible photoinduced solid-liquid phase transition has been designed and synthesized. PNIM-Azo possesses reversible bonding/debonding processes, resulting from the different adhesion strengths between trans-configuration PNIM-Azo in the solid state and cis-configuration in the liquid state. Moreover, by incorporating commercialized 2-methoxyethyl acrylate and N-isopropylacrylamide with O and N heteroatoms into the copolymer, the trans-configuration PNIM-Azo possesses the highest adhesion strength (∼11 MPa between two glass substrates) among all of the reported azobenzene-based switchable adhesives, which could be attributed to the increase in the entanglement effect because of the H-bond in the polymer chains formed by introducing heteroatoms. Our synthesized PNIM-Azo copolymer provides an alternative for designing and developing switchable adhesives with high adhesion strength for some electronic production processes.

A facile one-pot preparation of Bi2O2CO3/g-C3N4 composites with enhanced photocatalytic activity.

Bi2O2CO3 modified graphitic carbon nitride (g-C3N4) nanosheets were prepared by a simple one-pot synthetic strategy. In the presence of ammonium nitrate, different mass ratios of bismuth nitrate/melamine were used to fabricate these catalysts, which were characterized by X-ray diffraction (XRD), N2-physisorption, Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV-vis analysis, and photoluminescence (PL). The catalytic properties of composites were evaluated by photodegrading tetracycline hydrochloride (TC) under visible light irradiation. Among these catalysts, Bi2O2CO3(1.5)/g-C3N4 showed the highest catalytic activity, which was more than 16 times greater than the pristine g-C3N4 material. The improved photocatalytic properties of Bi2O2CO3/g-C3N4 may be due to the formation of a heterojunction between Bi2O2CO3 and g-C3N4, leading to the effective separation of photo-induced carriers and the enhanced absorption of visible light. Furthermore, the Bi2O2CO3/g-C3N4 composites had considerable catalytic stability, which was a key element for their potential applications.

Novel p-n junction UiO-66/BiOI photocatalysts with efficient visible-light-induced photocatalytic activity.

Novel visible-light-induced UiO-66/BiOI photocatalysts with a p-n junction structure have been prepared for the first time through a facile hydrothermal method. The prepared photocatalysts were characterized using the powder X-ray diffraction, high resolution transmission electron microscopy, scanning electron microscopy, UV-visible diffuse reflectance spectra, and N2 adsorption-desorption (Brunauer-Emmett-Teller) techniques respectively. The photodegradation performances of UiO-66/BiOI photocatalysts were evaluated by photodegrading salicylic acid under visible-light irradiation. The UiO-66/BiOI composites displayed much higher photocatalytic efficiencies than pure BiOI under visible light. When the content of UiO-66 was 5.2 wt%, the composite (UiO-66/BiOI-2) has the best photocatalytic activity. Most of the salicylic acid molecules can be degraded in 100 min. The degradation rate of UiO-66/BiOI-2 samples is higher than single BiOI and UiO-66. The enhanced photocatalytic performance of UiO-66/BiOI may be ascribed to the formation of p-n heterojunctions between BiOI and UiO-66, which facilitates the transfer and separation of the photogenerated charge carriers. After recycling of the photocatalyst for five times for the photodegradation of salicylic acid, more than 85% of salicylic acid could still be degraded in the fifth cycle, implying that the as-prepared photocatalysts are highly stable.