Tailoring the structure and properties of graphene fibers is an important step toward practical applications. Here, we report macroscopic, long graphene ribbons formed by combining electrostatic interaction and shear stress during the wet-spinning process. The graphene ribbons are flexible and can be woven into complex structures, and the ribbon morphology can be tailored by controlling the orientation of wrinkles to obtain elasticity within a modest strain. We demonstrate several potential applications of pure or Pt-graphene hybrid ribbons as elastic strain sensors, counter electrodes for dye-sensitized fiber solar cells with cell efficiencies reaching 4.69% under standard illumination and 6.41% with a back reflector, and woven fabric supercapacitor electrodes. Our method can directly fabricate meter-long graphene ribbons with controlled structure and high performance as both energy conversion and energy storage materials.

Sonodynamic therapy (SDT) has emerged as a promising therapeutic modality for anticancer treatments and is becoming a cutting-edge interdisciplinary research field. This review starts with the latest developments of SDT and provides a brief comprehensive discussion on ultrasonic cavitation, sonodynamic effect, and sonosensitizers in order to popularize the basic principles and probable mechanisms of SDT. Then the recent progress of MOF-based sonosensitizers is overviewed, and the preparation methods and properties (e.g., morphology, structure, and size) of products are presented in a fundamental perspective. More importantly, many deep observations and understanding toward MOF-assisted SDT strategies were described in anticancer applications, aiming to highlight the advantages and improvements of MOF-augmented SDT and synergistic therapies. Last but not least, the review also pointed out the probable challenges and technological potential of MOF-assisted SDT for the future advance. In all, the discussions and summaries of MOF-based sonosensitizers and SDT strategies will promote the fast development of anticancer nanodrugs and biotechnologies.

A new poly­(vinyl alcohol) (PVA) sponge-supported nanocatalysis platform on a continuous-flow microfluidic multireactor device was constructed for high-efficiency and high-reusability catalytic degradation of environmental pollutants. PVA sponge-supported metal nanoparticle catalysts (MNPs/PVA) were prepared by a simple improved impregnation self-assembly method, without any complicated surface modification. The MNPs/PVA catalysts were further integrated on a multireactor microfluidic device to form a continuous flow (CF) reactor platform (MNPs/PVA/chip) for simultaneous catalytic degradation of pollutants with two different nanocatalysts. After condition and catalyst optimizations, the catalytic activities of AuNPs/PVA and CoNPs/PVA were evaluated on this continuous flow microfluidic multireactor platform, by using p-nitrophenol (4-NP) as a model organic pollutant. Both catalysts exhibited outstanding catalytic efficiency (e.g., 100% for fresh catalysts), and the strong interactions between MNPs and PVA ensured high reusability (e.g., >20 cycles). After 20 cycles of catalysis, the optimal catalyst AuNPs/PVA still maintained a high catalytic efficiency of 97.6%. Compared to AuNPs/PVA-5, the cost-effective CoNPs/PVA catalyst exhibited similar catalytic performance within the first 10 cycles, while AuNPs/PVA showed better stability for long-term use. Hence, this continuous flow catalytic platform that combines the advantages of porous material-supported nanocatalysts with microfluidic devices has tremendous potential for various cost-effective environmental research and practical applications.

Luminol is a classic electrochemiluminescence (ECL) luminophore. The luminol−O 2 ECL system suffers from a problem, that is, the conversion rate of dissolved O 2 into reactive oxygen species (ROS) is low. In this work, we used high-intensity focused ultrasound (HIFU) pretreatment combined with Ti 3 C 2 −TiO 2 to construct a highly sensitive luminol−O 2 ECL system for the specific detection of polynucleotide kinase (PNK) first. On the one hand, HIFU generated ROS in situ as a coreactant via the cavitation effect to boost the luminol emission. On the other hand, Ti 3 C 2 −TiO 2 was prepared in situ via Ti 3 C 2 as a reducing agent, and it can aggregate and catalyze ROS generated in situ by HIFU. Moreover, the Ti on the Ti 3 C 2 −TiO 2 surface could bind to phosphate groups through chelation, thereby realizing highly specific detection of PNK. The sensor has a linear relationship range of 1.0 × 10 −5 to 10.0 U mL −1 , and the limit of detection is 1.48 × 10 −7 U mL −1 , which is superior to most existing methods. The sensor performance in HeLa cell lysate was measured with a satisfactory result. The designed ECL biosensor has potential applications in biological analysis and clinical diagnosis. KEYWORDS: electrochemiluminescence, high-intensity focused ultrasound, Ti 3 C 2 −TiO 2 , luminol−O 2 , polynucleotide kinase

Herein, we report a new approach to methylenation of alcohols using N-methyl amide as a sustainable methylene reagent; the N-methyl delivers the methylene group. This new reagent is easily prepared and stable to both air and moisture. Furthermore, the final byproduct of this methylene reagent can be recycled in excellent yields and then reused in methylenation reactions upon treating with CH3I.