Mimicking human skin's functions to develop electronic skins has inspired tremendous efforts in design and synthesis of novel soft materials with simplified fabrication methods. However, it still remains a great challenge to develop electronically conductive materials that are both stretchable and self‐healable. Here it is demonstrated that a ternary polymer composite comprised of polyaniline, polyacrylic acid, and phytic acid can exhibit high stretchability (≈500%) and excellent self‐healing properties. The polymer composite with optimized composition shows an electrical conductivity of 0.12 S cm−1. On rupture, both electrical and mechanical properties can be restored with ≈99% efficiency in a 24 h period, which is enabled by the dynamic hydrogen bonding and electrostatic interactions. It is further shown that this composite is both strain and pressure sensitive, and therefore can be used for fabricating strain and pressure sensors to detect a variety of mechanical deformations with ultrahigh sensitivity. The sensitivity and sensing range are the highest among all of the reported self‐healable piezoresistive pressure sensors and even surpass most flexible mechanical sensors. Notably, this composite is prepared via a solution casting process, which potentially allows for large‐area, low‐cost fabrication electronic skins.
Metal‐free polymer photocatalysts have shown great promise for photocatalytic H2O2 production via two‐electron reduction of molecular O2. The other half‐reaction, which is the two‐electron oxidation of water, still remains elusive toward H2O2 production. However, enabling this water oxidation pathway is critically important to improve the yield and maximize atom utilization efficiency. It is shown that introducing acetylene (CC) or diacetylene (CCCC) moieties into covalent triazine frameworks (CTFs) can remarkably promote photocatalytic H2O2 production. This enhancement is inherent to the incorporated carbon–carbon triple bonds which are essential in modulating the electronic structures of CTFs and suppressing charge recombinations. Furthermore, the acetylene and diacetylene moieties can significantly reduce the energy associated with OH* formation and thus enable a new two‐electron oxidation pathway toward H2O2 production. The study unveils an important reaction pathway toward photocatalytic H2O2 production, reflecting that precise control over the chemical structures of polymer photocatalysts is vital to achieve efficient solar‐to‐chemical energy conversion.
Converting solar energy into storable and transportable chemical fuels using artificial photosynthetic systems can provide an alternative route to the current unsustainable use of fossil fuels, addressing the worldwide energy crisis and environmental issues. Recently, semiconducting polymers have emerged as a very promising class of photocatalysts for water splitting as their electronic and structural properties can be conveniently controlled and systematically designed at a molecular level. Among the various polymer photocatalysts that are reported so far, 2D polymer nanosheets are particularly interesting and gaining more attention. The 2D planar structure offers unique features such as high surface area, abundant surface active sites, efficient charge separation, and facile formation of heterostructures. The design and synthesis of 2D polymer nanosheets have greatly advanced the research in photocatalytic overall water splitting. Here, recent advances in developing photocatalysts based on 2D polymer nanosheets for photocatalytic overall water splitting are highlighted. Specifically, the existing approaches to tune their electronic structures and surface active sites for photocatalysis are discussed. Future opportunities and challenges for developing 2D polymers for photocatalytic overall water splitting are also included.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.