ABSTRACT
Hydrogen-bonded organic frameworks (HOFs), self-assembled from organic or metalated organic building blocks (also termed as tectons) by hydrogen bonding, π-π stacking, and other intermolecular interactions, have become an emerging class of multifunctional porous materials. So far, a library of HOFs with high porosity has been synthesized based on versatile tectons and supramolecular synthons. Benefiting from the flexibility and reversibility of H-bonds, HOFs feature high structural flexibility, mild synthetic reaction, excellent solution processability, facile healing, easy regeneration, and good recyclability. However, the flexible and reversible nature of H-bonds makes most HOFs suffer from poor structural designability and low framework stability. In this Outlook, we first describe the development and structural features of HOFs and summarize the design principles of HOFs and strategies to enhance their stability. Second, we highlight the state-of-the-art development of HOFs for diverse applications, including gas storage and separation, heterogeneous catalysis, biological applications, sensing, proton conduction, and other applications. Finally, current challenges and future perspectives are discussed.
ABSTRACT
Efficient hydrogen production through water splitting has been the challenging task to be achieved in the present context of energy crisis. Among the various catalysts employed, nitrogen doped Titanium dioxide/Reduced graphene oxide (N-TiO2/RGO) nanocomposite has been established to be a promising photocatalytic material for this purpose. However, nuances of doping nitrogen on TiO2 and the type of nitrogen (pyridinic, pyrrolic and graphitic) stabilized on RGO responsible for facilitating the H2 production has not yet been addressed mechanistically. In the present investigation, an attempt has been made to synthesise N-Titanium dioxide/N-Reduced graphene oxide (NTNG) nanocomposite under ultrasonication followed by hydrothermal treatment. A stainlesssteel ultrasonic bath, of 6.5â¯L tank size (LxBxH) 300â¯×â¯150â¯×â¯150â¯mm, was used for ultrasonic treatments. The transducers located at the bottom of the ultrasonic bath generate a frequency of 40â¯kHz with maximum power of 200â¯W. A mechanism has been proposed including the nuances of formation and the stabilisation of each type of nitrogen on N-RGO as a function of ultrasonication time. The present work supports the stabilization of a given type of nitrogen on RGO through keto enol tautomerism. XPS and FTIR studies have been undertaken to identify the different types of nitrogen doping and the presence of functional groups respectively. XRD, UV-Vis DRS and PL investigations have been made to establish morphological profile and band gap structure of the nanocomposite. It was observed that pyrrolic type nitrogen stabilized on N-RGO augments the efficiency of photocatalytic activity through hydrogen production by water splitting.