Yan Fang

The emergence of zerovalent atom catalysts has been highly attractive for catalytic science. For many years, scientists have explored the stability of zerovalent atom catalysts and demonstrated their unique properties. Here, we describe an atom catalyst (AC) with atomically dispersed zerovalent molybdenum atoms on graphdiyne (Mo0/GDY) with a high mass content of Mo atoms (up to 7.5 wt %) that was synthesized via a facile and scalable process. The catalyst shows both excellent selectivity and activity in the electrochemical reduction of nitrogen and in the hydrogen evolution reaction in aqueous solutions at room temperature and pressure. It is noted that this catalyst is the first bifunctional AC for highly efficient and selective ammonia and hydrogen generation. The catalytic process of our catalyst is well understood, the structure is defined, and the performance is excellent, providing a solid foundation for the generation and application of the new generation of catalysts.

, and build the important scientific value of new conversion devices. This review covers research on the foundation and application of GDY, such as the controlled preparation of new methods of GDY and GDY-based materials, studies on new mechanisms and properties in chemistry and physics, and the foundation and applications in energy, catalysis, photoelectric and devices.

Abstract A highly active graphdiyne heterojunction with highly efficient photocatalysis is designed and fabricated. This catalyst demonstrates transformative properties on photocatalysis for ammonia synthesis. Such excellent properties are reigned from graphdiyne incorporating Fe site‐specific magnetite resulting in a valence state transition within the catalyst. Our results show the strong advantages of graphdiyne in effectively regulating magnetite activity and coordination environments and also indicate that magnetite can selectively form two different valence tetrahedral coordination Fe and octahedral coordination Fe. The catalysts show remarkable catalytic performance for ammonia synthesis by photocatalysis, indicating transformative photocatalytic activity with an ammonia yield (Y ) of unprecedented level of 1762.35±153.71 μmol h −1 g cat. −1 (the highest Y could reach up to 1916.06 μmol h −1 g cat. −1 ). This work makes full use of the structural and property features of graphdiyne and opens up a new direction for photocatalysis in the field of catalysis.

We report on the synthesis of inorganic fullerene-like molybdenum disulfide (MoS(2)) nanoparticles by pulsed laser ablation (PLA) in water. The final products were characterized by scanning electron microscopy, X-ray diffraction, transmission electron microscopy, and resonance Raman spectroscopy, etc. Cell viability studies show that the as-prepared MoS(2) nanoparticles have good solubility and biocompatibility, which may show a great potential in various biomedical applications. It is shown that the technique of PLA in water also provides a green and convenient method to synthesize novel nanomaterials, especially for biocompatible nanomaterials.

Abstract A freestanding 3D graphdiyne–cobalt nitride (GDY/Co 2 N) with a highly active and selective interface is fabricated for the electrochemical nitrogen reduction reaction (ECNRR). Density function theory calculations reveal that the interface‐bonded GDY contributes an unique p‐electronic character to optimally modify the Co‐N compound surface bonding, which generates as‐observed superior electronic activity for NRR catalysis at the interface region. Experimentally, at atmospheric pressure and room temperature, the electrocatalyst creates a new record of ammonia yield rate (Y ) and Faradaic efficiency (FE) of 219.72 μg h −1 mg cat. −1 and 58.60 %, respectively, in acidic conditions, higher than reported electrocatalysts. Such a catalyst is promising to generate new concepts, new knowledge, and new phenomena in electrocatalytic research, driving rapid development in the field of electrocatalysis.