Edge electron-rich carbon nitride via π-acceptor frame with high-efficient charge separation for photocatalytic hydrogen evolution and environmental remediation.

Carbon nitride (g-CN) has broad application prospects in photocatalytic hydrogen production, but its photocatalytic efficiency is not ideal because of the rapid recombination of photogenerated electrons and holes. Herein, we developed a green strategy to fabricate hydroxyls and carbon-bridging co-modified g-CN (CCN-OH) through a one-pot copolymerization and hydrothermal treatment. Experiments and density functional theory (DFT) calculations illustrated that carbon substitution of partial bridge nitrogen can improve the degree of electron delocalization to enhance the electron supply capacity of g-CN, and the exsitence of the electron-withdrawing OH group induces electron migration from carbon nitride to hydroxyl group, which further improves the efficiency of photogenerated charge separation.

Nitrobenzene inarched carbon nitride nanotube drives efficient directional carriers separation for superior photocatalytic hydrogen production.

Carbon nitride (g-CN) is aussichtsreich for photocatalytic hydrogen evolution, but its photocatalytic activity is not ideal due to the existence of photogenerated electrons and holes in the form of excitons. Herein, a novel nitrobenzene inarched g-CN nanotube photocatalyst (CN-DNP) was firstly fabricated via a facial copolymerization method. The aromatic ring in nitrobenzene could enhance the conjugation of carbon nitride to promote electron delocalization.

Sulfur/phosphorus doping-mediated morphology transformation of carbon nitride from rods to porous microtubes with superior photocatalytic activity.

Hetero-atoms doping or morphology controlling of carbon nitride (g-CN) can availably regulate its electronic band structure and optimize photocatalytic performance under visible light. Herein, sulful (S), phosphorus (P) co-doped porous carbon nitride microtubes (SPCN) was synthesized by using ammonium dihydrogen phosphate and melamine as precursors, in which ammonium dihydrogen phosphate can not only control the morphology of carbon nitride from nanorods to porous microtubes, but also provide a potential P source for P-doped CN. The prepared SPCN0.

Novel B-N-Co surface bonding states constructed on hollow tubular boron doped g-CN/CoP for enhanced photocatalytic H evolution.

Graphitic carbon nitride (g-CN) is a promising photocatalyst for water hydrogen evolution. Nonetheless, fast recombination of photogenerated electron-hole pairs and the slow kinetics of hydrogen production result in the unsatisfactory efficiency of solar hydrogen production. we address this issue by anchoring the cobalt phosphide (CoP) cocatalyst onto the one-dimensional boron doped g-CN nanotube (B-CNNT) to construct B-N-Co surface bonding states in the B-CNNT/CoP photocatalyst.

Self-assembly of emissive metallocycles with tetraphenylethylene, BODIPY and terpyridine in one system.

Tetraphenylethylene (TPE) related (supra)molecules have been intensively investigated due to their aggregation-induced emission (AIE) effect based on the restriction of intramolecular rotation (RIR). Meanwhile, boron-dipyrromethene (BODIPY) tends to emit intense fluorescence with high quantum yields. Herein, we combined TPE, BODIPY and terpyridine (TPY) into one system to study the emissive behaviour of organic building block as well as a self-assembled metallo-supramolecule.

Gas assisted method synthesis nitrogen-doped carbon quantum dots and Hg (II) sensing.

Nitrogen-doped fluorescent carbon quantum dots (CQDs) was prepared by gas-assisted method using cellulose as precursors under ammonia atmosphere, which not only exhibited excellent photoluminescent properties, but also showed highly selective and sensitive detection of mercury ion. The nitrogen-doped CQDs displayed excitation wavelength dependent fluorescent behavior with outstanding dispersibility. Moreover, they exhibited high tolerance to various external conditions, such as storage time, pH value, and ionic strength.