Unlocking enhanced photocatalytic power: Donor-acceptor synergy in non-metallic g-CN hollow nanospheres.

Selecting safe, non-toxic, and non-metallic semiconductor materials that facilitate the degradation of pollutants in water stands out as an optimal approach to combat environmental pollution. Herein, graphitic carbon nitride (g-CN)-based hollow nanospheres nonmetallic photocatalyst modified with covalent organic framework materials named TpMA, based on 1, 3, 5-trimethylchloroglucuronide (Tp) and melamine (MA), was successfully synthesized (abbreviated as CNTP). The ordered electron donor-acceptor structure inherent in TpMA contributed to enhancing the transport efficiency of photogenerated carriers in CNTP.

Fabrication of a Covalent Organic Framework-Based Heterojunction via Coupling with ZnAgInS Nanosphere with High Photocatalytic Activity.

Covalent organic frameworks (COFs) exhibit visible-light activity for the degradation of organic pollutants. However, the recombination rates of their photoinduced electron-hole pairs are relatively high, limiting their practical application. In this work, we fabricated a 1,3,5-triformylphloroglucinol (Tp) and -phenylenediamine (Pa-1) (TpPa-1) COF-based heterojunction through coupling the TpPa-1 COF with a ZnAgInS nanosphere via a facile oil bath heating method.

Construction of MOF/COF Hybrids for Boosting Sunlight-Induced Fenton-like Photocatalytic Removal of Organic Pollutants.

In this work, a metal-organic framework (MOF) material of NH-MIL88B was hybridized with TpPa-1-COF through covalent bonding, and the hybrid was subsequently employed for the degradation of Rhodamine B (RhB) and tetracycline (TC) by simulated sunlight-induced Fenton-like exciting HO. The obtained results show that its photocatalytic activity is much better than those of its parent MOF and covalent organic framework (COF). Moreover, it is much higher than that of bare photocatalysis without Fenton-like excitation of HO.

Fabrication of 2D-2D Heterojunction Catalyst with Covalent Organic Framework (COF) and MoS for Highly Efficient Photocatalytic Degradation of Organic Pollutants.

In this work, for the first time, we fabricated a novel covalent organic framework (COF)-based 2D-2D heterojunction composite MoS/COF by a facile hydrothermal method. The results of photocatalytic degradation of TC and RhB under simulated solar light irradiation showed that the as-prepared composite exhibited outstanding catalytic efficiency compared with pristine COFs and MoS. The significantly enhanced catalytic efficiency can be ascribed to the formation of 2D-2D heterojunction with a well-matched band position between COF and MoS, which can effectively restrain the recombination of charge carriers and increase the light absorption as well as the specific surface area.

Fabrication of Hierarchical CoS@ZnAgInS Heterostructured Cages for Highly Efficient Photocatalytic Hydrogen Generation and Pollutants Degradation.

In the present study, a hierarchical CoS@ZnAgInS heterostructural cage was developed for the first time which can photocatalytically produce hydrogen and degrade organic pollutants with high efficiency. First, the CoS dodecahedron was synthesized using a metal-organic framework (MOFs) material, ZIF-67, as a precursor, then two kinds of metal sulfide semiconductors were elaborately integrated into a hierarchical hollow heterostructural cage with coupled heterogeneous shells and 2D nanosheet subunits. The artfully designed hollow heterostructural composite exhibited remarkable photocatalytic activity without using any cocatalysts, with a 9395.