Ti3 C2 -modified g-C3 N4 /MoSe2 S-Scheme Heterojunction with Full-Spectrum Response for CO2 Photoreduction to CO and CH4.

Energy shortage and global warming caused by the extensive use of fossil fuels are urgent problems to be solved at present. Photoreduction of CO2 is considered to be a feasible solution. The ternary composite catalyst g-C3 N4 /Ti3 C2 /MoSe2 was synthesized by hydrothermal method, and its physical and chemical properties were studied by an array of characterization and tests. In addition, the photocatalytic performance of this series of catalysts under full spectrum irradiation was also tested. It is found that the CTM-5 sample has the best photocatalytic activity, and the yields of CO and CH4 are 29.87 and 17.94 µmol g-1 h-1 , respectively. This can be ascribed to the favorable optical absorption performance of the composite catalyst in the full spectrum and the establishment of S-scheme charge transfer channel. The formation of heterojunctions can effectively promote charge transfer. The addition of Ti3 C2 materials provides plentiful active sites for CO2 reaction, and its superior electrical conductivity is also favorable for the migration of photogenerated electrons.

An Integrated Plasma-Photocatalytic System for Upcycling of Polyolefin Plastics.

Nondegradable polyolefin plastics, which account for >60 % of total plastic waste, trigger severe global concerns and thus demand effective management technologies. However, owing to the chemical inertness of non-polar C-C backbones in the polyolefin structure, efficient upcycling of polyolefin plastics under ambient conditions remains a great challenge. This study introduces an integrated plasma-photocatalytic technology, coupling plasma treatment with solar-driven reforming under mild conditions, for the efficient upcycling of polyolefin plastics into value-added hydrogen and gaseous fuels. The first plasma step grafts oxygenated groups, such as -OH, O-C=O, and C=O, onto the polyolefin chains, which leads to the formation of a polar and hydrophilic polymer that facilitates the subsequent reforming in the photocatalytic step. Therefore, high hydrogen production activity with a benchmark efficiency of >100 µmol g-1 h-1 was achieved. Moreover, the integrated process also demonstrates high versatility in upcycling different polyolefin plastics including polyethylene, polypropylene and polyvinyl chloride. The findings provide a new avenue for plastic upcycling in an efficient and sustainable way.

Fabrication of a ternary NiS/ZnIn2S4/g-C3N4 photocatalyst with dual charge transfer channels towards efficient H2 evolution.

As a renewable green energy, hydrogen has received widespread attention due to its huge potential in solving energy shortages and environment pollution. In this paper, a one-step solvothermal method was applied to grow ultra-thin g-C3N4 (UCN) nanosheets and NiS nanoparticles on the surface of ZnIn2S4 (ZIS). A ternary NiS/ZnIn2S4/ultra-thin-g-C3N4 composite material with dual high-speed charge transfer channels was constructed for the advancement of the photocatalytic H2 generation. The optimal ternary catalyst 1.5wt.%NiS/ZnIn2S4/ultra-thin-g-C3N4 (NiS/ZIS/UCN) achieved a H2 evolution yield reached to 5.02 mmolg-1h-1, which was 5.23 times superior than that of pristine ZnIn2S4 (0.96 mmolg-1h-1) and even outperform than that of the best precious metal modified 3.0 wt%Pt/ZnIn2S4 (4.08 mmolg-1h-1). The AQY at 420 nm could be achieved as high as 30.5%. The increased photocatalytic performance of NiS/ZIS/UCN could be ascribed to the type-I heterojunctions between intimated ZIS and UCN. In addition, NiS co-catalyst with large quantity of H2 evolution sites, could result in efficient photo-induced charges separation and migration. Furthermore, the NiS/ZIS/UCN composite exhibited excellent H2 evolution stability and recyclability. This work would also offer a reference for the design and synthesis of ternary co-catalyst with heterojunction composite for green energy conversion.

Fabrication of a dual S-scheme Bi7O9I3/g-C3N4/Bi3O4Cl heterojunction with enhanced visible-light-driven performance for phenol degradation.

S-scheme heterostructure can facilitate the separation of carriers while maintain outstanding redox capacity. A series of ternary Bi7O9I3/g-C3N4/Bi3O4Cl photocatalytic system was triumphantly synthesized via oil bath method in this work and used in photocatalytic degradation of phenol. The optimal TOC removal rate reached up to 93.57% under illumination for 160 min, which was slightly lower than phenol photodegradation (about 100%, 100 min). Correspondingly, the apparent rate constants for the decay of phenol are determined to be 0.0211 min-1. The experiment of free radical capture indicated that ·OH and ·O2- were the major oxidizing substances to degrade phenol. The products of phenol photodegradation were identified by high performance liquid chromatography (HPLC) and a possible degradation pathway was proposed. The characterization analysis and density functional theory (DFT) calculations demonstrated that dual S-scheme charge migration was generated at the interface of Bi7O9I3, g-C3N4 and Bi3O4Cl, contributing to an efficient separation of light-excited carriers. In the field of environmental remediation, the discovery of this work could open up promising vistas for designing bismuth-based ternary heterostructures with application potentiality.

A NiS co-catalyst decorated Zn3In2S6/g-C3N4 type-II ball-flower-like nanosphere heterojunction for efficient photocatalytic hydrogen production.

Promoting the separation of photogenerated electron-hole pairs and enhancing the charge carrier transfer are critical in photocatalysis. In our work, a ball-flower-like NiS/Zn3In2S6/g-C3N4 photocatalyst fabricated by a hydrothermal method exhibited superior performance for photocatalytic water splitting. The optimized 2.0% NiS/Zn3In2S6/g-C3N4 rivaled noble metal based Pt/g-C3N4 and showed an apparent quantum efficiency (AQE) of 24.3% at 420 nm, with a H2 yield of 4.135 mmol g-1 h-1, which was 30.4 and 9.51 times that of pure g-C3N4 and binary Zn3In2S6/g-C3N4 composites, respectively. The experimental and characterization results suggested that the heterojunction formed between Zn3In2S6/g-C3N4 and the decorating NiS co-catalyst cooperatively suppressed the electron-hole recombination and facilitated the charge carrier transfer, thus resulting in significant improvement of the H2 evolution performance. Moreover, the increased specific surface area and the enhanced visible-light absorption also contributed to superior water splitting performance. The prepared ternary catalytic system with the heterojunction and non-noble metal co-catalyst has great potential as an alternative to noble metals for achieving cost-efficient water splitting systems.

Recent Progress of Transition Metal Phosphides for Photocatalytic Hydrogen Evolution.

Photocatalytic hydrogen evolution can effectively alleviate the troublesome global energy crisis by converting solar energy into the chemical energy of hydrogen. In order to realize efficient hydrogen generation, a variety of semiconductor materials have been extensively investigated, including TiO2 , CdS, g-C3 N4 , metal-organic frameworks (MOFs), and others. In recent years, to achieve higher photocatalytic performance and reach the level of large-scale industrial applications, photocatalysts decorated with transition metal phosphides (TMPs) have shone brightly because of their low cost, stable physical and chemical properties, and substitution for precious metals of TMPs. This Review highlights the preparation methods and properties associated with photocatalysis of TMPs. Moreover, the H2 generation efficiency of photocatalysts loaded with TMPs and the roles of TMPs in catalytic systems are also studied systematically. Apart from being co-catalysts, several TMPs can also serve as host catalysts to boost the activity of photocatalytic composites. Finally, the development prospects and challenges of TMPs are put forward, which is valuable for future researchers to expand the application of TMPs in photocatalytic directions and to develop more active photocatalytic systems.