Ta3N5/CdS Core–Shell S-scheme Heterojunction Nanofibers for Efficient Photocatalytic Removal of Antibiotic Tetracycline and Cr(VI): Performance and Mechanism Insights

Artificial photosynthetic solar‐to‐chemical cycles enable an entire environment to operate in a more complex, yet effective, way to perform natural photosynthesis. However, such artificial systems suffer from a lack of well‐established photocatalysts with the ability to harvest the solar spectrum and rich catalytic active‐site density. Benefiting from extensive experimental and theoretical investigations, this bottleneck may be overcome by devising a photocatalytic platform based on metal sulfides with predominant electronic, physical, and chemical properties. These tunable properties can endow them with abundant active sites, favorable light utilization, and expedited charge transportation for solar‐to‐chemical conversion. Here, it is described how some vital lessons extracted from previous investigations are employed to promote the further development of metal sulfides for artificial photosynthesis, including water splitting, CO2 reduction, N2 reduction, and pollutant removal. Their functions, properties, synthetic strategies, emerging issues, design principles, and intrinsic functional mechanisms for photocatalytic redox reactions are discussed in detail. Finally, the associated challenges and prospects for the utilization of metal sulfides are highlighted and future development trends in photocatalysis are envisioned.

Recent Progress of Metal Sulfide Photocatalysts for Solar Energy Conversion

Designing oxygen vacancy mediated bismuth molybdate (Bi2MoO6)/N-rich carbon nitride (C3N5) S-scheme heterojunctions for boosted photocatalytic removal of tetracycline antibiotic and Cr(VI): Intermediate toxicity and mechanism insight.

A novel organic/inorganic S-scheme heterostructure of TCPP/Bi12O17Cl2 for boosting photodegradation of tetracycline hydrochloride: Kinetic, degradation mechanism, and toxic assessment

Simultaneous Dual-Functional Photocatalysis by g-C3N4-Based Nanostructures

Over the past few decades, graphitic carbon nitride (g-C3 N4 ) has arisen much attention as a promising candidate for photocatalytic hydrogen evolution reaction (HER) owing to its low cost and visible light response ability. However, the unsatisfied HER performance originated from the strong charge recombination of g-C3 N4 severely inhibits the further large-scale application of g-C3 N4 . In this case, the utilization of cocatalysts is a novel frontline in the g-C3 N4 -based photocatalytic systems due to the positive effects of cocatalysts on supressing charge carrier recombination, reducing the HER overpotential, and improving photocatalytic activity. This review summarizes some recent advances about the high-performance cocatalysts based on g-C3 N4 toward HER. Specifically, the functions, design principle, classification, modification strategies of cocatalysts, as well as their intrinsic mechanism for the enhanced photocatalytic HER activity are discussed here. Finally, the pivotal challenges and future developments of cocatalysts in the field of HER are further proposed.

Emerging Cocatalysts on g-C3N4 for Photocatalytic Hydrogen Evolution

One-pot in-situ hydrothermal synthesis of ternary In2S3/Nb2O5/Nb2C Schottky/S-scheme integrated heterojunction for efficient photocatalytic hydrogen production.

A new breakthrough in photocatalytic hydrogen evolution by amorphous and chalcogenide enriched cocatalysts

Incorporation of plasmonic metal nanomaterials can significantly enhance the visible light response of semiconductor photocatalysts via localized surface plasmon resonance (LSPR) mechanisms. However, the surfaces of plasmonic metal nanomaterials are often covered with surfactant molecules, which is undesired when the nanomaterials are used for photocatalytic hydrogen evolution, since surfactant molecules could significantly compromise the nanomaterials' cocatalyst functionalities by blocking the active sites and/or by inhibiting the surface charge transfer process. Herein, we demonstrate a method that assembles Au nanoparticles (NPs) into Au colloidosomes (AuCSs) without modifying their surfaces with surfactants. The resulting AuCSs were then coupled with CdS for the formation of Au-CdS composite photocatalysts through an in situ deposition method. The assembly of Au NPs induced a broader and stronger LSPR response for AuCSs, while the absence of surfactants allowed them to act efficiently as cocatalysts. This essentially enhanced the electron-hole pair generation rate and further their utilization efficiency, leading to an extremely high hydrogen evolution rate of 235.8 mmol·g-1·h-1 under simulated sunlight excitation.

Rational Synthesis of Au-CdS Composite Photocatalysts for Broad-Spectrum Photocatalytic Hydrogen Evolution.

As one of the most promising photocatalysts for H2 evolution, graphitic carbon nitride (CN) has many appealing attributes including tunable electronic structure, excellent physicochemical stability, and low synthetic cost. However, the activity of pristine CN remains unsatisfactory due to severe charge carrier recombination and lack of active sites. In this study, we report a two-step approach for synthesis of CN nanotubes (TCN) loaded with NiS nanoparticles. The resulting composite photocatalysts gave a H2 evolution rate of 752.9 μmol g−1 h−1, which is 42.3 times higher compared to the pristine CN photocatalyst. Experimental and simulation results showed that the Schottky junction which was formed between TCN and NiS was key to achieving high activity. This is because the formation of Schottky junction prevented the backflow of electrons from NiS to TCN, which improved charge separation efficiency. More importantly, it also led to the accumulation of electrons on NiS, which significantly weakens the SH bond, such that the intermediate hydrogen species can more easily desorbed from NiS surface to promote H2 evolution activity. 

Schottky junction enhanced H2 evolution for graphitic carbon nitride-NiS composite photocatalysts

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