Engineering of Graphitic Carbon Nitride (g-C3N4) Based Photocatalysts for Atmospheric Protection: Modification Strategies, Recent Progress, and Application Challenges.

Graphitic carbon nitride (g-C3N4) is a prominent photocatalyst that has attracted substantial interest in the field of photocatalytic environmental remediation due to the low cost of fabrication, robust chemical structure, adaptable and tunable energy bandgaps, superior photoelectrochemical properties, cost-effective feedstocks, and distinctive framework. Nonetheless, the practical application of bulk g-C3N4 in the photocatalysis field is limited by the fast recombination of photogenerated e--h+ pairs, insufficient surface-active sites, and restricted redox capacity. Consequently, a great deal of research has been devoted to solving these scientific challenges for large-scale applications. This review concisely presents the latest advancements in g-C3N4-based photocatalyst modification strategies, and offers a comprehensive analysis of the benefits and preparation techniques for each strategy. It aims to articulate the complex relationship between theory, microstructure, and activities of g-C3N4-based photocatalysts for atmospheric protection. Finally, both the challenges and opportunities for the development of g-C3N4-based photocatalysts are highlighted. It is highly believed that this special review will provide new insight into the synthesis, modification, and broadening of g-C3N4-based photocatalysts for atmospheric protection.

Advancements in Electrocatalytic Nitrogen Reduction: A Comprehensive Review of Single-Atom Catalysts for Sustainable Ammonia Synthesis.

Electrocatalytic nitrogen reduction technology seamlessly aligns with the principles of environmentally friendly chemical production. In this paper, a comprehensive review of recent advancements in electrocatalytic NH3 synthesis utilizing single-atom catalysts (SACs) is offered. Into the research and applications of three categories of SACs: noble metals (Ru, Au, Rh, Ag), transition metals (Fe, Mo, Cr, Co, Sn, Y, Nb), and nonmetallic catalysts (B) in the context of electrocatalytic ammonia synthesis is delved. In-depth insights into the material preparation methods, single-atom coordination patterns, and the characteristics of the nitrogen reduction reaction (NRR) are provided. The systematic comparison of the nitrogen reduction capabilities of various SAC types offers a comprehensive research framework for their integration into electrocatalytic NRR. Additionally, the challenges, potential solutions, and future prospects of incorporating SACs into electrocatalytic nitrogen reduction endeavors are discussed.

Pulsed versus direct current electrochemical co-catalytic peroxymonosulfate-based system: Elevated degradation and energy efficiency with enhanced oxidation mechanisms.

In this work, the pulsed electrochemical (PE) system was investigated to activate peroxymonosulfate (PMS) with the addition of Fe(III) to achieve efficient degradation of sulfamethoxazole (SMX) with reduced energy consumption, in comparison with the direct current (DC) electrochemical system. The operational conditions of PE/PMS/Fe(III) system were optimized as 4 kHz pulse frequency, 50% duty cycle, and pH 3, at which 67.6% reduction of energy consumption and enhanced degradation performance were achieved compared to the DC/PMS/Fe(III) system. Results of electron paramagnetic resonance spectroscopy analysis and quenching and chemical probe experiment revealed the presence of •OH, SO4•-, and 1O2 in the system, with •OH being the dominant role. The concentrations of these active species were averagely 15 ± 1% higher in the PE/PMS/Fe(III) system than those of the DC/PMS/Fe(III) system. Identification of SMX byproducts was achieved based on high resolution mass spectrometry analysis to predict the degradation pathways. The SMX byproducts could eventually be eliminated by the PE/PMS/Fe(III) system with extended treatment time. Overall, the PE/PMS/Fe(III) system was demonstrated with high energy and degradation performance, and is appear to be an robust strategy for practical treatment of wastewater.

Identifying the evolution of primary oxidation mechanisms and pollutant degradation routes in the electro-cocatalytic Fenton-like systems.

Herein, electro-catalysis (EC) as the electron donor to accelerate the continuable Fe(III)/Fe(II) cycles in different inorganic peroxides (i.e., peroxymonosulfate (PMS), peroxydisulfate (PDS) and hydrogen peroxide (HP)) activation systems were established. These electro-cocatalytic Fenton-like systems exhibited an excellent degradation efficiency of sulfamethoxazole (SMX). A series of analytical and characterization methods including quenching experiments, probe experiments, and electron paramagnetic resonance spectrometry (EPR) were implemented to systematically sort out the source and yield of reactive oxygen species (ROS). A wide kind of ROS including hydroxyl radical (•OH), singlet oxygen (1O2), and sulfate radical (SO4•-), which contributed 38%, 37%, and 24% were produced in EC/Fe(III)/PMS system, respectively. •OH was the dominant ROS in both EC/Fe(III)/PDS and EC/Fe(III)/HP processes. According to the analysis of SMX degradation routes and biotoxicity, abundant degradation pathways were identified in EC/Fe(III)/PMS process and lower environmental impact was achieved in EC/Fe(III)/HP process. The diversiform ROS of EC/Fe(III)/PMS system makes it exhibit greater environmental adaptability in complex water matrixes and excellent low-energy consumption performance in many organic pollutants degradation. Continuous flow treatment experiments proved that the three systems have great sustainability and practical application prospect. This work provides a strong basis for constructing suitable systems to achieve different treatment requirements.