The global shortage of freshwater resources and the energy crisis have propelled solar-driven interfacial evaporation (SDIE) coupled with photocatalytic technology to become a research focus in efficient and low-carbon water treatment. Graphene-based materials demonstrate unique advantages in SDIE–photocatalysis integrated systems, owing to their broadband light absorption, ultrafast thermal carrier dynamics, tunable electronic structure, and low evaporation enthalpy characteristics. This review systematically investigates the enhancement mechanisms of graphene photothermal conversion on photocatalytic processes, including (1) improving light absorption through surface morphology modulation, defect engineering, and plasmonic material compositing; (2) reducing water evaporation enthalpy via hydrophilic functional group modification and porous structure design; (3) suppressing heat loss through thermal insulation layers and 3D structural optimization; and (4) enhancing water transport efficiency via fluid channel engineering and wettability control. Furthermore, salt resistance strategies and structural optimization significantly improve system practicality and stability. In water treatment applications, graphene-based SDIE systems achieve synergistic “adsorption–catalysis–evaporation” effects, enabling efficient the degradation of organic pollutants, reduction in/fixation of heavy metal ions, and microbial inactivation. However, practical implementation still faces challenges including low steam condensation efficiency, insufficient long-term material durability, and high scaling-up costs. Future research should prioritize enhancing heat and mass transfer in condensation systems, optimizing material environmental adaptability, and developing low-cost manufacturing processes to promote widespread application of graphene-based SDIE–photocatalysis integrated systems.

Against the backdrop of increasing global warming, exploring sustainable pathways to mitigate the greenhouse effect has become a central issue for the ecological and energy future. Photocatalytic reduction of CO₂ technology shows a broad application prospect due to its ability to directly convert CO₂ into high-value-added hydrocarbon fuels and to use solar energy, a clean energy source, to drive the reaction. However, traditional semiconductor catalysts generally suffer from insufficient activity and poor product selectivity in the actual reaction, which cannot meet the requirements of practical applications. In recent years, sulfur vacancy, as an effective material modulation strategy, has demonstrated a remarkable role in enhancing photocatalytic performance. This paper reviews a series of research reports on sulfur vacancies in recent years, introduces the methods of preparing sulfur vacancies, and summarizes the commonly used characterization methods of sulfur vacancies. Finally, the mechanism of introducing sulfur vacancies to promote CO₂ reduction is discussed, which improves the photocatalytic activity and selectivity by enhancing light absorption, facilitating carrier separation, improving CO₂ adsorption and activation, and promoting the stability of reaction intermediates. This review aims to provide theoretical support for an in-depth understanding of the role of sulfur vacancies in photocatalytic systems and to provide a view on the future direction and potential challenges of sulfur vacancies.

This study provides valuable insights into the oxidative vs. basic asynchronous CPET mechanisms of HAT reactions to exhibit reversed electronic substitution effects on HAT reactions of Mn(iii)-hydroxo and Mn(iii)-aqua complexes.

Converting carbon dioxide (CO₂) into high-value fuels through the photothermal effect offers an effective approach to enhancing the carbon cycle and reducing the greenhouse effect. In this study, we developed Ag/C-TCN-x, a carbon nitride-based photocatalyst that integrates both photothermal and localized surface plasmon resonance (LSPR) effects. This material was synthesized through a three-step process involving hydrothermal treatment, calcination, and photo-deposition. Real-time infrared thermography monitoring revealed that Ag/C-TCN-2 reached a surface stabilization temperature of approximately 176 °C, which was 1.5 times higher than C-TCN and 2.2 times higher than g-C₃N₄. Under the same experimental conditions, Ag/C-TCN demonstrated a carbon monoxide (CO) release rate 3.3 times greater than that of pure g-C₃N₄. The composite sample Ag/C-TCN-2 maintained good photocatalytic activity in five cycling tests. The structural stability of the sample after the cycling tests was confirmed by X-ray diffraction (XRD) test. The unique tubular structure of Ag/C-TCN increased its specific surface area, facilitating enhanced CO₂ adsorption. Carbon doping not only triggered the photothermal effect but also accelerated the conversion of carriers. Additionally, the LSPR effect of Ag nanoparticles, combined with carbon doping, optimized charge carrier dynamics and promoted efficient CO₂ photoreduction. The CO₂ reduction mechanism over Ag/C-TCN was further examined using in situ Fourier Transform Infrared (FT-IR) spectroscopy. This research offers valuable insights into how photothermal and LSPR effects can be harnessed to enhance the efficiency of CO₂ photoreduction.