The persistent issue of CO emissions and their subsequent impact on the Earth's atmosphere can be effectively addressed through the utilization of efficient photocatalysts. Employing a sustainable carbon cycle via photocatalysis presents a promising technology for simultaneously managing the greenhouse effect and the energy dilemma. However, the efficiency of energy conversion encounters limitations due to inadequate carrier utilization and a deficiency of reactive sites. Single-atom catalysts (SACs) have demonstrated exceptional performance in efficiently addressing the aforementioned challenges. This review article commences with an overview of SAC types, structures, fundamentals, synthesis strategies, and characterizations, providing a logical foundation for the design and properties of SACs based on the correlation between their structure and efficiency. Additionally, we delve into the general mechanism and the role of SACs in photocatalytic CO reduction. Furthermore, we furnish a comprehensive survey of the latest advancements in SACs concerning their capacity to enhance efficiency, long-term stability, and selectivity in CO reduction. Carbon-structured support materials such as covalent organic frameworks (COFs), graphitic carbon nitride (g-CN), metal-organic frameworks (MOFs), covalent triazine frameworks (CTFs), and graphene-based photocatalysts have garnered significant attention due to their substantial surface area, superior conductivity, and chemical stability. These carbon-based materials are frequently chosen as support matrices for anchoring single metal atoms, thereby enhancing catalytic activity and selectivity. The motivation behind this review article lies in evaluating recent developments in photocatalytic CO reduction employing SACs supported on carbon substrates. In conclusion, we highlight critical issues associated with SACs, potential prospects in photocatalytic CO reduction, and existing challenges. This review article is dedicated to providing a comprehensive and organized compilation of recent research findings on carbon support materials for SACs in photocatalytic CO reduction, with a specific focus on materials that are environmentally friendly, readily accessible, cost-effective, and exceptionally efficient. This work offers a critical assessment and serves as a systematic reference for the development of SACs supported on MOFs, COFs, g-CN, graphene, and CTFs support materials to enhance photocatalytic CO conversion.
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http://dx.doi.org/10.1016/j.cis.2023.103068 | DOI Listing |
Dalton Trans
January 2025
National Forestry and Grassland Administration Key Laboratory of Plant Fiber Functional Materials, College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
The unique benefits of nickel-aluminium layered double hydroxide (Ni-Al LDH)-based heterojunctions, including large surface area, tunable bandgap and morphology, abundant reaction sites, and high activity, selectivity, and photostability, make them extremely promising for photocatalytic applications. Given the importance and benefits of Ni-Al LDH-based heterojunctions in photocatalysis, it is necessary to provide a summary of Ni-Al LDH-based heterojunctions for photocatalytic applications. Hence, in this review, we thoroughly described the material design for Ni-Al LDH-based heterojunctions, along with their recent developments in various photocatalytic applications, , H evolution, CO reduction, and pollutant removal.
View Article and Find Full Text PDFDalton Trans
January 2025
College of Life Sciences, School of Chemical Engineering, Key Laboratory of Green Catalysis of Jiangxi Education Institutes, Jiangxi Normal University, Nanchang 330022, China.
The photocatalytic conversion of CO and HO into useful chemicals or fuels over semiconductor photocatalysts is regarded as a promising technology to address the problems of global warming and energy exhaustion. However, inefficient photo-absorption and slow charge dynamics limit the CO photoreduction efficiency. Here, a ternary heterojunction photocatalyst, CuCl(OH)/In/InO (Cu H IO), with an intimate interface is obtained a hydrogen chemical reduction approach followed by hydrolysis reaction, where In species can be produced on the surface of InO from the hydrogen chemical reaction with a calcining temperature of over 500 °C.
View Article and Find Full Text PDFSci Rep
January 2025
School of Metallurgy and Materials Engineering, Iran University of Science and Technology, Narmak, Tehran, Iran.
In this study, in situ-synthesized ZnO/g-CN based composites were used as photocatalysts for organic pollution removal. These nanocomposites were prepared through simple calcination of a mixture of melamine and ZnO nanoparticles and underwent comprehensive evaluation of their structural, morphological, optical, and photocatalytic properties, using various analytical techniques. As the g-CN content increased, the band gap decreased from 3.
View Article and Find Full Text PDFNat Commun
January 2025
Key Laboratory of Photochemistry, Institute of Chemistry Chinese Academy of Sciences, Beijing National Laboratory for Molecular Sciences, Beijing, PR China.
To enable open environment application of artificial photosynthesis, the direct utilization of environmental CO via an oxygen-tolerant reductive procedure is necessary. Herein, we introduce an in situ growth strategy for fabricating two-dimensional heterojunctions between indium porphyrin metal-organic framework (In-MOF) and single-layer graphene oxide (GO). Upon illumination, the In-MOF/GO heterostructure facilitates a tandem CO capture and photocatalytic reduction on its hydroxylated In-node, prioritizing the reduction of dilute CO even in the presence of air-level O.
View Article and Find Full Text PDFLangmuir
January 2025
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Oxygen and water generating hydrogen peroxide (HO) by optical drive is an extremely promising pathway, and the large amount of oxygen in air and natural sunlight illumination are excellent catalytic conditions. However, the separation efficiency of photogenerated electron-hole pairs greatly limits the photocatalytic efficiency, especially in the absence of sacrificial agents. Here, we report an InS nanosheet with an S vacancy (S-InS).
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