ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 10480 - 10520
Published: June 5, 2025
Language: Английский
ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 10480 - 10520
Published: June 5, 2025
Language: Английский
Applied Catalysis B Environment and Energy, Journal Year: 2025, Volume and Issue: unknown, P. 125289 - 125289
Published: March 1, 2025
Language: Английский
Citations
2Small, Journal Year: 2025, Volume and Issue: unknown
Published: March 4, 2025
Abstract Photocatalytic reduction of CO 2 to high‐value‐added chemicals represents a promising strategy for effective utilization, and rationally regulating the electronic structure catalyst is key enhancing photocatalytic performance. Herein, it demonstrated that in situ doping atomic indium into lattice Cu MoS 4 results remarkable enhancements A record gas product yield 104.1 µmol·g −1 ·h achieved under visible light irradiation (>420 nm), accompanied by generation rate 35.3 ethylene. Detailed experimental analyses density functional theory (DFT) calculations reveal low electronegativity atoms induces asymmetric charge redistribution near sites. This effect facilitates adsorption dissociation molecules at charge‐enriched Mo sites, as well subsequent intermediates ( * COCOH) toward ethylene formation. work advances understanding potential mechanism between active site performance, providing valuable insights fabricating advanced materials conversion solar fuels.
Language: Английский
Citations
0Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown
Published: March 7, 2025
Abstract The “Solar Sabatier” reaction has emerged as a promising sustainable method for the CO 2 hydrogenation. development of advanced metal‐support catalysts based on Strong Metal‐Support Interaction (SMSI) offers significant advantages in activation and regulation selectivity. Herein, novel composite Ni/CaTiO 3 catalyst consisting Ni Ni‐doped CaTiO is synthesized utilized methanation. A noteworthy finding that incorporation into matrix instrumental formation oxygen vacancies establishment SMSI between . enhanced resulting from surface‐doped atoms not only facilitated effective interface contact metallic surface but also significantly improved migration efficiency hydrogen reduced barrier methanation optimized rate‐limiting step, all which are advantageous Consequently, exhibited extraordinary performance, achieving conversion rate 87.77%, CH 4 generation 3.12 mol g −1 h , ≈100% selectivity under ambient pressure conditions. This investigation lays groundwork design highly active understanding mechanisms underlying SMSI.
Language: Английский
Citations
0Inorganic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: April 20, 2025
Photocatalytic conversion of CO2 into chemical fuels has emerged as a research hotspot, aiming to mitigate the rapid depletion fossil and alleviate global warming. However, inherent low carrier separation efficiency limited solar light utilization photocatalysts lead unsatisfactory efficiency. In this study, an appealing CuCo2S4/g-C3N4-x S-scheme heterostructure is successfully fabricated by simple polyol reflux method. Notably, nitrogen vacancies enhance Fermi level difference between CuCo2S4 g-C3N4-x, resulting in stronger interfacial built-in electric field. The full-spectrum strong optical absorption capability endows synthesized catalysts with superior light-harvesting property. photothermal effect-induced temperature increase accelerates cyclic process adsorption CO desorption on catalyst surface. Most importantly, charge transfer pathway ensures efficient photogenerated carriers. Thanks these synergistic benefits, exhibits exceptional photothermal-assisted photocatalytic reduction performance. Under simulated sunlight, average production rate reaches 24.64 μmol g-1 h-1, which 12.1 27.1 times higher than that g-C3N4 CuCo2S4, respectively. This study offers novel strategy for designing outstanding
Language: Английский
Citations
0Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown
Published: May 5, 2025
Abstract Covalent–organic frameworks (COFs) based heterojunctions photocatalytic have showed great potential for CO 2 upcycling. Currently, significant progress has been made in developing such photocatalysts, yet a comprehensive understanding of this field remains lacking. This review systematically explores the inherent relationship between COF‐based heterojunction innovations and CO₂ reduction, aiming to establish structure–performance–mechanism correlation that guides design high‐efficiency catalysts. First, fundamentals, mechanisms, related principles conversion, as well advantages COFs application, are thoroughly introduced. Then, state‐of‐the‐art applied reduction discussed from following critical aspects: interfacial engineering, spatial charge transfer regulation, active component hybridization, half‐reaction kinetic optimization, sites engineering. Subsequently, systematic overview characterization techniques research methodologies probing catalyst structures in‐depth reaction mechanisms is outlined. Finally, challenges further development direction proposed. It expected can provide powerful guidance reference toward exploiting high‐performance photocatalysts conversion.
Language: Английский
Citations
0Catalysts, Journal Year: 2025, Volume and Issue: 15(6), P. 562 - 562
Published: June 5, 2025
Covalent triazine frameworks (CTFs) are a class of porous organic semiconductors containing large number units, which gives them many properties suitable for photocatalysis, such as high porosity, good tunability, and excellent chemical stability. However, it is difficult to achieve activity, stability, selectivity at the same time using single CTF in specific catalytic reaction. Therefore, necessary find ways combine CTFs with other materials improve their photocatalysis activity. From this perspective, some construction methods latest progress CTF-based composites presented, applications field introduced. Finally, future proposed, provides insights into research exploration composites.
Language: Английский
Citations
0ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 10480 - 10520
Published: June 5, 2025
Language: Английский
Citations
0