光催化
纳米复合材料
钴
氮化碳
材料科学
酞菁
碳纤维
氮化物
氢
化学工程
制氢
纳米技术
化学
冶金
复合材料
复合数
催化作用
有机化学
工程类
图层(电子)
作者
Lakshman Sundar Arumugam,Javier E. Durantini,Jorge Follana‐Berná,Frederik Schiller,Ane Etxebarria,Lorenzo Forzanini,Sara Barja,Ángela Sastre‐Santos,Sixto Giménez
标识
DOI:10.1021/acsaem.4c03257
摘要
The photocatalytic production of hydrogen stands out as a promising strategy to convert and store solar energy as chemical energy in the form of a sustainable energy carrier. In the present study, a hybrid photocatalyst based on cobalt phthalocyanine (CoPc) coupled with polymeric carbon nitride (CN) is synthesized using a simple, cost-effective, and upscalable method. Both components are held together in the hybrid nanocomposite via π–π interactions, as shown by detailed structural and optical characterization. The synergistic interaction between both components, CN, a metal-free semiconductor, valued for its stability and tunable electronic properties, and CoPc, known for its excellent light absorption and electronic properties, is evidenced in a proof-of-concept photocatalytic reaction: the photo-oxidation of benzyl alcohol (BzOH) to benzaldehyde (BzO). Chemical trapping reagents were employed to elucidate the reaction mechanism, showing favorable recombination dynamics of the hybrid photocatalyst (CoPc/CN) compared to the individual components. Furthermore, photocatalytic hydrogen production was conducted in an aqueous solution using triethanolamine (TEOA) as an electron donor, with the optimized CoPc/CN nanocomposite producing 1136.5 μmol h–1 gcat–1 of H2, achieving a 50% higher hydrogen yield compared to pristine CN. These results contribute to the design of high-performance photocatalytic materials for promising solar-to-X transformations.
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