Cargando…

Confining charge-transfer complex in a metal-organic framework for photocatalytic CO(2) reduction in water

In the quest for renewable fuel production, the selective conversion of CO(2) to CH(4) under visible light in water is a leading-edge challenge considering the involvement of kinetically sluggish multiple elementary steps. Herein, 1-pyrenebutyric acid is post-synthetically grafted in a defect-engine...

Descripción completa

Detalles Bibliográficos
Autores principales: Karmakar, Sanchita, Barman, Soumitra, Rahimi, Faruk Ahamed, Rambabu, Darsi, Nath, Sukhendu, Maji, Tapas Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371996/
https://www.ncbi.nlm.nih.gov/pubmed/37495574
http://dx.doi.org/10.1038/s41467-023-40117-z
Descripción
Sumario:In the quest for renewable fuel production, the selective conversion of CO(2) to CH(4) under visible light in water is a leading-edge challenge considering the involvement of kinetically sluggish multiple elementary steps. Herein, 1-pyrenebutyric acid is post-synthetically grafted in a defect-engineered Zr-based metal organic framework by replacing exchangeable formate. Then, methyl viologen is incorporated in the confined space of post-modified MOF to achieve donor-acceptor complex, which acts as an antenna to harvest visible light, and regulates electron transfer to the catalytic center (Zr-oxo cluster) to enable visible-light-driven CO(2) reduction reaction. The proximal presence of the charge transfer complex enhances charge transfer kinetics as realized from transient absorption spectroscopy, and the facile electron transfer helps to produce CH(4) from CO(2). The reported material produces 7.3 mmol g(−1) of CH(4) under light irradiation in aqueous medium using sacrificial agents. Mechanistic information gleans from electron paramagnetic resonance, in situ diffuse reflectance FT-IR and density functional theory calculation.