Back to Search
Start Over
Hierarchical heterojunction comprising of in-situ derived TiO2 and salicylaldimine-supported Co catalysts in metal-organic frameworks for enhancing photocatalytic hydrogen generation.
- Source :
-
International Journal of Hydrogen Energy . Oct2024, Vol. 86, p236-244. 9p. - Publication Year :
- 2024
-
Abstract
- We present the design of a novel functional metal-organic framework here, denoted as Co-sal–NH 2 –MOF@TiO 2 , featuring the comprise of controllably in-situ grown TiO 2 sheets from NH 2 -MOF(Ti) and [Co] catalytic sites stabilized by salicylaldimine moiety via site isolation for visible-light-driven hydrogen evolution from water. The hierarchical organization of TiO 2 and Co catalyst within NH 2 -MOF (Ti) leads to outstanding photocatalytic performance, as evidenced by a H 2 yield of 15,584 μmolg−1h−1 and turnover numbers (TON) reaching 5844 over 24 h. This catalyst also signifies distinctly enhanced activities of approximately 105-fold, 354-fold, 15-fold, and 100-fold, compared to the pristine NH 2 -MOF(Ti), MOF-derived TiO 2 , NH 2 -MOF(Ti)@TiO 2 and the combination of [Co catalyst + NH 2 -MOF(Ti) + TiO 2 ], respectively. EXAFs and XPS etc. analyses revealed a stable coordination environment for salicylaldimine-supported Co(II) catalytic unit, which integrated with in-situ grown TiO 2 sheets can not only guarantee catalyst stability, but also generate much more densely packed light-harvesting heterojunction units and thus promote separation and transfer of photogenerated carriers between TiO 2 and Co catalyst in NH 2 -MOF(Ti) under light through optimized band gap structure. This work outlines the in-situ construction of organic and inorganic hybrid heterojunction for H 2 production from water. The novel organic and inorganic hybrid heterojunction that [Co] catalytic sites stabilized by salicylaldimine moiety with in-situ derived TiO 2 sheets from MOF(Ti) to realize further promoted visible light-driven H 2 formation. [Display omitted] • Salicylaldimine-supported Co and in-situ derived TiO 2 were integrated into NH 2 -MOF(Ti). • Co-sal–NH 2 –MOF@TiO 2 represented 105-fold enhanced H 2 evolution rate over pristine MOF. • EXAFs and XPS revealed stable coordination environment of Sal-Co and charge transfer pathway. • Synergistic effect between TiO 2 and Co in MOF endow high stability and mobility of charge carriers. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03603199
- Volume :
- 86
- Database :
- Academic Search Index
- Journal :
- International Journal of Hydrogen Energy
- Publication Type :
- Academic Journal
- Accession number :
- 179810282
- Full Text :
- https://doi.org/10.1016/j.ijhydene.2024.08.427