Recent Progress on Exploring Stable Metal–Organic Frameworks for Photocatalytic Solar Fuel Production
Solar energy, a clean and sustainable energy source, can be harvested and converted to solar fuel to meet the ever‐increasing energy demand. Integrating the photosensitizers and active catalytic sites into a single solid, metal–organic framework (MOF) with high void architectures and tunable chemica...
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Veröffentlicht in: | Solar RRL 2020-08, Vol.4 (8), p.n/a |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Solar energy, a clean and sustainable energy source, can be harvested and converted to solar fuel to meet the ever‐increasing energy demand. Integrating the photosensitizers and active catalytic sites into a single solid, metal–organic framework (MOF) with high void architectures and tunable chemical structures, is proposed as a promising platform for photocatalysis. However, compared with the traditional inorganic photocatalysts, the photocatalytic applications of MOFs are greatly hindered by its instability, especially the chemical instability. In this review, the background related to solar fuel production and MOFs are first discussed. Then, several strategies for designing stable MOFs are presented. Third, newly developed approaches for synthesizing highly efficient solar fuel production MOFs are summarized. Finally, the challenges and future perspectives using MOFs for solar fuel production are discussed. This review is expected to provide a deeper understanding of highly stable MOF design and new insights for the application of stable MOFs for solar fuel production.
Stable metal–organic frameworks (MOFs) are one of the best choices for a promising platform for photocatalytic solar fuel production due to its adjustable organic ligands and metal nodes, high void architectures, and tunable chemical structures. Possible strategies, such as organic linkers modulation, metal nodes modulation, and morphology and size modulation are summarized to design high‐efficiency and stable MOF photocatalysts. |
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ISSN: | 2367-198X 2367-198X |
DOI: | 10.1002/solr.201900547 |