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Co-MOF as a sacrificial template: manifesting a new Co 3 O 4 /TiO 2 system with a p–n heterojunction for photocatalytic hydrogen evolution

The present work reports a novel method for preparing an elusive Co 3 O 4 /TiO 2 p–n heterojunction using Co-based metal organic frameworks (Co-MOFs) as a TiO 2 -absorbent cum sacrificial template for nanocomposite formation. Four new Co-MOFs based on a bispyrazole ligand and different carboxylic ac...

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Bibliographic Details
Published in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2015, Vol.3 (40), p.20288-20296
Main Authors: Bala, Sukhen, Mondal, Indranil, Goswami, Arijit, Pal, Ujjwal, Mondal, Raju
Format: Article
Language:English
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Summary:The present work reports a novel method for preparing an elusive Co 3 O 4 /TiO 2 p–n heterojunction using Co-based metal organic frameworks (Co-MOFs) as a TiO 2 -absorbent cum sacrificial template for nanocomposite formation. Four new Co-MOFs based on a bispyrazole ligand and different carboxylic acids, with a wide variety of dimensionality, porosity and surface characteristics, were exploited for this purpose. We detail here the synthesis of cobalt MOFs using the hydro(solvo)thermal method and structural characterization by single crystal X-ray diffraction (XRD). We have also successfully demonstrated our strategy of using MOFs for fabricating superior p–n diode-type Co 3 O 4 /TiO 2 hetero-nanocomposites for photocatalytic hydrogen production. The characterization results suggested that the nanocomposites consisted of highly crystalline desired anatase TiO 2 nanoparticles and spinel Co 3 O 4 -like species. The nanocomposite with 2 wt% Co loading exhibited the maximum photoactivity with a hydrogen evolution rate of ∼7 mmol g −1 h −1 under UV-vis light irradiation. The above results indicate that the present preparative strategy is an amenable route for the synthesis of desirable synergistic photocatalysts combining a remarkable reactivity relevant to solar energy conversion.
ISSN:2050-7488
2050-7496
DOI:10.1039/C5TA05210F