Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9423
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dc.contributor.authorPathak, Biswarupen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:58Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:58Z-
dc.date.issued2013-
dc.identifier.citationLiu, P., Nisar, J., Sa, B., Pathak, B., & Ahuja, R. (2013). Anion-anion mediated coupling in layered perovskite La2Ti 2O7 for visible light photocatalysis. Journal of Physical Chemistry C, 117(27), 13845-13852. doi:10.1021/jp402971ben_US
dc.identifier.issn1932-7447-
dc.identifier.otherEID(2-s2.0-84880178847)-
dc.identifier.urihttps://doi.org/10.1021/jp402971b-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9423-
dc.description.abstractAnionic-anionic (N-N, P-P, N-P, and C-S) mediated coupling can be introduced in the layered perovskite La2Ti2O7 structure for visible light photocatalysis. The anionic-anionic codoped La 2Ti2O7 systems lower the band gap much more than their respective monodoping systems. Moreover, the electronic band positions of the doped systems with respect to the water oxidation/reduction potentials show that codoped (N-N, N-P, and C-S) systems are more promising candidates for visible-light photocatalysis. The calculated defect formation energy shows that the codoped systems are more stable than their respective monodoped systems. © 2013 American Chemical Society.en_US
dc.language.isoenen_US
dc.sourceJournal of Physical Chemistry Cen_US
dc.subjectCo-dopeden_US
dc.subjectDefect formation energiesen_US
dc.subjectDoped systemsen_US
dc.subjectElectronic banden_US
dc.subjectLayered perovskiteen_US
dc.subjectVisible-light photocatalysisen_US
dc.subjectWater oxidationen_US
dc.subjectPerovskiteen_US
dc.subjectPhotocatalysisen_US
dc.subjectDoping (additives)en_US
dc.titleAnion-anion mediated coupling in layered perovskite La2Ti 2O7 for visible light photocatalysisen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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