Please use this identifier to cite or link to this item: https://doi.org/10.1063/5.0005648
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dc.titleStrain-tunable III-nitride/ZnO heterostructures for photocatalytic water-splitting: A hybrid functional calculation
dc.contributor.authorZhang, Z.
dc.contributor.authorHuang, B.
dc.contributor.authorQian, Q.
dc.contributor.authorGao, Z.
dc.contributor.authorTang, X.
dc.contributor.authorLi, B.
dc.date.accessioned2021-08-19T04:35:46Z
dc.date.available2021-08-19T04:35:46Z
dc.date.issued2020
dc.identifier.citationZhang, Z., Huang, B., Qian, Q., Gao, Z., Tang, X., Li, B. (2020). Strain-tunable III-nitride/ZnO heterostructures for photocatalytic water-splitting: A hybrid functional calculation. APL Materials 8 (4) : 41114. ScholarBank@NUS Repository. https://doi.org/10.1063/5.0005648
dc.identifier.issn2166-532X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/198096
dc.description.abstractSolar to fuel energy conversion is one of the momentous topics nowadays considering the urgent demand for clean energy supplies. In this work, the tunable electronic and optical properties of III-nitride/ZnO 2D/2D heterostructures (including GaN/ZnO, AlN/ZnO, and GaN/AlN) by strain engineering were investigated by first-principles calculations. The studied heterostructures feature a small interlayer distance, with the cation of one layer directly above the anion of the other layer, and vice versa. This leads to a strong binding energy and interlayer coupling across the heterostructure. The built-in field induced by the charge redistribution facilitates the photoexcited carrier migration, which is beneficial to the photocatalytic water splitting application. The stable III-nitride/ZnO heterostructures exhibit decent band edge positions with biaxial strain engineering and feature an enhancement of optical absorption under tensile strain. Our results indicate that the III-nitride/ZnO 2D/2D heterostructures are promising photocatalysts for solar to hydrogen generation by water splitting. © 2020 Author(s).
dc.publisherAmerican Institute of Physics Inc.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2020
dc.typeArticle
dc.contributor.departmentDEPT OF PHYSICS
dc.description.doi10.1063/5.0005648
dc.description.sourcetitleAPL Materials
dc.description.volume8
dc.description.issue4
dc.description.page41114
dc.published.statePublished
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