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Semiconducting metal oxide nanostructures for water splitting and photovoltaics
Luleå University of Technology, Department of Engineering Sciences and Mathematics, Material Science.ORCID iD: 0000-0003-1785-7177
Luleå University of Technology, Department of Engineering Sciences and Mathematics, Material Science. Dr. M. A. Kazi Institute of Chemistry University of Sindh Jamshoro, Sindh, Pakistan.ORCID iD: 0000-0002-6756-9862
Luleå University of Technology, Department of Engineering Sciences and Mathematics, Material Science.ORCID iD: 0000-0003-2935-1165
2017 (English)In: Advanced Energy Materials, ISSN 1614-6832, E-ISSN 1614-6840, Vol. 7, no 23Article in journal (Refereed) Published
Abstract [en]

Metal oxide (MOx) semiconducting nanostructures hold the potential for playing a critical role in the development of a new platform for renewable energies, including energy conversion and storage through photovoltaic effect, solar fuels, and water splitting. Earth-abundant MOx nanostructures can be prepared through simple and scalable routes and integrated in operating devices, which enable exploitation of their outstanding optical, electronic, and catalytic properties. In this review, the latest research results in this field are illustrated, highlighting the versatility of MOx nanostructures in meeting the stringent requirements to boost the efficiency of different systems. The functional properties inherently correlate to the morphology and the crystalline habit of MOx, which in most of the cases are organized in complex heterostructures. Tailoring the assembly of heterojunctions and their electronic band structure, the catalytic surface properties and the charge transport through complex networks represent the main challenge for the transition of MOx from the research to the real-life in the field of energy conversion and storage.

Place, publisher, year, edition, pages
John Wiley & Sons, 2017. Vol. 7, no 23
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Other Physics Topics
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Experimental Physics
Identifiers
URN: urn:nbn:se:ltu:diva-66889DOI: 10.1002/aenm.201700706ISI: 000423878500017Scopus ID: 2-s2.0-85041416503OAI: oai:DiVA.org:ltu-66889DiVA, id: diva2:1162278
Note

Validerad;2018;Nivå 2;2017-12-15 (andbra)

Available from: 2017-12-04 Created: 2017-12-04 Last updated: 2022-10-27Bibliographically approved

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