Please use this identifier to cite or link to this item: https://doi.org/10.1039/c9na00540d
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dc.titleBa-addition induced enhanced surface reducibility of SrTiO3: implications on catalytic aspects
dc.contributor.authorJain, N.
dc.contributor.authorRoy, A.
dc.contributor.authorDe, A.
dc.date.accessioned2021-12-16T07:52:08Z
dc.date.available2021-12-16T07:52:08Z
dc.date.issued2019
dc.identifier.citationJain, N., Roy, A., De, A. (2019). Ba-addition induced enhanced surface reducibility of SrTiO3: implications on catalytic aspects. Nanoscale Advances 1 (12) : 4938-4946. ScholarBank@NUS Repository. https://doi.org/10.1039/c9na00540d
dc.identifier.issn25160230
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/210819
dc.description.abstractSurface reducibility engineering is one of the vital tools to enhance the catalytic activity of materials. A heavy redox treatment can be utilized to affect the structure and surface of catalytic materials. Here, we choose SrTiO3 (STO) with a cubic perovskite structure as a system to induce oxygen vacancies by using nascent hydrogen from NaBH4 leading to a heavily reduced version of SrTiO3 (RSTO). To further understand the surface reduction and its dependence on foreign-ion (Ba) incorporation into SrTiO3, Sr0.5Ba0.5TiO3 (SBTO) and BaTiO3 (BTO) are synthesized using a facile hydrothermal method. The reduced version of the pristine and mixed oxide shows distinct optical absorptions, indicating oxygen vacancy-mediated reducibility engineering. Detailed CO oxidation experiments suggest the order of activity over the as-prepared and reduced supports as STO > SBTO > BTO and RSBTO > RSTO > RBTO, respectively. The interesting observation of reversal of CO oxidation activity over STO and SBTO after reduction negates the assumption of a similar intensity of reduction on the surfaces of these oxide supports. The fundamental aspect of surface reducibility is addressed using temperature programmed reduction/oxidation (TPR/TPO) and XPS. © 2019 The Royal Society of Chemistry.
dc.publisherRoyal Society of Chemistry
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScopus OA2019
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1039/c9na00540d
dc.description.sourcetitleNanoscale Advances
dc.description.volume1
dc.description.issue12
dc.description.page4938-4946
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