4.6 Article

Exfoliation and thermal transformations of Nb-substituted layered titanates

期刊

JOURNAL OF SOLID STATE CHEMISTRY
卷 184, 期 12, 页码 3135-3143

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jssc.2011.08.039

关键词

Nb-substitution; Nanosheets; Exfoliation; Restacking; Ultrasonication

资金

  1. Research Council of Norway (NANOMAT) [163565 431]

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Single-layer Nb-substituted titanate nanosheets of ca. 1 nm thickness were obtained by exfoliating tetrabutylammonium (TBA)-intercalated Nb-substituted titanates in water. AFM images and turbidity measurements reveal that the exfoliated nanosheets crack and corrugate when sonicated. Upon heating, the thermal transformation into anatase and further to rutile is retarded. This suppression of the phase transition upon higher valent substitution may promote technological applications of anatase thin films, hereunder development of films with TCO properties. Depending on the oxygen partial pressure during the transformation, the Nb-substitution into TiO2 provokes different defect situations and also electronic properties. At reducing conditions, Nb is incorporated as Nb-V and an equivalent amount of Ti-IV is transformed to Ti-III as evidenced by XPS. Magnetic susceptibility data show accordingly paramagnetic behavior. For samples heated in air Ti-IV and Nb-V cations prevail, the latter is compensated by cation vacancies. Nb-93 MAS NMR data prove that Nb is finely dispersed into the transformed (Ti,Nb)O-2 oxide matrices without sign of Nb2O5 (nano)precipitates. The Nb-O-Ti bonds and defects at cation sites are considered key factors for increasing the transformation temperatures for conversion of the nanosheets to anatase and finally into rutile. It is further tempting to link the delay in crystallization to morphology limitations originating from the nanosheets. The present work shows that layered Nb-titanates are appropriate precursors for formation of highly oriented Nb-substituted anatase thin films via delamination, reconstruction and subsequent heat treatment. (C) 2011 Elsevier Inc. All rights reserved.

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