Experimental and simulation-based understanding of morphology controlled barium titanate nanoparticles under co-adsorption of surfactants. Issue 24 (2nd June 2017)

• Record Type: Journal Article
• Authors: Sun, Zhongyu; Zhang, Lei; Dang, Feng; Liu, Yao; Fei, Zhiying; Shao, Qian; Lin, Hong; Guo, Jiang; Xiang, Lichen; Yerra, Narendranath; Guo, Zhanhu
• Is Part Of: CrystEngComm. Volume 19:Issue 24(2017)
• Page Start: 3288
• Page End: 3298
• Publication Date: 2017-06-02
• Subjects: Crystals -- Periodicals; Crystal growth -- Periodicals; Crystallography -- Periodicals; Cristaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Cristallographie -- Périodiques; 548
• DOI: 10.1039/c7ce00279c
• Languages: English
• ISSNs: 1466-8033

Abstract

Abstract : Selective adsorption of surfactants was theoretically predicted on crystal faces to prepare well-dispersed nanoparticles for the self-assembly of a high-quality stable dielectric constant film. Abstract : Well dispersed single-crystalline BaTiO3 nanoparticles with controlled morphologies were synthesized using a thermohydrolysis route. The nanoparticles were tuned from spherical to cubic upon changing the NaOH concentration under a critical molar ratio of oleic acid to hydrazine. Density functional theory (DFT) and molecular dynamics (MD) calculations indicated that hydrazine molecules adsorbed preferably on the Ti position of the Ti–O terminated surface; meanwhile, oleic acid molecules tended to adsorb on the Ba position of the Ba–O terminated surface. The added hydrazine changed the formation mechanism of BaTiO3 nanoparticles from an in situ growth to a dissolution–precipitation growth. Excellent dispersibility in aqueous solution was achieved for the BaTiO3 nanoparticles under the assistance of hydrazine. Meanwhile, a high-quality self-assembled film with a stable dielectric constant of 30 in the frequency range from 0 Hz to 1 MHz was prepared using the well dispersed BaTiO3 nanoparticles, providing a novel low-temperature route for the fabrication of perovskite films.