Abstract

We present two new synthetic routes for bismuth ferrite harmonic nanoparticles (BiFeO3 HNPs). Both phase-pure and mixed phase BiFeO3 materials were produced after improvement of the solvent evaporation and sol-gel combustion routes. Metal nitrates with a series of dicarboxylic acids (tartronic, tartaric and mucic) were used to promote crystallization. We found that the longer the carbon backbone with a hydroxyl group attached to each carbon, the lower the annealing temperature. We also demonstrate that nanocrystals more readily formed at a given temperature by adding glycerol but to the detriment of phase purity, whereas addition of NaCl in excess with mucic acid promotes the formation of phase-pure, monocrystalline nanoparticles. This effect was possibly associated with a better dispersion of the primary amorphous precursors and formation of intermediate complexes. The nanoparticles have been characterized by XRD, TEM, ζ-potential, photon correlation spectroscopy, two-photon microscopy and Hyper-Rayleigh Scattering measurements. The improved crystallization leads to BiFeO3 HNPs without defect-induced luminescence and with a very high averaged second harmonic efficiency (220 pm/V), almost triple the efficiency previously reported. This development of simple, scalable synthesis routes which yield phase-pure and, crucially, monocrystalline BiFeO3 HNPs demonstrates a significant advance in engineering the properties of nanocrystals for bio-imaging and diagnostics applications.

Details

Title
Preparation from a revisited wet chemical route of phase-pure, monocrystalline and SHG-efficient BiFeO3 nanoparticles for harmonic bio-imaging
Author
Clarke, Gareth 1 ; Rogov, Andrii 2 ; McCarthy, Sarah 3   VIAFID ORCID Logo  ; Bonacina, Luigi 2   VIAFID ORCID Logo  ; Yurii Gun’ko 3 ; Galez, Christine 4 ; Ronan Le Dantec 4 ; Volkov, Yuri 5 ; Mugnier, Yannick 4   VIAFID ORCID Logo  ; Prina-Mello, Adriele 6   VIAFID ORCID Logo 

 Department of Clinical Medicine, Trinity Translational Medicine Institute (TTMI), Trinity College Dublin, Dublin 8, Ireland; CRANN Institute and AMBER centre, Trinity College Dublin, Dublin 2, Ireland; Univ. Savoie Mont Blanc, SYMME, Annecy, France 
 GAP – Biophotonics, Université de Genève, Genève 4, Switzerland 
 CRANN Institute and AMBER centre, Trinity College Dublin, Dublin 2, Ireland; School of Chemistry, Trinity College Dublin, Dublin 2, Ireland 
 Univ. Savoie Mont Blanc, SYMME, Annecy, France 
 Department of Clinical Medicine, Trinity Translational Medicine Institute (TTMI), Trinity College Dublin, Dublin 8, Ireland; CRANN Institute and AMBER centre, Trinity College Dublin, Dublin 2, Ireland; Department of Histology, Cytology and Embryology, First Moscow State Sechenov Medical University, Moscow, Russian Federation 
 Department of Clinical Medicine, Trinity Translational Medicine Institute (TTMI), Trinity College Dublin, Dublin 8, Ireland; CRANN Institute and AMBER centre, Trinity College Dublin, Dublin 2, Ireland 
Pages
1-10
Publication year
2018
Publication date
Jul 2018
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2068344792
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.