“Cation exchange mediated elimination of the Fe-antisites in the hydrothermal synthesis of LiFePO4”. Paolella A, Bertoni G, Hovington P, Feng Z, Flacau R, Prato M, Colombo M, Marras S, Manna L, Turner S, Van Tendeloo G, Guerfi A, Demopoulos GP, Zaghib K;, Nano energy 16, 256 (2015). http://doi.org/10.1016/j.nanoen.2015.06.005
Abstract: In this work we elucidate the elimination of mechanism Fe-antisite defects in lithium iron phosphate (LiFePO4) during the hydrothermal synthesis. Compelling evidence of this effect is provided by combining Neutron Powder Diffraction (NPD), High Resolution (Scanning) Transmission Electron Microscopy (HR-(S)TEM), Electron Energy Loss Spectroscopy (EELS), X-Ray Photoelectron Spectroscopy (XPS) and calculations. We found: i) the first intermediate vivianite inevitably creates Fe-antisite defects in LiFePO4; ii) the removal of these antisite defects by cation exchange is assisted by a nanometer-thick amorphous layer, rich in Li, that enwraps the LiFePO4 crystals.
Keywords: A1 Journal article; Engineering sciences. Technology; Electron microscopy for materials research (EMAT)
Impact Factor: 12.343
Times cited: 27
DOI: 10.1016/j.nanoen.2015.06.005
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“Epitaxial CdSe-Au nanocrystal heterostructures by thermal annealing”. Figuerola A, van Huis M, Zanella M, Genovese A, Marras S, Falqui A, Zandbergen HW, Cingolani R, Manna L, Nano letters 10, 3028 (2010). http://doi.org/10.1021/nl101482q
Keywords: A1 Journal article; Electron microscopy for materials research (EMAT)
Impact Factor: 12.712
Times cited: 112
DOI: 10.1021/nl101482q
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“Accelerated removal of Fe-antisite defects while nanosizing hydrothermal LiFePO4 with Ca2+”. Paolella A, Turner S, Bertoni G, Hovington P, Flacau R, Boyer C, Feng Z, Colombo M, Marras S, Prato M, Manna L, Guerfi A, Demopoulos GP, Armand M, Zaghib K;, Nano letters 16, 2692 (2016). http://doi.org/10.1021/acs.nanolett.6b00334
Abstract: Based on neutron powder diffraction (NPD) and high angle annular dark field scanning transmission electron microscopy (HAADF-STEM), we show that calcium ions help eliminate the Fe-antisite defects by controlling the nucleation and evolution of the LiFePO4 particles during their hydrothermal synthesis. This Ca-regulated formation of LiFePO4 particles has an overwhelming impact on the removal of their iron antisite defects during the subsequent carbon coating step since (i) almost all the Fe-antisite defects aggregate at the surface of the LiFePO4 crystal when the crystals are small enough and (ii) the concomitant increase of the surface area, which further exposes the Fe-antisite defects. Our results not only justify a low-cost, efficient and reliable hydrothermal synthesis method for LiFePO4 but also provide a promising alternative viewpoint on the mechanism controlling the nanosizing of LiFePO4, which leads to improved electrochemical performances.
Keywords: A1 Journal article; Engineering sciences. Technology; Electron microscopy for materials research (EMAT)
Impact Factor: 12.712
Times cited: 30
DOI: 10.1021/acs.nanolett.6b00334
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“Fe2+Deficiencies, FeO Subdomains, and Structural Defects Favor Magnetic Hyperthermia Performance of Iron Oxide Nanocubes into Intracellular Environment”. Lak A, Cassani M, Mai BT, Winckelmans N, Cabrera D, Sadrollahi E, Marras S, Remmer H, Fiorito S, Cremades-Jimeno L, Litterst FJ, Ludwig F, Manna L, Teran FJ, Bals S, Pellegrino T, Nano letters 18, 6856 (2018). http://doi.org/10.1021/acs.nanolett.8b02722
Abstract: Herein, by studying a stepwise phase transformation of 23 nm FeO-Fe3O4 core-shell nanocubes into Fe3O4, we identify a composition at which the magnetic heating performance of the nanocubes is not affected by the medium viscosity and aggregation. Structural and magnetic characterizations reveal the transformation of the FeO-Fe3O4 nanocubes from having stoichiometric phase compositions into Fe2+ deficient Fe3O4 phases. The resultant nanocubes contain tiny compressed and randomly distributed FeO sub-domains as well as structural defects. This phase transformation causes a tenfold increase in the magnetic losses of the nanocubes, which remains exceptionally insensitive to the medium viscosity as well as aggregation unlike similarly sized single-phase magnetite nanocubes. We observe that the dominant relaxation mechanism switches from Néel in fresh core-shell nanocubes to Brownian in partially oxidized nanocubes and once again to Néel in completely treated nanocubes. The Fe2+ deficiencies and structural defects appear to reduce the magnetic energy barrier and anisotropy field, thereby driving the overall relaxation into Néel process. The magnetic losses of the particles remain unchanged through a progressive internalization/association to ovarian cancer cells. Moreover, the particles induce a significant cell death after being exposed to hyperthermia treatment. Here, we present the largest heating performance that has been reported to date for 23 nm iron oxide nanoparticles under cellular and intracellular conditions. Our findings clearly demonstrate the positive impacts of the Fe2+ deficiencies and structural defects in the Fe3O4 structure on the heating performance under cellular and intracellular conditions.
Keywords: A1 Journal article; Engineering sciences. Technology; Electron microscopy for materials research (EMAT)
Impact Factor: 12.712
Times cited: 51
DOI: 10.1021/acs.nanolett.8b02722
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