The nucleation, growth, and orientation of lead zirconate titanate thin films prepared from organometallic precursor solutions by spin coating on (111) oriented platinum substrates and crystallized by rapid thermal annealing was investigated. The effects of pyrolysis temperature, post-pyrolysis thermal treatments, and excess lead addition are reported. The use of post-pyrolysis oxygen anneals at temperatures in the regime of 350-450 °C was found to strongly affect the kinetics of subsequent amorphous-pyrochlore-perovskite crystallization by rapid thermal annealing. The use of such post-pyrolysis anneals allowed films of reproducible microstructure and textures [both (100) and (111)] to be prepared by rapid thermal annealing. It is proposed that such anneals and pyrolysis temperature affect the oxygen concentration/average Pb valence in the amorphous films prior to annealing. Such changes in the Pb valence state then affect the stability of the transient pyrochlore phase and thus the kinetics of perovskite crystallization.
Extremely high magnetoresistance (XMR) in the lanthanum monopnictides LaX (X = Sb, Bi) has recently attracted interest in these compounds as candidate topological materials. However, their perfect electron-hole compensation provides an alternative explanation, so the possible role of topological surface states requires verification through direct observation. Our angle-resolved photoemission spectroscopy (ARPES) data reveal multiple Dirac-like surface states near the Fermi level in both materials. Intriguingly, we have observed circular dichroism in both surface and near-surface bulk bands. Thus the spin-orbit coupling-induced orbital and spin angular momentum textures may provide a mechanism to forbid backscattering in zero field, suggesting that surface and near-surface bulk bands may contribute strongly to XMR in LaX. The extremely simple rock salt structure of these materials and the ease with which high-quality crystals can be prepared suggests that they may be an ideal platform for further investigation of topological matter.
We report here a new versatile method to deposit discrete hydroxyapatite
(HA) nanoparticles on a titanium (Ti) implant with predisposing substrate
microtopography, which exhibited an unexpectedly robust biological effect.
Commercially pure Ti substrates were treated with 3-aminopropyltriethoxysilane,
on which HA nanoparticles (20 nm) were deposited and chemically bonded to
TiO2. The HA deposition rate was linearly related to the treatment time and HA nanoparticles
were deposited on up to 50% of the substrate surface. As a result, the discrete deposition of
HA nanoparticles generated novel 20–40 nm nanotopography on the Ti substrate with
microtopography that was smooth (turned) or roughened by double acid etching (DAE).
The experimental implants with or without HA nanoparticles were surgically placed in rat
femur and an implant push-in test was performed after two weeks of healing. The
deposition of HA nanoparticles on the DAE surface increased the mechanical withstanding
load by 129% and 782% as compared to the control DAE and turned implants, respectively.
Micro-computed tomography-based 3D bone morphometry revealed equivalent
bone volumes around the DAE implant with or without HA nanoparticles. These
data suggest that the discrete deposition of HA nanoparticles accelerates the
early osseointegration process, likely through increased shear bonding strengths.
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