Hybrid
perovskite photovoltaics combine high performance with the
ease of solution processing. However, to date, a poor understanding
of morphology formation in coated perovskite precursor thin films
casts doubt on the feasibility of scaling-up laboratory-scale solution
processes. Oblique slot jet drying is a widely used scalable method
to induce fast crystallization in perovskite thin films, but deep
knowledge and explicit guidance on how to control this dynamic method
are missing. In response, we present a quantitative model of the drying
dynamics under oblique slot jets. Using this model, we identify a
simple criterion for successful scaling of perovskite solution printing
and predict coating windows in terms of air velocity and web speed
for reproducible fabrication of perovskite solar cells of ∼15%
in power conversion efficiencyin direct correlation with the
morphology of fabricated thin films. These findings are a corner stone
toward scaling perovskite fabrication from simple principles instead
of trial and error optimization.
We report on the fabrication of condensed and mesoporous silica coated CoFe2O4 and FeCo alloy magnetic nanocomposites. The CoFe2O4 magnetic nanoparticles were encapsulated by well defined silica layer with a uniform thickness of 5 nm. The mesoporous silica shells lead to a larger magnetic coercivity than that of the pure CoFe2O4 magnetic nanoparticles due to decrease of interparticle interactions and magneto-elastic anisotropy. In addition, the FeCo nanoparticles were coated with condensed and mesoporous silica. As a consequence, the condensed silica protects the reactive FeCo alloy from oxidation up to 300 °C, maintaining the high magnetization of the nanoparticles. However, saturation magnetization of silica coated FeCo nanoparticles is dramatically decreased after annealing at 400 °C due to the oxidation of the FeCo core.
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