posted on 2022-07-05, 19:05authored byWeiguang Zhu, Yanming Zhang, Junhua Shen, Yunfeng Shi, Mingxin Li, Jie Lian
Manipulating
materials at the atomic scale and assembling them
into macroscopic structures with controlled dimensionalities and single-crystal
quality are grand scientific challenges. Here, we report a general
solvent evaporation method to synthesize large-area uniaxial-oriented
growth of free-standing thin films at the liquid–air interface.
Crystals nucleate at the solution surface and rotate into the same
orientation under electrostatic interaction and then merge as large
crystals and grow laterally into a large-area uniform thin film with
millimeter-sized grains. The lateral dimension is confined only by
the size of containers. The film thickness can be tuned by adjusting
solvent evaporation rate (R) and solute diffusivity
(D), and a characteristic length, L*∼DR, was derived to estimate the film thickness.
Molecular dynamic (MD) simulations reveal a concentration spike at
the liquid–air interface during fast solvent evaporation, leading
to the lateral growth of thin films. The large-area uniaxial oriented
films are demonstrated on both inorganic metal halides and hybrid
metal halide perovskites. The solvent evaporation approach and the
determination of key parameters enabling film thickness prediction
are beneficial to the high throughput and scalable production of single
crystal-quality thin film materials under controlled evaporation conditions.