TY - JOUR
T1 - Nano-confined crystallization of organic ultrathin nanostructure arrays with programmable geometries
AU - Gao, Hanfei
AU - Qiu, Yuchen
AU - Feng, Jiangang
AU - Li, Shuang
AU - Wang, Huijie
AU - Zhao, Yuyan
AU - Wei, Xiao
AU - Jiang, Xiangyu
AU - Su, Yewang
AU - Wu, Yuchen
AU - Jiang, Lei
PY - 2019/9/2
Y1 - 2019/9/2
N2 - Fabricating ultrathin organic semiconductor nanostructures attracts wide attention towards integrated electronic and optoelectronic applications. However, the fabrication of ultrathin organic nanostructures with precise alignment, tunable morphology and high crystallinity for device integration remains challenging. Herein, an assembly technique for fabricating ultrathin organic single-crystal arrays with different sizes and shapes is achieved by confining the crystallization process in a sub-hundred nanometer space. The confined crystallization is realized by controlling the deformation of the elastic topographical templates with tunable applied pressures, which produces organic nanostructures with ordered crystallographic orientation and controllable thickness from less than 10 nm to ca. 1 μm. The generality is verified for patterning various typical solution-processable materials with long-range order and pure orientation, including organic small molecules, polymers, metal-halide perovskites and nanoparticles. It is anticipated that this technique with controlling the crystallization kinetics by the governable confined space could facilitate the electronic integration of organic semiconductors.
AB - Fabricating ultrathin organic semiconductor nanostructures attracts wide attention towards integrated electronic and optoelectronic applications. However, the fabrication of ultrathin organic nanostructures with precise alignment, tunable morphology and high crystallinity for device integration remains challenging. Herein, an assembly technique for fabricating ultrathin organic single-crystal arrays with different sizes and shapes is achieved by confining the crystallization process in a sub-hundred nanometer space. The confined crystallization is realized by controlling the deformation of the elastic topographical templates with tunable applied pressures, which produces organic nanostructures with ordered crystallographic orientation and controllable thickness from less than 10 nm to ca. 1 μm. The generality is verified for patterning various typical solution-processable materials with long-range order and pure orientation, including organic small molecules, polymers, metal-halide perovskites and nanoparticles. It is anticipated that this technique with controlling the crystallization kinetics by the governable confined space could facilitate the electronic integration of organic semiconductors.
UR - https://www.scopus.com/pages/publications/85071647325
U2 - 10.1038/s41467-019-11883-6
DO - 10.1038/s41467-019-11883-6
M3 - Article
C2 - 31477721
AN - SCOPUS:85071647325
SN - 2041-1723
VL - 10
JO - Nature Communications
JF - Nature Communications
M1 - 3912
ER -