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Updated: Feb 8, 2026

Nanosponge Tunability in Size and Crosslinking Density
Published on: August 4, 2017
Morphology control of shell-crosslinked polymer particles prepared by photo-induced shell-selective crosslinking
Yukiya Kitayama1, Toshifumi Takeuchi1
1Graduate School of Engineering, Kobe University, 1-1, Rokkodai-cho, Nada-ku, Kobe 657-8501, Japan.
Hypothesis:
Morphology control of polymer particles is of great importance for creating functional particulate materials. Photoinduced shell-selective crosslinking approach with spherical polymer particles has been previously developed in a dispersed state, in which the polymer particles could rotate freely, yielding hollow polymer particles after removal of non-crosslinked polymers because photoinduced crosslinking occurred for the entire particle surface. This insight prompted the question of whether non-spherical particles can be obtained if particle rotation is restricted and photoirradiation occurs for only part of the shell region.
Experiments:
Herein, we developed a facile approach for morphology control of polymer particles prepared by photoinduced shell-selective crosslinking of spherical polymer particles bearing photoreactive cinnamoyl groups by regulating the dispersed state. The morphology of the polymer particles obtained from the photo-induced shell-selective crosslinking approach in dispersed or non-dispersed states was confirmed. In-situ real time observation of forming the non-spherical polymer particles was also performed by optical microscope.
Findings:
Hollow and bowl-shaped polymer particles were successfully obtained from same spherical polymer particles bearing photo-crosslinking groups in dispersed and non-dispersed states, respectively. The versatility of the approach was confirmed by using various comonomers. Furthermore, post-functionalization for the polymer particles was also successfully performed using functional groups derived from the comonomers.
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