• Bistervels, Marloes H.
• Noorduin, Willem
• Schoenmaker, Hinco
• Brouwer, Albert Manfred
• Hoogendoorn, Niels T.
• Kamp, Marko

Abstract

Nature's intricate biominerals inspire fundamental questions on self-organization and guide innovations towards functional materials. While advances in synthetic self-organization have enabled many levels of control, generating complex shapes remains difficult. Specifically, controlling morphologies during formation at the single micro/nanostructure level is the key challenge. Here, we steer the self-organization of barium carbonate nanocrystals and amorphous silica into complex nanocomposite morphologies by photogeneration of carbon dioxide (CO 2 ) under ultraviolet (UV) light. Using modulations in the UV light intensity, we select the growth mode of the self-organization process inwards or outwards to form helical and coral-like morphologies respectively. The spatiotemporal control over CO 2 photogeneration allows formation of different morphologies on pre-assigned locations, switching between different growth modes—to form for instance a coral on top of a helix or vice versa , and subtle sculpting and patterning of the nanocomposites during formation. These findings advance the understanding of these versatile self-organization processes and offer new prospects for tailored designs of functional materials using photochemically driven self-organization.

Topics

• nanocomposite
• impedance spectroscopy
• amorphous
• Carbon
• Barium