RIKEN Center for Emergent Matter Science, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan.
Department of Chemistry and Biotechnology, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.
Nat Commun. 2020 Nov 27;11(1):6026. doi: 10.1038/s41467-020-19905-4.
Although various biomimetic soft materials that display structural hierarchies and stimuli responsiveness have been developed from organic materials, the creation of their counterparts consisting entirely of inorganic materials presents an attractive challenge, as the properties of such materials generally differ from those of living organisms. Here, we have developed a hydrogel consisting of inorganic nanosheets (14 wt%) and water (86 wt%) that undergoes thermally induced reversible and abrupt changes in its internal structure and mechanical elasticity (23-fold). At room temperature, the nanosheets in water electrostatically repel one another and self-assemble into a long-periodic lamellar architecture with mutually restricted mobility, forming a physical hydrogel. Upon heating above 55 °C, the electrostatic repulsion is overcome by competing van der Waals attraction, and the nanosheets rearrange into an interconnected 3D network of another hydrogel. By doping the gel with a photothermal-conversion agent, the gel-to-gel transition becomes operable spatiotemporally on photoirradiation.
虽然已经开发出各种具有结构层次和刺激响应性的仿生软材料,但完全由无机材料组成的相应材料的创造仍然是一个具有吸引力的挑战,因为这些材料的性质通常与生物体不同。在这里,我们开发了一种由无机纳米片(14wt%)和水(86wt%)组成的水凝胶,其内部结构和机械弹性发生热诱导的可逆和突然变化(23 倍)。在室温下,水中的纳米片相互排斥并自组装成具有相互限制的流动性的长周期层状结构,形成物理水凝胶。当加热到 55°C 以上时,静电斥力被竞争的范德华吸引力所克服,纳米片重新排列成另一种水凝胶的相互连接的 3D 网络。通过在凝胶中掺杂光热转换剂,凝胶到凝胶的转变可以通过光照射在空间和时间上进行操作。