微尺度化学
活性物质
灵活性(工程)
纳米技术
自由度(物理和化学)
材料科学
胶体
生物系统
分子
计算机科学
化学物理
物理
工程类
化学工程
数学教育
统计
细胞生物学
生物
量子力学
数学
作者
Stefania Ketzetzi,Lorenzo Caprini,Vivien Willems,Laura Alvarez,Hartmut Löwen,Lucio Isa
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-08-11
卷期号:19 (32): 29430-29439
被引量:1
标识
DOI:10.1021/acsnano.5c07142
摘要
Molecular machines and microorganisms employ dynamic shape changes to enable adaptive function. In contrast, active colloidal machines and micromotors, their synthetic counterparts, are typically preconfigured and mechanically rigid, which limits the range of their dynamic behavior and thereby their functionality. Here, through physical interactions alone, we assemble active colloidal molecules with flexible configurations that evolve freely and continuously in time. Unlike existing colloidal systems that either offer structural flexibility in passively diffusing assemblies, or impose fixed configurations in self-propelling ones, our colloidal molecules both dynamically self-assemble and disassemble on demand and directly propel themselves through their own internal restructuring. This, in turn, bestows enhanced self-regulation, self-steering, and avoiding capabilities upon encountering other molecules. These capabilities suppress clustering and motility-induced phase separation, allowing them to remain dispersed, well-separated, and still actively moving even at high concentrations. Micromotors with dynamic configurational freedom thus constitute a step toward autonomous motion beyond classical synthetic active matter, and allow for designing "intelligent" microrobots and responsive functional active materials at the nano- and microscale.
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