Waste-Free Fully Electrically Fueled Dissipative Self-Assembly System

被引:21
作者
Barpuzary, Dipankar [1 ,2 ]
Hurst, Paul J. [2 ]
Patterson, Joseph P. [1 ,3 ,4 ]
Guan, Zhibin [1 ,3 ,4 ]
机构
[1] Univ Calif Irvine, Ctr Complex & Act Mat, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Biomol Chem, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Chem, Dept Mat Sci & Engn, Dept Chem & Biomol Engn, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
基金
美国国家科学基金会;
关键词
INTRAMOLECULAR ELECTRON-TRANSFER; METHYL VIOLOGEN; DRIVEN; FLOW;
D O I
10.1021/jacs.2c13140
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The importance and prevalence of energy-fueled active materials in living systems have inspired the design of synthetic active materials using various fuels. However, several major limitations of current designs remain to be addressed, such as the accumulation of chemical wastes during the process, unsustainable active behavior, and the lack of precise spatiotem-poral control. Here, we demonstrate a fully electrically fueled (e-fueled) active self-assembly material that can overcome the aforementioned limitations. Using an electrochemical setup with dual electrocatalysts, the anodic oxidation of one electrocatalyst (ferrocyanide, [Fe(CN)6]4-) creates a positive fuel to activate the self-assembly, while simultaneously, the cathodic reduction of the other electrocatalyst (methyl viologen, [MV]2+) generates a negative fuel triggering fiber disassembly. Due to the fully catalytic nature for the reaction networks, this fully e-fueled active material system does not generate any chemical waste, can sustain active behavior for an extended period when the electrical potential is maintained, and provides spatiotemporal control.
引用
收藏
页码:3727 / 3735
页数:9
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